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Skelly AC, Chou R, Dettori JR, et al. Integrated and Comprehensive Pain Management Programs: Effectiveness and Harms [Internet]. Rockville (MD): Agency for Healthcare Research and Quality (US); 2021 Oct. (Comparative Effectiveness Review, No. 251.)

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Integrated and Comprehensive Pain Management Programs: Effectiveness and Harms [Internet].

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Appendix BResults Overview

Results of Literature Searches

Figure B-1 is a literature flow diagram that shows 20,558 records were identified through database searching. After these 20,558 abstracts were screened for inclusion, 10,858 records were excluded and 9,700 full-text articles were assessed for eligibility. Of these 9,700 articles, 9,252 were excluded. 26 were excluded for an ineligible population; 207 were excluded for an ineligible intervention or comparator; 25 were excluded for an ineligible outcome; 66 were excluded for an ineligible study design; 12 were excluded for an ineligible publication type; 2 articles were excluded for being in a foreign language; and 32 were excluded for an ineligible or outdated systematic review. The other 78 full-text articles encompassed 57 included RCTs in the 78 publications. Of the 78 included publications, 8 RCTs in 11 publications evaluated integrated pain management program and 49 RCTs in 67 publications evaluated comprehensive pain management programs.

Figure B-1Literature flow diagram

a Cochrane databases include the Cochrane Central Register of Controlled Trials and the Cochrane Database of Systematic Reviews

b Studies checked for inclusion.

A total of 10,953 references were identified, 10,782 from electronic database searches and an additional 76 from handsearching and checking the bibliographies of included studies and systematic reviews, and 95 from peer review/public comment. After dual review of abstracts, 509 articles were evaluated for inclusion at the full-text level. A total of 57 randomized controlled trials (RCTs) (in 78 publications) met inclusion criteria and were included for Key Questions 1 and 2 addressing effectiveness and safety. Forty-three were rated fair quality (75%) and 14 (25%) were rated poor quality. Search results and selection of studies are summarized in the literature flow diagram above (Figure B-1). A list of included studies appears in Appendix D and excluded studies with reason for exclusion in Appendix H.

Table B-1Number of studies overall and by Key Question

ProgramComparator

KQ1:

n=Number of RCTs (Number of Publications)

KQ2:

n=Number of RCTs (Number of Publications)

Total:

n=Number of RCTs (Number of Publications)

IPMP Usual care or waitlist7 (10)2029NANA
Provider vs. patient programNA120NA
Program with and without online supportNA130NA
Any7 (10)2029220,308 (11)2030
CPMP Usual care or waitlist23 (30)3160NANA
Physical activity15 (21)33,34,38,45,46,4850,6173NANA
Psychological therapy5 (6)38,45,46,48,60,74NANA
Pharmacologic therapy5 (13)7587NANA
Pharmacologic therapy plus physical activity2 (3)80,81,88NANA
Program total hours (greater vs. fewer)NA4 (7)33,34,43,62,63,89,90NA
Program setting (inpatient vs. outpatient)NA4 (6)41,42,55,58,59,70NA
Program components (with vs. without additional psychological or physical components)NA356,91,92NA
Preintervention assessment (with vs. without)NA293,94NA
Session format (group vs. individual)NA190NA
Booster sessions (with vs. without)NA172NA
Other comparisonsaNA2 (3)95,96NA
Any41 (58)3155,578816 (22)33,34,4143,55,56,58,59,62,63,70,72,899749 (67)3197
IPMP and CPMP Any48 (68)2029,3155,578818 (24)20,30,33,34,4143,55,56,58,59,62,63,70,72,899757 (78)2097

CPMP = comprehensive pain management program; IPMP = integrated pain management program; KQ = Key Question; NA = not applicable; RCT = randomized controlled trial.

a

Comparisons included a function-centered vs. a pain-centered approach to CPMP in one trial and an “exposure in vivo” approach vs. a graded activity approach to CPMP in the other trial.

Description of Included Studies

Tables B-2 and B-3 below provide an overview of the trial and population characteristics for RCTs that address Key Questions 1 (effectiveness and safety) and 2 (program factors), respectively. Data for trials evaluating integrated pain management programs (IPMPs) and comprehensive pain management programs (CPMPs) are presented separately. Weighted mean or proportions are presented for all IPMP or CPMP trials and then for these programs versus each specific comparator.

Table B-2Study and population characteristics for trials addressing KQ1 by type of program and comparator

Weighted Means or Proportionsa

IPMP

All Comparisons

IPMP

Vs. UC/WL

IPMP

Vs. PT, Psychological Therapyb

CPMP

All Comparisons

CPMP

Vs. UC/WL

CPMP

Vs. PA Alone

CPMP

Vs. Psychological Therapy Alone

CPMP

Vs. Pharmacologic Therapy Alone

CPMP

Vs. PA + Pharmacologic Therapy

N population 24842263397582327062363531311116
# of unique RCTs 771412315552
# publications 101025830216133
# RCTs conducted in United States 440331100
Mean age (years) (n trials) b 56.7 (6)56.8 (6)63.445.4 (35)45.8 (19)43.8 (11)45.5 (4)47.0 (4)47.3 (1)
% Male (n trials) 48% (7)50% (7)27%40% (40)36% (21)47% (14)38% (4)29% (4)0% (1)
% Disabled (n trials) 33% (6)36% (6)6%57% (19)71% (6)66% (7)62% (3)10% (2)23% (1)
% Nonwhite (n trials) 31% (4)31% (4)43%6% (8)7% (5)NR (0)NR (0)2% (1)NR (0)
Mean pain/disease duration, months (n trials) 153 (3)153 (3)NR (0)110 (23)123 (14)46 (6)95 (5)102 (4)196 (1)
Mean baseline pain score (0-10) (n trials) 5.3 (4)5.3 (4)NR (0)5.5 (25)4.9 (13)4.4 (7)5.4 (3)6.6 (3)4.5 (2)
% LBP 30%33%0%52%38%69%25%57%47%
% OA, RA 34%37%100%7%16%0%0%0%0%
% FM, CWP 18%10%0%16%21%7%0%43%53%
% Neck, shoulder pain 0%0%0%0%0%0%0%0%0%
% Mixed/multiple pain conditions 19%21%0%22%20%22%75%0%0%
% Other 0%0%0%3%7%18%0%0%0%
% Depression diagnosis (n trials) 18% (1)18% (1)0%20% (7)20% (6)18% (3)11% (1)NR (0)NR (0)
% Anxiety diagnosis (n trials) 13% (1)13% (1)0%32% (4)35% (5)22% (1)22% (1)NR (0)NR (0)
% PTSD diagnosis (n trials) 17% (1)17% (1)0%NR (0)NR (0)NR (0)NR (0)NR (0)NR (0)
% Overweight, obese (n trials) 56% (1)56% (1)0%77% (1)NR (0)NR (0)NR (0)NR (0)NR (0)
% SUD (n trials) NR (0)NR (0)NR (0)NR (0)NR (0)9% (1)14% (1)NR (0)NR (0)
% Suicidal ideation (n trials) NR (0)NR (0)NR (0)5% (2)9% (3)NR (0)NR (0)0% (1)0% (1)
% Smoking (n trials) NRNRNR34% (8)41% (3)45% (3)NR5% (2)NR (0)
# Fair-quality RCTs (% of total) 6 (86%)6 (86%)1 (100%)29 (71%)15 (65%)13 (87%)3 (60%)3 (60%)1 (50%)
# Poor-quality RCTs (% of total) 1 (14%)1 (14%)NA12 (29%)8 (35%)2 (13%)2 (40%)2 (40%)1 (50%)

CPMP = comprehensive pain management program; CWP = chronic widespread pain; FM = fibromyalgia; IPMP = Integrated Pain Management Programs; LBP = low back pain; NA = not applicable; NR = Not reported; OA = osteoarthritis; PTSD = post-traumatic stress disorder; RA = rheumatoid arthritis; SUD = substance use disorder

a

Some trials did not report the baseline demographic/characteristics listed. The weighted mean or proportion was calculated from the number of trials (i.e., n trials) that did report that variable

b

Data are for one trial with three arms

Table B-3Study and population characteristics for trials addressing KQ2 by type of program and comparator

Weighted Means or ProportionsaIPMP

CPMP

Higher Vs. Lower Hours

CPMP

IP Vs. OP Setting

CPMP

Addition of Components

CPMP

Preintervention Assessment

CPMP

Philosophical Approaches

CPMP

Booster Sessions

CPMP

Group Vs. Individualb

N population 51732855115842925923250
# of RCTs 24432211
# publications 27632311
# RCTs conducted in United States 10010000
Mean age (years) (n trials) 58.8 (2)42.2 (2)45.9 (2)41.4 (2)46.0 (1)43.0 (2)48.942.0
% Male (n trials) 32% (2)42% (2)57% (4)18% (2)54% (2)70%23%41%
% Disabled (n trials) 85 (1)58% (2)64% (1)100% (1)81% (1)54% (1)NRNR
% Non-White (n trials) 40% (1)NR (0)12% (2)NR (0)NRNR (0)NRNR
Mean pain or disease duration, months (n trials) 115 (2)90 (1)155 (2)74 (1)NR (0)108 (1)NR (0)NR (0)
Mean pain score at baseline (0-10) (n trials) 4.7 (2)5.9 (3)6.0 (3)4.6 (2)7.2 (1)5.5 (2)NR (0)NR (0)
% LBP 0%41%75%41%0%100%0%100%
% OA, RA 0%0%0%0%0%0%0%0%
% FM, CWP 0%12%0%0%0%0%0%0%
% Neck, shoulder pain 0%0%0%0%0%0%0%0%
% Mixed/multiple pain conditions 100%47%25%59%100%0%0%0%
% Other 0%0%0%0%0%0%100%c0%
% Depression diagnosis (n trials) NRNRNRNRNRNRNRNR
% Anxiety diagnosis (n trials) NRNRNRNRNRNRNRNR
% PTSD diagnosis (n trials) NRNRNRNRNRNRNRNR
% Overweight, obese (n trials) NRNRNRNRNRNRNRNR
% SUD (n trials) NRNRNRNRNRNRNRNR
% Suicidal ideation (n trials) NRNRNRNRNRNRNRNR
% Smoking NRNRNRNRNRNRNRNR
# Fair-quality RCTs (% of total) 2 (100%)3 (75%)02 (67%)2 (100%)2 (100%)1 (100%)0
# Poor-quality RCTs (% of total) 01 (25%)4 (100%)1 (33%)0001 (100%)

CPMP = comprehensive pain management program; CWP = chronic widespread pain; FM = fibromyalgia; IPMP = Integrated Pain Management Programs; LBP = low back pain; NR = Not reported; OA = osteoarthritis; PTSD = post-traumatic stress disorder; RA = rheumatoid arthritis; SUD = substance use disorder

a

Some trials did not report the baseline demographic/characteristics listed. The weighted mean or proportion was calculated from the number of trials (i.e., n trials) that did report that variable

b

Population demographics for this study include patients not included in this comparison; authors reported demographics for the population as a whole.

c

All patients included in this study had chronic back pain (at any location).

Summary Results Tables

Table B-4Summary results for trials addressing KQ1: IPMPs versus usual care, versus physical activity, and versus psychological therapy

Author, Year

Country

Pain Duration

Study Design

Study Quality

Intervention and Comparator (n): Duration/Intensity, Session Format, SettingPopulation

Primary Outcomes:

Pain, Function, and Opioid Use

Secondary Outcomes:

HRQOL, Psychological Measures, Global Improvement, Patient Satisfaction

Harms Utilization

Allen, 2016

USA

Mean duration of pain: 170 months

Cluster RCT

Fair

A. Patient focused multidisciplinary treatment + provider focused multidisciplinary treatment + usual care (n=151 patients, 15 providers): 12 months (time duration NR), individual, Community-based outpatient clinics

B. Usual care (n=149 patients, 15 providers)

Patient Participants

Mean age: 61 years

Male: 91%

Non-White race: 50%

Pain etiology/type: Arthritis

Joints with OA:

-

Knee only: 79%

-

Hip only: 11%

-

Knee and hip: 10%

Disabled: 33%

Fair or poor health: 38%

Mean BMI: 33.8 kg/m2

Provider Participants

Mean study patients per provider: 10.0

<15% females in patient panel: 83%

Male: 40%

Provider Type:

-

Physician: 63%

-

Physician Assistant: 23%

-

Nurse Practitioner: 10%

-

Registered Nurse: 3%

A vs. B, mean (SD)

WOMAC Pain Subscale (0-10)

Baseline: 5.1 (NR) (not reported by group)

Postintervention: 4.7 (NR) vs. 4.95 (NR), difference −0.25 (95% CI −0.6 to 0.1)

Estimated percentage improving ≥18% on WOMAC score from baseline (8.7 point reduction)

Postintervention: 36.1% (NR) vs. 28.2% (NR); OR 1.3 (95% CI, 0.9 to 1.8)

WOMAC Total (0-96)

Baseline: 48.9 (17.6) vs. 47.8 (17.4)

Postintervention: 44.4 (NR) vs. 48.5 (NR), difference −4.1 (95% CI −7.2 to −1.1)

WOMAC Function Subscale (0-68)

Baseline: 33.8 (NR) (not report by group)

Postintervention: 31.0 (NR) vs. 34.3 (NR), difference −3.3 (95% CI −5.7 to −1.0)

SPPB (Physical Function) (0-12)

Baseline: 8.0 (2.6) vs. 8.1 (2.5)

Postintervention: 7.8 (NR) vs. 7.6 (NR), difference 0.3 (95% CI −0.3 to 0.9)

A vs. B, mean (SD)

PHQ-8 (0-24)

Baseline: 7.2 (5.6) vs. 6.4 (5.1)

Postintervention: 6.2 (NR) vs. 6.8 (NR), difference −0.6 (95% CI −1.5 to 0.3)

A vs. B, % (n/N)

Adverse Events

4 study-related adverse events occurred, but none were associated with the OA intervention.

Provider Referrals Orthopedic visit:

-

Referral: 5.3% (8/151) vs. 6.0% (9/149)

-

Receipt: 50.0% (4/8) vs. 66.7% (6/9)

Allen, 2017

USA

Mean duration of symptoms: 124.8 months

Cluster RCT

Fair

A. Patient focused multidisciplinary treatment + provider focused multidisciplinary treatment + usual care (n=140 patients, 5 providers): 12 months (time duration NR), individual, Community-based outpatient clinics

B. Provider focused multidisciplinary treatment + usual care (n=140 patients, 5 providers): 12 months

C. Patient focused multidisciplinary treatment + usual care (n=128 patients, 5 providers): 12 months

D. Usual care (n=129 patients, 5 providers)

Patient Participants

Mean age: 63.3 years

Male: 26%

Non-White race: 40%

Joints with OA:

-

Knee only: 85%

-

Hip only: 9%

-

Knee and hip: 6%

Disabled: 8%

Fair or poor health: 20%

Mean BMI: 35.6 kg/m2

Clinic and Provider Characteristics

Mean providers: 7.3

Mean medical physicians and osteopaths: 6.2

Mean nurse practitioners and physician assistants: 1.1

Family medicine practice: 60%

Internal medicine practice: 40%

Providers:

-

Male: 38%

-

Mean years since graduation: 18.9 years

A vs. B vs. C vs. D, difference in change scores (95% CI) from baseline to follow-up

WOMAC Pain Subscale (0-10)

Baseline: 4.2 (NR) vs. 4.0 (NR) vs. 4.4 (NR) vs. 3.8 NR)

Postintervention: difference in change scores from baseline for

A vs. D: −0.15 (–0.65 to 0.3)

B vs. D: 0.15 (–0.35 to 0.6)

C vs. D: −0.2 (–0.7 to 0.25)

Estimated percentage (95% CI) improving ≥18% on WOMAC score from baseline (8.7 point reduction)

Postintervention: 44% (35% to 56%) vs. 35% (28% to 44%) vs. 49% (37% to 63%) vs. 49% (42% to 57%)

Only group B (provider) differed from group D (usual care): OR 0.7 (95% CI, 0.4 to 0.9), p = 0.016

WOMAC Total (0-96)

Baseline: 40.1 (15.8) vs. 37.7 (17.9) vs. 41.0 (15.9) vs. 35.6 (18.0)

Postintervention: difference in change scores from baseline for

A vs. D: −0.7 (–4.2 to 2.8)

B vs. D: 2.5 (–0.9 to 5.9)

C vs. D: −1.5 (–5.1 to 2.0)

WOMAC Function Subscale (0-68)

Baseline: 27.5 (NR) vs. 26.0 (NR) vs. 28.5 (NR) vs. 24.7

Postintervention: difference in change scores from baseline for

A vs. D: −0.2 (–2.7 to 2.3)

B vs. D: 2.3 (–0.1 to 4.7)

C vs. D: −1.0 (–3.5 to 1.6)

SPPB (Physical Function)

Baseline: 8.5 (NR) vs. 8.8 (NR) vs. 8.3 (NR) vs. 8.5 (NR)

Postintervention: difference in change scores from baseline for

A vs. D: −0.3 (–0.8 to 0.3)

B vs. D: −0.4 (–1.0 to 0.1)

C vs. D: −0.3 (–0.8 to 0.3)

A vs. B vs. C vs. D, difference in change scores (95% CI) from baseline to follow-up

PHQ-8 score (0-24)

Baseline (mean, SD): 4.9 (NR) vs. 4.5 (NR) vs. 4.8 (NR) vs. 4.0 (NR)

Postintervention: difference in change scores from baseline for

A vs. D: 0.1 (–0.8 to 1.0)

B vs. D: 0.6 (–0.2 to 1.5)

C vs. D: 0.3 (–0.6 to 1.2)

A vs. B vs. C vs. D, % (n/N)

Harms

No study-related adverse events occurred

Joint Injection:

-

16.7% (17/102) vs. 22.9% (27/118) vs. 23.7% (22/93) vs. 18.5% (19/103)

New pain medication (medication not specified):

-

38.8% (40/103) vs. 33.1% (41/124) vs. 27.8% (27/97) vs. 28.8% (32/111)

Joint replacement surgery:
-

3.6% (5/139) vs. 2.1% (3/143) vs. 3.9% (5/128) vs. 3.1% (4/129)

A vs. B only, % (n/N) Table 5

Orthopedic Visit:

-

Recommended: 1.4% (2/140) vs. 3.6% (5/140)

-

Receipt: NR

Discuss new/alternative pain medication (medication not specified):
-

Recommended: 72.1% (101/140) vs. 76.4% (107/140)

-

Receipt: 33.7% (34/101) vs. 30.8% (33/107)

Angeles, 2013

Canada

Mean duration of pain: NR

RCT

Poor

A. IPMP (n=29) 2 months (2 hour group sessions 1 time per week) (16 hours total), group, Outpatient clinics

B. Waitlist (n=34):

40 to 59 years of age: 51% (mean age NR)

Male: 27%

Race/ethnicity: NR

Pain etiology/type: chronic MSK or neuropathic pain

-

work-related accident: 31%

-

non work-related accident: 27%

-

disease process: 60%

Currently taking medications for pain: 91%
-

Taken medications not prescribed by doctor (medication not specified): 37%

Receiving government compensation
-

before onset of pain: 8%

-

after onset of pain: 24%

A vs. B, % (n/N)

Early opioid prescription refill:

Intermediate term: 7.7% (1/19) vs. 25% (6/22), p=0.08; RR 0.19 (95% CI 0.03 to 1.46)

Increase in opioid medication dose:

Intermediate term: 11.5% (2/19) vs. 9.4% (2/22), p=0.56; RR 1.16 (95% CI 0.18 to 7.45)

A vs. B, Mean change (SD NR)

SF-36 PCS

Baseline: NR

Postintervention: change from baseline −2.9 vs. −3.0, p=0.98

SF-36 MCS

Baseline: NR

Postintervention: change from baseline 3.6 vs. 3.6, p=1.00

Harms

No study-related adverse events occurred.

Dobscha, 2008/2009 & Dickinson, 2010

USA

Mean duration of pain: 178 months

Cluster RCT

Fair

A. IPMP – provider assistance with pain treatment and use of stepped care (n=214): 12 months (time duration NR), mode of delivery NR, 3 urban and 2 rural outpatient clinics

B. Usual care (n=187)

Mean age: 62 years

Male: 92%

Race/Ethnicity

-

White: 89%

-

Black: 2%

-

American Indian/Alaska Native: 3%

-

Not reported: 6%

Pain etiology/type
-

Back pain: 67%

-

Neck or joint pain: 65% - Rheumatism, OA, or arthritis: 49%

-

Proportion of patients with >1 musculoskeletal condition: 66%

Disability
-

All patients scored ≥6 on RMDQ

-

Currently receiving disability payment: 65%

Comorbidities
-

Mean RxRisk-V (0-45): 4.9

-

Major depression diagnosis: 18%

-

Mean depression severity (0-27): 8.3

-

PTSD diagnosis: 16%

-

Anxiety syndrome: 13%

-

Panic attack within past 4 weeks: 17%

-

Positive AUDIT-C alcohol misuse screening: 16%

-

Endorses drug misuse in past 6 months: 3%

-

Reports prior substance use treatment: 16%

-

Taking antidepressant at study entry: 36%

-

Taking opioids 6 months prior to study entry: 43%

A vs. B, Mean (95% CI)

Chronic Pain Grade Severity/Intensity subscale (0–100) a

Baseline: 67.4 (65.4 to 69.3) vs. 66.0 (64.3 to 67.8)

Postintervention: : 63.2 (60.7 to 65.7) vs. 65.6 (63.3 to 67.9), difference −2.4 (95% CI −7.03 to 2.23)

Proportion of patients demonstrating a ≥30% reduction in RMDQ score

Postintervention: 21.9% (41/187) vs. 14.0% (30/214); RR 1.56 (95% CI 1.02 to 2.40)

RMDQ (0–24) a

Baseline: 14.6 (14.3 to 14.9) vs. 14.5 (14.0 to 15.0)

Postintervention: 13.3 (12.9 to 13.7) vs. 14.3 (13.6 to 15.0), difference −1.0 (95% CI −1.69 to −0.31)

Chronic Pain Grade Disability/Interference subscale (0–100) a

Baseline: 49.3 (45.9 to 52.8) vs. 48.7 (45.5 to 51.9)

Postintervention: 44.6 (40.7 to 48.4) vs. 51.1 (47.6 to 54.6), difference −6.5 (95% CI −11.74 to −1.26)

Pain disability-free days, Mean (SD)

Baseline to postintervention: 141.8 (108.3) vs. 124.1 (107.5), difference 17.7 (95% CI −3.54 to 38.94)

Medication prescriptions for a 52-week period, % (n/N) c

Any opioid prescribed: 65% (120/185) vs. 61% (129/212)

-

If opioid prescribed, any that is long acting: 31% (37/120) vs. 18% (23/129)

A vs. B, Mean (95% CI)

EQ-5D (0-1) a

Baseline: 0.65 (0.63 to 0.68) vs. 0.64 (0.62 to 0.67)

Postintervention: 0.64 (0.61 to 0.67) vs. 0.60 (0.57 to 0.63), difference 0.04 (95% CI – 0.002 to 0.08)

PHQ-9 (0-27) b

Baseline: 14.4 (13.4 to 15.5) vs. 14.4 (13.5 to 15.3)

Postintervention: 10.6 (9.1 to 12.1) vs. 13.2 (11.9 to 14.5), difference −2.6 (95% CI −4.61 to 0.59)

Global treatment satisfaction (scale NR) a

Baseline: 2.9 (2.8 to 3.0) vs. 2.9 (2.8 to 3.1)

Postintervention: 2.7 (2.5 to 2.8) vs. 2.6 (2.4 to 2.7), difference 0.1 (95% CI −0.11 to 0.31)

Global impression of change in past 6 months (0-7)

Postintervention: 3.7 (3.5 to 3.8) vs. 4.4 (4.3 to 4.6), difference −0.7 (95% CI −0.93 to −0.47)

A vs. B, Mean (SD) or % (n/N)

Harms

No study-related adverse events occurred.

Healthcare Utilization

-

Any mental health appointment: 45% (83/185) vs. 28% (59/212)

-

Any substance use disorder appointment: 0.5% (1/185) vs. 0.5% (1/212)

-

Any pain specialty consultation service appointment: 7% (13/185) vs. 3% (6/212)

-

Any orthopedic or neurosurgery appointment: 16% (30/185) vs. 13% (28/212)

-

Any emergency department visit: 30% (56/185) vs. 30% (64/212)

-

Any inpatient admission: 12% (22/185) vs. 13% (28/212)

Mas, 2019

Spain

Mean duration of pain: 0.5 to 3 months

Cluster RCT

Fair

A. IPMP (n=262; 26 primary healthcare centers): one 10 hour session (4 hours physical therapy, 4 hours psychology, 2 hours for questions with general practitioner (10 hours total), combined group and individual, outpatient clinic

B. Usual Care (n=239; 13 primary healthcare centers)

Mean age: 47 years

Male: 35%

Race/Ethnicity: NR

Pain etiology/type:

Subacute low back pain

Disability: NR

Comorbidities:

-

Obese: 17%

-

Overweight: 39%

A vs. B, Mean (SD or 95% CI)

MPQ VAS pain (0–10)

Baseline: 5.8 (2.3) vs. 5.9 (2.3)

Short term: 3.2 (3.2) vs. 4.1 (3.3), adjusted difference −0.77 (95% CI −1.53 to −0.01)

Long term (12 months): 3.6 (3.0) vs. 3.9 (3.2), adjusted difference −0.27 (95% CI – 0.88 to 0.34)

MPQ Total Intensity Score (0–14) d

Baseline: 6.7 (3.1) vs. 6.5 (3.1)

Short term: 4.0 (3.6) vs. 4.6 (3.6), adjusted difference −0.49 (–1.39 to 0.42)

Long term (12 months): 3.1 (3.2) vs. 3.6 (3.6), adjusted difference 0.69 (–1.41 to 0.02)

MPQ Current Intensity Score (0-5)

Baseline: 2.6 (1.1) vs. 2.5 (1.2)

Short term: 1.7 (1.5) vs. 1.3 (1.4), adjusted difference −0.32 (95% CI −0.63 to −0.02)

Long term (12 months): 1.6 (1.4) vs. 1.4 (1.3), adjusted difference −0.18 (95% CI – 0.43 to 0.08)

RMDQ (0-24)

Baseline: 10.0 (5.2) vs. 9.9 (5.3)

Short term: 6.2 (4.9) vs. 7.4 (5.5), adjusted difference −1.33 (95% CI −2.22 to −0.45)

Long term (12 months): 5.1 (4.9) vs. 6.0 (5.7), adjusted difference −1.11 (95% CI – 2.08 to −0.13)

A vs. B, Mean (SD)

SF-12 Physical health (0-100)

Baseline: 41.9 (9.0) vs. 40.7 (9.3)

Short term: 46.5 (8.7) vs. 45.3 (9.8), adjusted difference 0.55 (95% CI −1.19 to 2.29)

Long term (12 months): 47.0 (8.9) vs. 46.2 (9.5), adjusted difference 0.53 (95% CI −1.20 to 2.27)

SF-12 Mental health (0-100)

Baseline: 43.4 (12.8) vs. 42.3 (12.4)

Short term: 48.8 (12.0) vs. 45.0 (13.2), adjusted difference 2.56 (95% CI −0.33 to 5.45)

Long term (12 months): 48.9 (11.2) vs. 47.0 (11.9), adjusted difference 1.48 (95% CI −0.86 to 3.83)

NR

McBeth 2012 & Beasley, 2015

England

Mean duration of pain: NR

RCT

Fair

A. IPMP with telephone delivered CBT and exercise (n=112): 6 months, initial assessment (0.75 to 1 hour) seven weekly sessions for 6 weeks (0.5 to 0.75 hours per session, 3.5 to 5.25 hours each week, 21 to 31.5 hours over 6 weeks), and a single 0.5- to 0.75-hour session at 3 and 6 months (0.5 to 1.5 hours) (21.25 to 34.75 hours total), individual, patient home and local gym

B. Usual Care (n=109)

C. Telephone-delivered CBT alone (n=112)

D. Exercise alone (n=109)

Mean age: 56 years

Male: 31%

Race/Ethnicity: NR

Pain etiology/type: Chronic widespread pain

Disability: NR

Comorbidities:

-

Patients with severe psychiatric disorders were excluded

% (n/N)

Chronic Pain Grade questionnaire

A vs. B

Baseline:

-

0: 0% (0/112) vs. 0% (0/109)

-

I: 25.9% (29/112) vs. 17.4% (19/109)

-

II: 43.8% (49/112) vs. 51.4% (56/109)

-

III: 22.3% (25/112) vs. 16.5% (18/109)

-

IV: 8.0% (9/112) vs. 14.7% (16/109)

Postintervention:
-

0: 0% (0/76) vs. 0% (0/88)

-

I: 60.5% (46/76) vs. 41.2% (28/68)

-

II: 31.6% (24/76) vs. 47.1% (32/68)

-

III: 5.3% (4/76) vs. 7.4% (5/88)

-

IV: 2.6% (2/76) vs. 4.4% (3/68)

RR 1.04 (95% CI 0.92 to 1.16)

Short term:

-

0: 0% (0/71) vs. 0% (0/76)

-

I: 54.9% (39/71) vs. 35.5% (27/76)

-

II: 31.0% (22/71) vs. 52.6% (40/76)

-

III: 11.3% (8/71) vs. 4.0% (3/76)

-

IV: 2.8% (2/71) vs. 7.9% (6/76)

RR 0.97 (95% CI 0.86 to 1.10)

Long term (24 months):

-

0: 13.5% (10/74) vs. 19.4% (14/72)

-

I: 39.2% (29/74) vs. 25.0% (18/72)

-

II: 28.4% (21/74) vs. 30.6% (22/72)

-

III: 10.8% (8/74) vs. 15.3% (11/72)

-

IV: 8.1% (6/74) vs. 9.7% (7/72)

RR 1.08 (95% CI 0.91 to 1.29)

A vs. C

Baseline:

-

0: 0% (0/112) vs. 0% (0/112)

-

I: 25.9% (29/112) vs. 21.4% (24/112)

-

II: 43.8% (49/112) vs. 47.3% (53/112)

-

III: 22.3% (25/112) vs. 20.5% (23/112)

-

IV: 8.0% (9/112) vs. 10.7% (12/112)

Postintervention:
-

0: 0% (0/76) vs. 0% (0/58)

-

I: 60.5% (46/76) vs. 44.8% (26/58)

-

II: 31.6% (24/76) vs. 36% (21/58)

-

III: 5.3% (4/76) vs. 17.2% (10/58)

-

IV: 2.6% (2/76) vs. 1.7% (1/58)

RR 1.14 (95% CI 0.99 to 1.31)

Short term:

-

0: 0% (0/71) vs. 1.7% (1/58)

-

I: 54.9% (39/71) vs. 46.6% (27/58)

-

II: 31.0% (22/71) vs. 31.0% (18/58)

-

III: 11.3% (8/71) vs. 10% (6/58)

-

IV: 2.8% (2/71) vs. 3.5% (2/58)

RR 1.01 (95% CI 0.87 to 1.17)

Long term (24 months):

-

0: 13.5% (10/74) vs. 18.2% (12/66)

-

I: 39.2% (29/74) vs. 33.3% (22/66)

-

II: 28.4% (21/74) vs. 30.3% (20/66)

-

III: 10.8% (8/74) vs. 12.1% (8/66)

-

IV: 8.1% (6/74) vs. 6.1% (4/66)

RR 0.99 (95% CI 0.85 to 1.16)

A vs. D

Baseline:

-

0: 0% (0/112) vs. 0% (0/109)

-

I: 25.9% (29/112) vs. 23.9% (26/109)

-

II: 43.8% (49/112) vs. 45.9% (50/109)

-

III: 22.3% (25/112) vs. 18.4% (20/109)

-

IV: 8.0% (9/112) vs. 11.9% (13/109)

Postintervention:
-

0: 0% (0/76) vs. 0% (0/76)

-

I: 60.5% (46/76) vs. 43.4% (33/76)

-

II: 31.6% (24/76) vs. 44.7% (34/76)

-

III: 5.3% (4/76) vs. 10.5% (8/76)

-

IV: 2.6% (2/76) vs. 1.3% (1/76)

RR 1.04 (95% CI 0.94 to 1.16)

Short term:

-

0: 0% (0/71) vs. 47.3% (35/74)

-

I: 54.9% (39/71) vs. 44.6% (33/74)

-

II: 31.0% (22/71) vs. 8.1% (6/74)

-

III: 11.3% (8/71) vs. 0% (0/74)

-

IV: 2.8% (2/71) vs. 3.0% (2/74)

RR 0.88 (95% CI 0.80 to 0.97)

Long term (24 months):

-

0: 13.5% (10/74) vs. 14.1% (10/71)

-

I: 39.2% (29/74) vs. 32.4% (23/71)

-

II: 28.4% (21/74) vs. 22.5% (16/71)

-

III: 10.8% (8/74) vs. 21.1% (15/71)

-

IV: 8.1% (6/74) vs. 9.9% (7/71)

RR 1.18 (95% CI 0.97 to 1.42)

Mean (SD)

SF-36 PCS (0-100)

A vs. B

Baseline: 38.1 (8.0) vs. 37.4 (8.2)

Postintervention: 43.0 (9.2) vs. 39.9 (10.1), difference 3.1 (95% CI 0.54 to 5.66)

Short term: 42.8 (9.9) vs. 39.6 (10.5), difference 3.2 (95% CI 0.49 to 5.91)

Long term (24 months): NR

A vs. C

Baseline: 38.1 (8.0) vs. 38.9 (8.4)

Postintervention: 43.0 (9.2) vs. 41.5 (11.0), difference 1.5 (95% CI −1.17 to 4.17)

Short term: 42.8 (9.9) vs. 40.8 (11.2), difference 2.0 (95% CI −0.78 to 4.78)

Long term (24 months): NR

A vs. D

Baseline: 38.1 (8.0) vs. 37.8 (7.5)

Postintervention: 43.0 (9.2) vs. 40.2 (10.1), difference 2.8 (95% CI 0.24 to 5.36)

Short term: 42.8 (9.9) vs. 41.9 (9.1), difference 0.9 (95% CI −1.62 to 3.42)

Long term (24 months): NR

SF-36 MCS (0-100)

A vs. B

Baseline: 43.9 (10.0) vs. 42.5 (10.6)Postintervention: 46.0 (10.9) vs. 43.4 (10.2), difference: 2.6 (95% CI −0.20 to 5.4)

Short term: 45.5 (10.6) vs. 43.4 (11.0), difference 2.1 (95% CI −0.76 to 4.96)

Long term (24 months): NR

A vs. C

Baseline: 43.9 (10.0) vs. 43.6 (10.9)

Postintervention: 46.0 (10.9)vs. 46.3 (9.9), difference −0.3 (95% CI −3.04 to 2.44)

Short term: 45.5 (10.6) vs. 47.0 (10.2), difference −1.5 (95% CI −4.24 to 1.24)

Long term (24 months): NR

A vs. D

Baseline: 43.9 (10.0) vs. 43.5 (10.1)

Postintervention: 46.0 (10.9) vs. 46.7 (10.8), difference −0.7 (95% CI −3.58 to 2.18)

Short term: 45.5 (10.6) vs. 45.8 (9.7), difference −0.3 (95% CI −2.99 to 2.40)

Long term (24 months): NR

GHQ (0-12)

A vs. B

Baseline: 3.1 (3.5) vs. 3.4 (3.5)

Postintervention: 1.7 (2.8) vs. 2.8 (3.5), difference −1.1 (95% CI −1.94 to −0.26)

Short term: 2.0 (3.4) vs. 3.0 (3.8), difference −1.0 (95% CI −1.96 to −0.05)

Long term (24 months): 3.0 (3.7) vs. 3.0 (3.3), difference 0.0 (95% CI −0.93 to 0.93)

A vs. C

Baseline: 3.1 (3.5) vs. 3.3 (3.6) Postintervention: 1.7 (2.8) vs. 1.7 (2.9), difference: 0.0 (95% CI −0.75 to 0.75)

Short term: 2.0 (3.4) vs. 2.0 (3.6), difference 0.0 (95% CI −0.92 to 0.92)

Long term (24 months): 3.0 (3.7) vs. 2.2 (3.4), difference 0.8 (–0.14 to 1.74)

A vs. D

Baseline: 3.1 (3.5) vs. 3.2 (3.6)

Postintervention: 1.7 (2.8) vs. 1.8 (2.8), difference −0.1 (95% CI −0.84 to 0.64)

Short term: 2.0 (3.4) vs. 2.0 (3.0), difference 0.0 (95% CI −0.85 to 0.85)

Long term (24 months): 3.0 (3.7) vs. 2.6 (3.7), difference 0.4 (95% CI −0.581 to 1.38)

EQ-5D (0-1)

Long term (24 months):

A vs. B

0.68 (0.24) vs. 0.63 (0.32), difference 0.05 (95% CI −0.02 to 0.13)

A vs. C

0.68 (0.24) vs. 0.73 (0.24), difference −0.05 (95% CI – 0.11 to 0.01)

A vs. D

0/68 (0.24) vs. 0.71 (0.24), difference −0.03 (95% CI −0.09 to 0.03)

Clinical global impression change score (0-7, higher=greater feeling of change in health status; Much better or very much better = scores of 6 and 7; Less than much better = scores <6

A vs. B

Postintervention:

-

Much better or very much better: 37.2% (35/94) vs. 8.1% (7/87)

-

Less than much better: 62.8% (59/94) vs. 91.9% (80/88); RR 4.63 (95% CI 2.17 to 9.87)

Short term:
-

Much better or very much better: 37.1% (36/101) vs. 8.3% (8/98)

-

Less than much better: 64.4% (65/101) vs. 91.8% (90/101); RR 4.37 (95% CI 2.14 to 8.92)

Long term (24 months):
-

Much better or very much better: 31.2% (29/93) vs. 12.8% (12/94), adjusted OR 2.9 (95% CI 1.4 to 6.0)

-

Less than much better: 68.8% (64/93) vs. 87.2% (82/94); RR 2.44 (95% CI 1.33 to 4.50)

A vs. C

Postintervention:

-

Much better or very much better: 37.2% (35/94) vs. 29.9% (26/87)

-

Less than much better: 62.8% (59/94) vs. 70.1% (61/87); RR 1.25 (95% CI 0.82 to 1.89)

Short term:
-

Much better or very much better: 37.1% (36/101) vs. 32.6% (29/91)

-

Less than much better: 64.4% (65/101) vs. 67.4% (60/91); RR 1.12 (95% CI 0.75 to 1.67)

Long term (24 months):
-

Much better or very much better: 31.2% (29/93) vs. 35.4% (29/82)

-

Less than much better: 68.8% (64/93) vs. 64.6% (53/82); RR 0.88 (95% CI 0.58 to 1.34)

A vs. D

Postintervention:

-

Much better or very much better: 37.2% (35/94) vs. 34.8% (32/92)

-

Less than much better: 62.8% (59/94) vs. 65.2% (60/92); RR 1.07 (95% CI 0.73 to 1.57)

Short term:
-

Much better or very much better: 37.1% (36/101) vs. 24.2% (24/99)

-

Less than much better: 64.4% (65/101) vs. 75.8% (75/99); RR 1.47 (95% CI 0.95 to 2.27)

Long term (24 months):
-

Much better or very much better: 31.2% (29/93) vs. 29.3% (27/92)

-

Less than much better: 68.8% (64/93) vs. 70.7% (65/92); RR 1.06 (95% CI 0.69 to 1.65)

Harms

Two deaths due to cancer were recorded: (1 in the exercise group and 1 in the TCBT group). None of the adverse events were due to the interventions.

Von Korff, 2005

USA

Mean duration of pain: NR

USA

Fair

A. IPMP (n=119 randomized): 4 sessions over ~1 month, one 1.5 hour psychology session during first visit, then one 1 hour physical therapy session 1 to 1.5 weeks later, followed by a 0.5 hour psychology session 2 weeks later, and then a 0.5 hour physical therapy session 1.5 weeks later (3.5 hours total), individual, outpatient

B. Usual Care (n=121 randomized): NR

Mean age: 50 years

Male: 38%

Race/Ethnicity:

-

White race (not Hispanic): 83%

Pain etiology/type: Low back pain

Disability:

-

Receiving worker’s compensation or disability payments for back pain: 4%

-

Kept from usual activities for ≥30 days in prior 3 months: 29%

Chronic Pain Grade
-

Grade I (low pain intensity): 20%

-

Grade II (high pain intensity with low activity limitations): 20%

-

Grade III (moderate activity limitations): 24%

-

Grade IV (severe activity limitations): 36%

Comorbidities:
-

Prior back surgery for pain: 13%

A vs. B, Mean (SD)

Pain NRS (0-10)

Baseline: 5.7 (1.8) vs. 5.8 (1.8)

Postintervention: 4.9 (2.0) vs. 5.3 (1.9), difference: −0.4 (95% CI −0.90 to 0.10)

Short term: 4.2 (2.0) vs. 4.7 (2.2), difference: −0.5 (95% CI −1.04 to 0.04)

Intermediate term: 4.0 (2.3) vs. 4.7 (2.1), difference: −0.7 (95% CI −1.26 to −0.14)

Long term (24 months): 4.3 (2.1) vs. 4.6 (2.5), difference: −0.3 (95% CI −0.89 to 0.29)

RMDQ (0-23)

Baseline: 12.3 (5.5) vs. 11.4 (5.7)

Postintervention: 10.2 (6.3) vs. 11.5 (5.8), difference: −1.3 (95% CI −2.84 to 0.24)

Short term: 9.2 (6.6) vs. 10.1 (6.4), difference: −0.9 (95% CI −2.55 to 0.75)

Intermediate term: 8.4 (7.0) vs. 9.1 (6.3), difference: −0.7 (95% CI −2.39 to 0.99)

Long term (24 months): 8.1 (6.5) vs. 9.1 (7.2), difference: −1.0 (95% CI −2.75 to 0.75)

A vs. B, % (n/N)

Proportion of patients with greater than a one-third reduction in RMDQ score

Postintervention: 27.7% (28/101) vs. 13.2% (14/106), adjusted OR 3.9, p=0.0007

Short term: 42.2% (43/101) vs. 23.7% (25/106), adjusted OR 3.5, p=0.0005

Intermediate term: 44.6% (45/101) vs. 22.7% (24/106), adjusted OR 2.1, p=0.03

Long term (24 months): 49.4% (50/101) vs. 37.0% (39/106), adjusted OR 1.8, p=0.08

A vs. B, Mean (SD)

SF-36 Social functioning subscale (0-100)

Baseline 66.7 (26.7) vs. 70.4 (27.0)

Postintervention: NR

Short term: 74.4 (27.1) vs. 73.6 (27.8), difference: 0.8 (95% CI −6.18 to 7.78)

Intermediate term: 75.8 (28.3) vs. 74.4 (24.0), difference: 1.4 (95% CI −5.27 to 8.07)

Long term (24 months): 76.7 (25.2) vs. 76.3 (25.8), difference: 0.4 (95% CI −6.09 to 6.89)

SF-36 MCS (0-100)

Baseline 67.0 (18.3) vs. 68.9 (16.9)

Postintervention: NR

Short term: 70.3 (19.9) vs. 69.5 (19.1), difference: 0.8 (95% CI −4.16 to 5.76)

Intermediate term: 70.9 (19.9) vs. 71.1 (18.4), difference: −0.2 (95% CI −5.09 to 4.67)

Long term (24 months): 71.0 (18.2) vs. 72.4 (18.3), difference: −1.4 (95% CI −6.04 to 3.24)

A vs. B, % (n/N)

Proportion receiving workers compensation or disability payments for back pain

Baseline: 4.4% vs. 3.3%, p=NR

Postintervention: 1.8% vs. 4.2%, p=0.04

Short term: 4.6% vs. 4.6%, p=0.45

Intermediate term): 7.1% vs. 3.1%, p=0.53

Long term (24 months): 6.4% vs. 5.4%, p=0.67

Adverse Events

No study-related adverse events occurred.

BMI = Body mass index; CI = confidence interval; EQ5D = EuroQoL 5 dimensions; GHQ = General Health Questionnaire; HRQOL = Health-related quality of life; MCS = Mental Component Score; MPQ = McGill Pain Questionnaire; NR = not reported; NRS = numerical rating scale; OA = osteoarthritis; OMPSQ = Orebro Musculoskeletal Pain Screening Questionnaire; OR = odds ratio; PCS = Physical Component Score; PDI = Pain Disability Index; PHQ-8 or -9 = Patient Health Questionnaire 8 or 9 questions; RCT = randomized controlled trial; RMDQ = Roland Morris Disability Questionnaire; RR = risk ratio; SD = standard deviation; SF-12 = Short-Form 12; SF-36 = Short-Form 36 questionnaire; SPPB = Short Physical Performance battery; USA = United States of America; VAS = visual analog scale; WOMAC = Western Ontario and McMaster Universities Osteoarthritis Index

a

Adjusted for age, sex, PHQ-9 score at baseline, RxRisk-V medical morbidity score, and opioid prescription at any point from 6 months before, up to, and including enrollment date.

b

Adjusted for age, sex RxRisk-V medical morbidity, and opioid prescription withing 6 months prior to the enrollment date.

c

Adjusted for age, sex Patient Health Questionnaire 9 score at baseline, RxRisk-V medical morbidity, and baseline opioid prescription status.

d

Adjusted for age, gender, baseline outcome measurement, and the significant confounder and significant interaction variables.

Table B-5Summary results for trials addressing KQ1: CPMPs versus usual care or waitlist control

Author, Year

Country

Pain Duration

Study Design

Study Quality

Intervention and Comparator (n), Duration/Intensity, Session Format, SettingPopulationPrimary Outcomes: Pain, Function, and Opioid UseSecondary Outcomes: HRQOL, Psychological Measures, Global ImprovementHarms, Utilization, Patient Satisfaction

Abbasi, 2012

Iran

Duration of pain: 74 months

RCT

Poor

A. Comprehensive, pain management program, spouse assisted group (n=9): 1 day a week for 7 weeks, (2-hour sessions, 14 hours total) group sessions; outpatient

B. Comprehensive pain management program, conventional group (n=10): 1 day a week for 7 weeks, (2-hour sessions, 14 hours total) group sessions; outpatient

C. Usual care (n=10)

Mean age: 45 years

Male: 12%

Race/Ethnicity: NR

Median duration of pain: 74 months

Pain etiology/type: Chronic LBP

Disability: NR

Comorbidities:

-

Patients with major cognitive dysfunction or coexisting psychiatric morbidity were excluded

A vs. B vs. C, Mean (SD)

VAS pain in last week (0-10)

A vs. C

Baseline: 5 (2.7) vs. 3.6 (1.7)

Postintervention: 3 (1.8) vs. 3.2 (1.6), difference −0.20 (95% CI −1.80 to 1.40)

Long term: 2.8 (2.7) vs. 4.3 (1.4); difference −1.50 (95% CI −3.55 to 0.55)

B vs. C

Baseline: 4.6 (2) vs. 3.6 (1.7)

Postintervention: 2.6 (2) vs. 3.2 (1.6); difference −0.60 (95% CI −2.18 to 0.98)

Long term: 3.7 (2.5) vs. 4.3 (1.4); difference −0.60 (95% CI −2.50 to 1.30)

RMDQ (0-24)

A vs. C

Baseline: 11.2 (4.3) vs. 8.4 (3.3)

Postintervention: 5.8 (3) vs. 3.2 (3.2); difference 2.60 (95% CI −0.34 to 5.54)

Long term: 8.2 (5.4) vs. 10.4 (6.2); difference −2.20 (95% CI −7.86 to 3.46)

B vs. C

Baseline: 12.1 (5.7) vs. 8.4 (3.3)

Postintervention: 6.2 (4.4) vs. 3.2 (3.2); difference 3.00 (95% CI −0.36 to 6.36)

Long term: 8.8 (5.9) vs. 10.4 (6.2); difference −1.60 (95% CI −7.29 to 4.09)

NRNR

Ahlmen 1988

Sweden

Duration of pain: 11 years (≥10 years: 38%)

RCT

Fair

A. Comprehensive pain management program, Long-term (n=31): Duration of treatment: 12 months, 2 hours a week (14 hours total), individual + group sessions, outpatient

B. Usual care (n=28)

Mean age: 59 years

Female: 100%

Race/Ethnicity: NR

Pain etiology/type: Rheumatoid arthritis

Disability: NR

Comorbidities: NR

A vs. B, Mean (SD)

SIP Overall Score (0-100)

Baseline: 22.1 (11.8) vs. 19.8 (11.0)

Postintervention change score −3.6 (6.2) vs. −0.1 (5.3), p<0.05

SIP, Physical Index (scale NR)

Baseline: 22.7 (15.8) vs. 19.8 (13.1)

Postintervention change score: −4.6 (7.7) vs. 0.3 (5.5), p<0.01

SIP, Psychosocial Index (scale NR)

Baseline: 11.1 (7.8) vs. 11.2 (11.6)

Postintervention change score: −3.3 (7.1) vs. −0.7 (6.7), p=NS

A vs. B, Mean (SD)

MACL (scale NR)

Baseline: 3.28 (0.33) vs. 3.16 (0.46)

Postintervention: 3.29 (0.31) vs. 3.15 (0.44), p=NS

A vs. B, Mean (SD)

Utilization:

No between group differences in the following (data NR):

-

Drug treatment

-

Intraarticular corticosteroid injections

-

Orthopedic specialist consultations

-

Referral for inpatient rheumatologic care

Amris 2014 (IMPROvE trial)

Denmark

Duration of pain: median 126 months

RCT

Fair

A. Comprehensive pain management program (n=96): 2 weeks, (3 to 5 hours sessions, 35 hours total) group sessions; outpatient

B. Waitlist control (n=95)

Mean age: 44

Female: 100%

Race/Ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability:

-

Receiving disability pension at baseline: 12%

-

On sick leave: 16%

Comorbidities:
-

Patients with psychiatric disorders were excluded

A vs. B

Mean (95% CI) change scores from baseline

FIQ Pain VAS (0-10)

Baseline (mean, SD): mean 7.1 (2.0) vs 7.4 (1.7)

Short term: 0.07 (–0.31 to 0.44) vs. −0.14 (–0.52, 0.27), difference in change scores 0.21 (95% CI −0.32 to 0.74)

FIQ Total (0-100)

Baseline (mean, SD): 64.0 (15.8) vs 65.7 (13.0)

Short term: −1.28 (–3.90 to 1.33) vs. −1.37 (–4.01 to 1.28), difference in change scores 0.08 (95% CI −3.64 to 3.80)

A vs. B

% (n/N) or Mean (95% CI) change scores from baseline

Proportion of patients considered to be responders on the SF-36 PCS, % (n/N)

27% (26/96) vs. 23% (22/95), RR 1.16 (95% CI 0.72 to 1.91)

SF-36 PCS (0-100):

Baseline (mean, SD): 27.1 (6.9) vs 27.2 (7.0)

Short term: 1.35 (0.27 to 2.43) vs. 0.78 (−0.30 to 1.86), difference in change scores 0.57 (95% CI −0.95 to 2.1)

Proportion of patients considered to be responders on the SF-36 MCS, % (n/N)

27% (26/96) vs. 27% (26/95), RR 0.99 (95% CI 0.62 to 1.6)

A vs. B, Median (IQR) or Mean (95% CI)

SF-36 MCS (0-100)

Baseline (mean, SD): 39.4 (12.2) vs 37.8 (9.8)

Short term: 2.29 (0.41 to 4.18) vs. 1.15 (−0.73 to 3.03), difference in change scores 1.14 (95% CI −1.52 to 3.81)

Generalized Anxiety Disorder-10 (scale NR)

Baseline (median): 17.5 (IQR 13 to 26) vs 17.0 (IQR 13 to 23)

Short term: −0.78 (–2.01 to 0.46) vs. – 0.54 (–1.80 to 0.72), difference in change scores −0.24 (95% CI −2.00 to 1.53)

Major Depression Inventory (scale NR)

Baseline (median): 18.0 (IQR 13 to 27) vs 21.0 (IQR 15 to 27)

Short term: −1.73 (–3.19 to −0.27) vs. – 0.47 (–1.96 to 1.01), difference in change scores −1.26 (95% CI −3.34 to 0.82)

NR

Basler, 1997

Germany

Duration of pain: 129.6 months

RCT

Fair

A. Comprehensive pain management (n=36) 12 weeks (one 2.5-hour sessions per week) patients attended an outpatient review appointment (2-4 hours) at 1 and 3 months postdischarge group sessions, outpatient

B. Usual Care (n=40)

Mean age: 49 years

% Male: 24%

Race/ethnicity: NR

Pain etiology/type: Chronic LBP

Quebec Task Force on Spinal Disorders:

-

73% chronic pain syndrome

-

26% post-surgical spinal or radicular pain

Disability: NR
-

70% unemployed

-

90.4% considered significantly disabled

-

69% unemployed

Other characteristics:
-

Spinal surgery: 1.3%

-

Days using an opioid pain medication per week, mean (SD): 3.02 (2.85) vs. 3.41 (2.76)

A vs. B, Mean (SD)

VAS (0-10)

Baseline: 4.58 (1.77) vs. 3.99 (1.02)

Postintervention 4.08 (2.11) vs. 4.18 (1.37), difference −0.10 (95% CI −0.91 to 0.71)

Short term: 3.71 (2.01) vs. NR

Days without pain per week

Baseline: 0.30 (1.11) vs. 0.26 (0.92)

Postintervention: 0.58 (1.54) vs. 0.28 (0.85); difference 0.30 (95% CI −0.26 to 0.86)

Short term: 0.93 (2.04) vs. NR

Dusseldorf Disability Scale - physical function (0-5)

Baseline: 1.98 (0.92) vs. 1.84 (0.64)

Postintervention: 1.63 (0.87) vs. 1.84 (0.62); difference −0.21 (95% CI −0.55 to 0.13)

Short term: 1.44 (0.82) vs. NR

Days with pain medication per week

Baseline: 3.02 (2.85) vs. 3.41 (2.76)

Postintervention: 2.59 (2.91) vs. 3.23 (2.90); difference −0.64 (95% CI −1.97 to 0.69)

Short term: 2.34 (2.86) vs. NR

NRNR

Bendix, 1996, 1998a, 1998b (PROJECT A)

Denmark

Mean duration of pain: NR (≥6 months)

RCT

Fair

A. Comprehensive pain management program (n=55):

3 weeks full time (39 hours/week), then 1 day weekly for 3 additional weeks patients participated in a 6-hour followup program) group sessions, outpatient

B. Usual care (n=51)

Median age:

-

Group A: 41 years

-

Group B: 40 years

% Male: 30%

Race/ethnicity: NR

Pain etiology/type: Chronic LBP

Disability: NR

Comorbidities:

-

Smoker: 56%

-

Prior back surgery: 17%

A vs. B, median (IQR)

Back pain VAS (0-10)

Baseline (median): 6.1 vs. 6.1

Short term (mean, SD): 5.7 (4.1) vs. 6.9 (2.2), difference −1.20 (95% CI −2.54 to 0.14)

Long term (24 months) (mean, SD): 6.0 (3.7) vs. 6.5 (2.2), difference −0.50 (95% CI −1.70 to 0.70)

Long term (60 months) (mean SD): 5.0 (2.2) vs. 5.0 (1.8), difference 0 (95% CI −0.84 to 0.84)

Patient subjective disability due to back pain (0-30)

Baseline (median): 16.9 vs. 15.9

Short term: 12.1 (7.2 to 16.8) vs. 16.8 (13.1 to 20.1), p<0.001

Long term (24 months): 16.0 (8 to 19) vs. 15.0 (11 to 18), p=0.9

Long term (60 months): 12.0 (NR) vs. 16.0 (NR), p=0.2

A vs. B, Median (IQR)

Leg pain VAS (0-10)

Baseline (median): 4.1 vs. 4.6

Short term: 3.5 (0.3 to 7.0) vs. 5.4 (3.0 to 7.3), p=0.17

Long term (24 months): 4.5 (1.0 to 7.0) vs. 4.0 (1.0 to 7.0), p=0.90

Long term (60 months): 4.0 (NR) vs. 5.0 (NR), p=0.60

NR

A vs. B, % (n/N)

Proportion of patients taking prescription pain medications (opioids not specified)

Baseline: 80% (36/45) vs. 73% (36/49), p=0.39

Short term: NR

Long term (24 months): 72% (36/50) vs. 56% (27/49), p=0.20

Long term (60 months): NR

Proportion of patients hospitalized due to low back pain, % (n/N)

Short term: NR

Long term (24 months): NR

Long term (60 months): 22% (10/46) vs. 38% (16/42), p=0.09

Proportion of patients who underwent back surgery during the study period, % (n/N)

4 months: NR

24 months: NR

60 months: 7% (3/46) vs. 12% (5/42), p=0.40

Browne, 2013

Australia

Duration of pain: 1 month

RCT

Poor

A. Comprehensive pain management program (n=69):

Duration of treatment unclear (2.5 hours/week; 20 hours total) individual sessions; outpatient

B. Usual care (n=73)

Mean age: 37 years

% Male: 75%

Race/Ethnicity:

-

Caucasian: 92%

-

Asian: 4%

-

Indigenous: 4%

Pain etiology/type: Traumatic injury

Mechanism of injury

-

MVA/MBA: 73%

-

Fall: 8%

-

Assault: 7%

-

Sports related: 6%

-

Work related: 4%

-

Other 1%

Length of hospital stay: 13.87 days

Injury Severity Score: 9.6

Disability: NR

Comorbidities: NR

Mental Health History: 19%

Pain Medications at discharge:

-

slow release opioids (i.e., MS Contin, Kapanol, Oxycontin, Methadone, Fentanyl): 27%

-

antineuropathic (Gabapentin, Pregabalin, Clonazepam, Amitryptaline): 1%

-

combination of above: 10%

A vs. B, Mean (SD)

BPI (0-10)

Baseline: 5.12 (2.26) vs. 5.48 (2.11)

Postintervention: 3.13 (2.03) vs. 3.03 (2.74), difference 0.10 (95% CI −1.06 to 1.26)

FIM (scale 18-126)

Baseline: NR

Postintervention: 122.73 (4.74) vs. 123.00 (3.91), difference −0.27 (95% CI −2.40 to 1.86)

A vs. B, Mean (SD)

CES-D (0-60)

Baseline: 16.56 (9.55) vs. 14.88 (11.23)

Postintervention: 17.40 (12.39) vs. 14.97 (11.48); difference 2.43 (95% CI −3.44 to 8.30)

A vs. B, % (n/N) *

Clinical Pain Diagnosis at 6 months (made by attending Pain Specialist, includes both nociceptive and neuropathic pain)

-

pain with no impairment: 34.6% (11/31) vs. 29% (10/35); RR 1.24 (95% CI 0.61 to 2.52)

-

pain with impairment: 46.2% (14/31) vs. 38.7% (14/35); RR 1.13 (95% CI 0.64 to 1.98)

ADL Impairment (yes)

Postintervention: 50.0% (16/31) vs. 45.2% (16/35); RR 1.13 (95% CI 0.69 to 1.86)

Walking Impairment (yes)

Postintervention: 56.0% (17/31) vs. 37.9% (13/35); RR 1.48 (95% CI 0.86 to 2.52)

*numerators back-calculated using % and denominator provided

NR

de Buck, 2005

The Netherlands

Duration of pain:

Group A.11.0 months

Group B. 19.5 months

RCT

Fair

A. Comprehensive pain management program (n=74):

Duration NR (average between 4 and 12 weeks) Individual or group sessions NR; outpatient

B. Usual care (n=66)

Median age:

-

Group A: 43 years

-

Group B: 44 years

% Male: 44%

Race/Ethnicity: NR

Median duration of disease:

-

Group A: 11.0 months

-

Group B: 19.5 months

Pain etiology/type: Mixed chronic pain
-

Rheumatoid arthritis: 50%

-

Ankylosing spondylitis, psoriatic arthritis, or reactive arthritis: 21%

-

Systemic lupus erythematosus, scleroderma: 29%

Disability:
-

Partial work disability benefit: 16.4%

-

Sick leave: 55%

-

Complete sick leave: 29%

Comorbidities:
-

Charlson index ≥0: 43%

A vs. B, Mean (95% CI) change scores from baseline

VAS (0-10)

Baseline (mean, SD): 4.37 (2.31) vs. 4.71 (2.27)

Intermediate term change: −0.70 (95% CI −1.40 to 0.01) vs. −0.20 (95% CI −0.81 to −0.41)

Long term (12 months) change: −0.31 (95% CI −1.08 to 0.47) vs. −0.58 (95% CI −1.28 to 0.13)

Long term (18 month) change: −0.43 (95% CI −1.19 to 0.32) vs. −0.33 (95% CI −1.00 to 0.34)

Long term (24 month) change: −0.59 (95% CI −1.28 to 0.09) vs. −0.42 (95% CI −1.16 to 0.32)

HAQ (0-3)

Baseline (mean, SD): 0.76 (0.50) vs. 0.83 (0.55)

Intermediate term change: 0.03 (95% CI −0.08 to 0.13) vs. −0.04 (95% CI −0.16 to 0.08)

Long term (12 months) change: −0.04 (95% CI −0.15 to 0.06) vs. −0.07 (95% CI −0.19 to 0.05)

Long term (18 month) change: 0.00 (95% CI −0.11 to 0.11) vs. 0.08 (95% CI −0.04 to 0.21)

Long term (24 month) change: −0.01 (95% CI −0.14 to 0.12) vs. −0.10 (95% CI −0.23 to 0.03)

A vs. B, Mean (95% CI) change scores from baseline

RAND 36-item Health Survey PCS (0-100)

Baseline (mean, SD): 40.64 (17.66) vs. 43.32 (19.03)

Intermediate term change: 5.75 (95% CI −0.45 to 11.95) vs. 5.96 (95% CI 0.38 to 11.53)

Long term (12 months) change: 13.6 (95% CI 7.04 to 20.18) vs. 11.7 (95% CI 5.04 to 18.39)

Long term (18 month) change: 13.78 (95% CI 6.32 to 21.25) vs. 9.32 (95% CI 2.75 to 15.9)

Long term (24 month) change: 13.72 (95% CI 6.73 to 20.71) vs. 11.69 (95% CI 5.36 to 18.02)

RAND 36-item Health Survey MCS (0-100)

Baseline (mean, SD): 59.59 (24.08) vs. 64.10 (23.31)

Intermediate term change: −1.4 (95% CI −8.40 to 5.54) vs. 1.72 (95% CI −5.05 to 8.50)

Long term (12 months) change: 5.31 (95% CI −1.99 to 12.61) vs. 3.33 (95% CI −4.42 to 11.08)

Long term (18 month) change: 11.20 (95% CI 2.40 to 20.06) vs. 3.60 (95% CI −4.78 to 12.00)

Long term (24 month) change: 13.61 (95% CI 6.61 to 20.60) vs. 2.16 (95% CI −5.30 to 9.62)

HADS anxiety (0-21)

Baseline (mean, SD): 7.20 (4.00) vs. 6.80 (4.10)

Intermediate term change: −0.30 (95% CI −1.78 to 0.11) vs. −0.43 (95% CI −1.39 to 0.54)

Long term (12 months) change: −0.83 (95% CI −1.78 to 0.11) vs. −0.25 (95% CI −1.37 to 0.89)

Long term (18 month) change: −0.94 (95% CI −1.87 to −0.02) vs. −0.34 (95% CI −1.53 to 0.89)

Long term (24 month) change: −1.83 (95% CI −2.86 to −0.80) vs. −0.03 (95% CI −1.26 to 1.34)

HADS depression (0-21)

Baseline (mean, SD): 6.10 (3.30) vs. 5.70 (3.50)

Intermediate term change: −0.02 (95% CI −1.05 to 1.01) vs. 0.28 (95% CI −0.54 to 1.10)

Long term (12 months) change: −0.46 (95% CI −1.50 to 0.57) vs. 0.02 (–0.89 to 0.92)

Long term (18 month) change: −0.64 (95% CI −1.71 to 0.44) vs. −0.21 (95% CI −0.36 to 0.93)

Long term (24 month) change: −1.66 (95% CI −2.72 to −0.60) vs. 0.15 (95% CI −1.12 to 1.42)

NR

Härkäpää, 1989, 1990

Finland

Duration of pain:168 months

RCT

Poor

A. Comprehensive pain management program Inpatient group (n=156) 2 times a week for 2 months (15 sessions) (+ 2-week refresher sessions after 1.5 years) group sessions; inpatient

B. Comprehensive pain management program Outpatient group (n=150) 2 times a week for 2 months (15 sessions) (+ 8 refresher sessions after 1.5 years) group sessions; outpatient

C. Usual Care (n=153)

Mean age: 45 years

% Male: 63%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

-

Continuous LBP during past year: 41%

-

Severe LPB during past year: 81%

Other characteristics:
-

% Disability compensation, pensions: 10%

-

Use of opioid medication: NR

-

Use of analgesics: 65%

-

Work absenteeism due to LBP in past two years: 34%”

A vs. B vs. C, Mean (SD)

Pain Index (0-400)

Baseline: 184.9 (76.9) vs. 178.6 (81.8) vs. 175.8 (87.3)

Short term: 128 (NR) vs. 146 (NR) vs. 162 (NR)

Intermediate term: 158 (NR) vs. 160 (NR) vs. 154.5 (NR)

Long term (18 months): 156.5 (NR) vs. 174 (NR) vs. 161(NR)

Long term (22 months): 149 (NR) vs. 164 (NR) vs. 161.5 (NR)

Long term (30 months): 161.5 (NR) vs. 168 (NR) vs. 158.5 (NR)

LBP Disability Index (0-45)

Baseline: 16.7 (7.9) vs. 17.6 (7.4) vs. 16.7 (8.4)

Short term: 15.7 (NR) vs. 16 (NR) vs. 15.9 (NR)

Intermediate term: 15.7 (NR) vs. 16 (NR) vs. 15.9 (NR)

Long term (18 months): 15.55 (NR) vs. 17.05 (NR) vs.16.0 (NR)

Long term (22 months): 14.5 (NR) vs. 15.65 (NR) 15.65 vs. (NR)

Long term (30 months): 15.4 (NR) vs. 16.55 (NR) vs. 15.8 (NR)

A vs. B %, p-value

Benefits of treatment

Short term:

-

Increased knowledge concerning low back pains 88 vs. 84, p=NS

-

Increased knowledge of factors affecting low back pain: 81 vs. 77, p=NS

-

Increased motivation for self-care: 60 vs. 40, p=0.001

-

Decrease in low back pain: 57 vs. 38, p=0.05

-

Mental recreation: 56 vs. 25, p=0.001

-

Improved physical condition: 55 vs. 23, p=0.001

-

Improved working capacity: 45 vs. 22, p=0.01

-

Decrease in other illness symptoms: 24 vs. 10, p=0.02

NR

Jensen, 2001

Sweden

Duration of pain: 31 months

RCT

Fair

A. Comprehensive pain management program (n=63):

4 weeks*, (20 hours a week, 80 hours total) group sessions; outpatient

* (plus six 90-minute booster sessions over a period of 1 year after treatment)

B. Usual care (n=48)

Mean age: 43 years

% Male: 45%

Race/ethnicity:

-

Swedish origin: 67%

Pain etiology/type: Mixed chronic pain (long-term, nonspecific spinal pain)
-

Cervical/thoracic pain: 42%

-

Lumbar pain: 46%

-

Mixed pain areas: 12%

Disability: NR
-

Mean total sick leave in 6 months prior to inclusion in study: 292 (63)

Comorbidities: NR

NR

A vs. B, Mean (SD)

SF-36 Global health (scale 0-100)

Females only

A vs. B (n=30 vs. 28)

Baseline: 38.1 (14.5) vs. 45.6 (16.5)

Postintervention: 47.6 (18.0) vs. 47.0 (15.2); difference 0.60 (95% CI −8.12 to 9.40)

Intermediate term: 52.4 (21.6) vs. 46.3 (19.3); difference 6.10 (95% CI −4.70 to 16.90)

Long term (18 months): 53.1 (24.5) vs. 43.4 (20.1); difference 9.70 (95% CI – 2.14 to 21.5)

Males only

A vs. B (n=33 vs. 20)

Baseline: 41.6 (14.6) vs. 45.0 (14.7)

Postintervention: 48.5 (17.2) vs. 45.1 (13.2); difference 3.40 (95% CI −5.61 to 12.41)

Intermediate term: 54.3 (18.3) vs. 51.5 (24.2); difference 2.80 (95% CI −8.97 to 14.57)

Long term (18 months): 57.2 (21.8) 45.9 (21.2); difference 11.30 (95% CI −0.98 to 23.58)

A vs. B, Mean (SD)

Harms: NR

Perceived appropriateness of the treatment program to treating patient’s pain

Females only Postintervention: 6.4 (3.1) vs. NR

Males only Postintervention: 6.0 (3.6) vs. NR

Johansson, 1998

Norway

Duration of pain: 132 months

RCT

Fair

A. Comprehensive pain management program (n=21):

5 days a week for 5 weeks, (hours total NR) * group sessions; inpatient and outpatient

*(+ booster sessions after 2 months)

B. Waitlist control (n=21):

Mean age: 44 years

% Male: 22%

Race/ethnicity: NR

Pain etiology/type: Chronic musculoskeletal pain

Disability: NR

-

On sick leave: 75%

-

Unemployed: 32%

Comorbidities: NR
-

Patients with psychotic illness were excluded

A vs. B, Mean (SD)

VAS pain intensity (0-10)

Baseline: 5.28 (1.72) vs. 5.33 (1.84)

Postintervention: 4.93 (2.19) vs. 5.22 (2.19), difference −0.29 (95% CI −1.72 to 1.14)

Short term: 5.42 (2.42) vs. 5.32 (1.77), difference 0.10 (95% CI – 1.30 to 1.50)

VAS pain interference (0-10)

Baseline: 5.08 (1.85) vs. 4.69 (1.50)

Postintervention: 4.23 (2.23) vs. 4.82 (2.31), difference −0.59 (95% CI −2.13 to 0.95)

Short term: 4.76 (2.36) vs. 4.82 (1.72), difference −0.06 (95% CI – 1.45 to 1.33)

MPI general activity level (0-6)

Baseline: 2.8 (0.7) vs. 2.8 (0.7)

Postintervention: 3.0 (0.7) vs. 2.6 (0.7), difference 0.40 (95% CI −0.08 to 0.88)

Short term: 2.9 (0.7) vs. 2.4 (0.7), difference 0.50 (95% CI 0.03 to 0.98)

NRNR

Lemstra, 2005

Canada

Duration of pain: 121 months

RCT

Fair

A. Comprehensive pain management program (n=43):

6 weeks, (18 one-hour sessions 18 hours total) group sessions; outpatient setting

B. Usual care (n=36):

Mean age: 50

% Male: 15%

Race/ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability: NR

Comorbidities (all self-reported):

-

Fatigue: 94%

-

Sleep deprivation: 96%

-

Emotional problems: 64%

-

Headaches: 77%

-

Morning stiffness: 94%

-

Depression: 89%

-

Anxiety: 67%

-

Frustration: 82%

A vs. B, Mean (SD) changes scores from baseline

VAS average pain in last month (0-10)

Baseline (mean, SD): 7.14 (1.37) vs. 7.56 (1.38)

Postintervention change: −1.02 (1.48) vs. −0.22 (1.2), difference in change scores −0.80 (95% CI −1.46 to −0.14)

Number of days in last month with pain

Baseline (mean, SD): 28.86 (3.19) vs. 28.82 (4.45)

Postintervention change: −7.49 (9.35) vs. −1.17 (6.36), difference in change scores −6.32 (95% CI – 10.28 to −2.36)

PDI (0-70)

Baseline (mean, SD): 33.63 (10.78) vs. 33.47 (7.89)

Postintervention change: −8.70 (8.93) vs. −1.97 (9.36), difference in change scores −6.73 (95% CI – 11.07 to −2.38)

A vs. B, Mean (SD) changes scores from baseline

BDI (0-63)

Baseline (mean, SD): 18.23 (10.72) vs. 17.89 (10.03)

Postintervention change: −7.74 (6.92) vs. −0.97 (4.5), difference in change scores −6.77 (95% CI −9.67 to −3.87)

Self-reported health status (0-5)

Baseline (mean, SD): 3.60 (1.03) vs. 3.67 (0.89)

Postintervention change: −0.60 (0.12) vs. 0.03 (0.11), difference in change scores −0.63 (95% CI −0.95 to −0.31)

NR

Linton, 2005

Sweden

Duration of pain: NR (>12 weeks: 84%)

RCT

Fair

A. Comprehensive pain management program (n=69):

6 weeks (1x/week, 2 hours, at least 12 total) group sessions; outpatient setting

B. Usual care (n=47)

Mean age: 48 years

% Male: 16%

Race/ethnicity: NR

Pain etiology/type:

-

Back pain: 90%

-

Neck pain: 10%

Disability: NR

Comorbidities: NR

Mean (SD)

Average pain last week (0-10)

Baseline: 4.4 (2.1) vs. 5.0 (2.3)

Long term (12 months): 2.9 (2.1) vs. 4.1 (2.8), difference −1.20 (95% CI – 2.19 to −0.21)

Average pain last 3 months

Baseline: 4.5 (1.9) vs. 4.7 (1.6)

Long term (12 months): 3.0 (1.8) vs. 4.1 (2.5), difference −1.10 (95% CI −1.94to −0.26)

Worst pain last 3 months

Baseline: 6.0 (2.3) vs. 6.2 (2.1) 12 months: 4.3 (2.8) vs. 5.4 (2.8), difference −1.10 (95% CI −2.21 to 0.01)

Pain-free days in last week (0-7)

Baseline: 2.3 (2.5) vs. 2.2 (2.5)

Long term (12 months): 3.5 (3.0) vs. 2.8 (2.7), difference 0.70 (95% CI – 0.44 to 1.84)

Modified RMDQ (0-18)

Baseline: 3.7 (4.5) vs. 3.3 (3.7)

Long term (12 months): 3.4 (4.2) vs. 4.0 (4.7), difference −0.60 (95% CI – 2.34 to 1.14)

Activities of Daily Living (0-50)

Baseline: 38.9 (10.6) vs. 40.0 (8.2)

Long term (12 months): 41.5 (10.4) vs. 41.1 (8.9), difference 0.40 (95% CI −3.48 to 4.28)

Mean (SD)

HADS Anxiety (0-21)

Baseline: 4.9 (3.8) vs. 6.1 (4.2)

Long term (12 months): 5.2 (3.6) vs. 7.1 (4.9), difference −1.9 (95% CI −3.55 to – 0.25)

HADS Depression (0-21)

Baseline: 3.8 (3.4) vs. 4.3 (3.7)

Long term (12 months): 3.8 (3.6) vs. 4.5 (4.4), difference −0.70 (95% CI −2.26 to 0.86)

NR

Peters 1990, 1992

New Zealand

Duration of pain: 6 to 48 months,49%; 48 months to 240+ months, 51%

RCT

Poor

A. Comprehensive pain management program, Inpatient group (n=23): 5 days a week for 4 weeks, (hours total unclear)

group sessions; inpatient (Monday – Friday)

B. Comprehensive pain management program, Outpatient group (n=29) 9 weeks, (one 2-hour session per week, 18 hours total)

group sessions; outpatient

C. Usual care (n=16)

Mean age: 44 years

% Male: 38%

Race/Ethnicity:

-

European: 93%

-

Maori: 4%

-

Polynesian: 3%

Pain etiology/type Mixed chronic pain (patient could have more than one pain type):
-

Back pain: 43%

-

Head pain: 35%

-

Arm pain: 26%

-

Leg pain: 18%

-

Chest pain: 10%

-

Abdomen pain: 6%

Disability: NR

Comorbidities: NR

A vs. B vs. C, Mean (SD)

VAS pain (0-10)

A vs. C

Baseline: 5.12 (2.56) vs. 4.21 (2.55)

Postintervention: 3.92 (2.33) vs. 5.29 (2.70)

B vs. C

Baseline: 5.25 (2.46) vs. 4.21 (2.55)

Postintervention: 4.25 (2.18) vs. 5.29 (2.70)

SIP (0-100)

A vs. C

Baseline: 204.31 (75.43) vs. 165.00 (125.26)

Postintervention: 122.89 (80.84) vs. 180.67 (152.40)

Long-term followup: NR

B vs. C

Baseline: 137.78 (105.49) vs. 165.00 (125.26)

Postintervention: 96.00 (78.84) vs. 180.67 (152.40)

A vs. B vs. C, % (n/N)

Proportion of patients taking an opioid

Baseline:

Any opioid: 31.8% (7/22) vs. 33% (6/18) vs. 50% (6/12)

-

strong opioid: 9.1% (2/22) vs. 17% (3/18) vs. 0% (0/12)

-

mild opioid: 22.7% (5/22) vs. 17% (3/18) vs. 50% (6/12)

Postintervention: NR

Long-term followup:

Any opioid: 13.6% (3/22) vs. 22% (4/18) vs. 66.7% (8/12)

-

strong opioid: 0% (0/22) vs. 6% (1/18) vs. 8.3% (1/12)

-

mild opioid: 13.6% (3/22) vs. 17% (3/18) vs. 58.3% (7/12)

A vs. B vs. C, Mean (SD)

BDI (0-63)

A vs. C

Baseline: 19.18 (9.34) vs. 12.33 (7.29)

Postintervention: 12.25 (15.64) vs. 11.07 (5.82)

B vs. C

Baseline: 13.55 (6.03) vs. 12.33 (7.29)

Postintervention: 10.73 (6.16) vs. 11.07 (5.82)

GHQ (0-36)

A vs. C

Baseline: 15.52 (8.58) vs. 11.50 (10.08)

Postintervention: 5.96 (7.11) vs. 10.36 (9.46)

B vs. C

Baseline: 8.67 (7.23) vs. 11.50 (10.08)

Postintervention: 5.91 (6.42) vs. 10.36 (9.46)

A vs. B vs. C, % (n/N)

Proportion of patients reported to be “nonactive” (i.e., those receiving accident compensation, unemployment benefit, sickness benefit, invalids benefit, health insurance, or unable to manage a home) % (n/N)

Baseline: 82% (18/22) vs. 67% (13/18) vs. 33% (4/12)

Postintervention: NR

Long-term followup: 18% (4/22) vs. 33% (6/18) vs. 58% (7/12)

Proportion of patients demonstrating treatment “success” (using medication appropriately + active + no pain increase), % (n/N)

Postintervention: NR

Long-term followup: 68% (15/22) vs. 61% (11/18) vs. 25% (3/12)

NR

Saral, 2016

Turkey

Duration of pain: 90 months

RCT

Fair

A. Comprehensive pain management program, long-term group (n=22): 10 weeks (~7.5 hours/week; ~75 hours total); group + individual sessions; outpatient

B. Comprehensive pain management program, short-term group (n=22): 2 days (~10 hours total); group + individual sessions; outpatient

C. Usual care (n=22)

Mean age: 42 years

% Male: 0% (female only for inclusion)

Race/ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability: NR

Comorbidities: NR Other characteristics:

-

Excluded: history of severe trauma, advanced psychiatric diseases, serious physical comorbidities

A vs. B vs. C, Mean (SD)

VAS pain (0-10)

Baseline: 8.2 (0.9) vs. 7.6 (0.8) vs. 7.5 (0.9)

Intermediate term: 5.1 (2.4) vs. 5.8 (1.0) vs. 7.6 (1.4)

FIQ (0-100)

Baseline: 71.6 (14.2) vs. 67.7 (12.0) vs. 65.5 (13.2)

Intermediate term: 53.9 (19.3) vs. 54.5 (14.2) vs. 65.5 (11.5)

A vs. B vs. C, Mean (SD)

BDI (0-63)

Baseline: 23.4 (11.0) vs. 20.7 (6.6) vs. 21.4 (10.4)

Intermediate term:16.6 (9.6) vs. 15.0 (10.2) vs. 18.7 (9.5)

SF-36 PCS (0-100)

Baseline: 32.8 (7.9) vs. 36.5 (8.7) vs. 36.0 (7.2)

Intermediate term: 39.9 (7.5) vs. 39.6 (8.1) vs. 34.3 (8.1)

SF-36 MCS (0-100)

Baseline: 30.4 (11.7) vs. 33.2 (8.9) vs. 36.1 (9.8)

Intermediate term: 40.7 (12.3) vs. 40.2 (10.0) vs. 37.6 (10.0)

NR

Scholten, 1999

Austria

Duration of pain: 106.8 months

RCT

Poor

A. Comprehensive pain management program (n=38):

9 days over 2 weeks, (unclear hours total)

group; outpatient setting

B. Waitlist control (n=30):

Mean age: 48 years

% Male: 21%

Race/ethnicity: NR

Pain etiology/type: Rheumatoid arthritis Joint status (Steinbrocker’s criteria):

-

functional class I: 21%

-

functional class II: 54%

-

functional class III: 25%

Disability: NR

Comorbidities: NR

A vs. B, mean (SD)

Stanford Health Assessment Questionnaire (1-5)

Baseline: 2.6 (0.78) vs. 2.9 (0.62)

Postintervention: 1.6 (0.41) vs. 2.9 (0.68)

Short term: 1.8 (0.54) vs. 2.7 (0.71)

Intermediate term: 2.2 (0.32) vs. 2.6 (0.69)

A vs. B, mean (SD)

BDI (0-63)

Baseline: 12.1 (6.2) vs. 12.0 (6.4)

Postintervention: 6.9 (3.6) vs. 12.2 (6.5)

Short term: 8.2 (3.0) vs. 11.9 (7.0)

Intermediate term: 9.6 (2.3) vs. 12.1 (6.5)

FQCI, Depression (5-25)

Baseline: 12.7 (6.6) vs. 11.9 (5.3)

Postintervention: 10.7 (4.2) vs. 12.4 (5.9)

Short term; 10.0 (3.7) vs. 12.3 (5.9)

Intermediate term: 10.8 (2.0) vs. 12.7 (6.2)

NR

Smeets, 2006a, 2008

Netherlands

Duration of pain: 56.7 months

Cluster RCT

Fair

A. Comprehensive pain management program (n=61):

3 days a week for 10 weeks, (1.75 hours/day, 3 times a week 52.5 hours total)

Group and individual sessions; outpatient setting

B. Waitlist control (n=51):

Mean age: 42 years

% Male: 53%

Race/ethnicity: NR

Mean duration of functional limitations: 35.1 months

Pain etiology/type: Chronic LBP

-

radiation of pain below knee: 49%

-

radiation of pain above knee: 37%

-

without radiation of pain: 14%

Disability:
-

Full sick leave/disability pension: 38%

-

Partial sick leave/disability pension: 24%

Comorbidities: NR

Other characteristics:

-

Previous back surgery: 15%

-

Trauma preceding LBP:18%

A vs. B, adjusted mean (SD)a

VAS, current pain (0-10)

Baseline: 4.598 (2.395) vs. 5.102 (2.540)

Postintervention: 4.231 (2.556) vs. 5.335 (2.26); adjusted difference −0.823 (95% CI −1.637 to −0.010)a

VAS, main complaints (0-10)

Baseline: 7.244 (1.703) vs. 7.742 (1.135)

Postintervention: 5.468 (2.179) vs. 7.425 (1.47); adjusted difference −1.784 (95% CI −2.654 to −0.914)a

PRI-T (scale NR)

Baseline: 18.08 (9.04) vs. 17.37 (8.52)

Postintervention: 17.53 (10.53) vs. 17.28 (10.48); adjusted difference −0.33 (95% CI −4.14 to 3.48)a

RMDQ (0-24)

Baseline: 13.51 (3.92) vs. 13.96 (3.88)

Postintervention: 11.40 (5.25) vs. 13.88 (4.78); adjusted MD −2.56 (95% CI −4.27 to −0.85)a

A vs. B, adjusted mean (SD)a

BDI (0-63)

Baseline: 9.75 (6.68) vs. 9.78 (7.67)

Postintervention: 9.07 (6.53) vs. 9.42 (7.81); adjusted difference 0.04 (95% CI −1.71 to 1.79)a

Global Improvement (1-7)

Postintervention: 4.53 (1.33) vs. 3.78 (0.91); adjusted difference 0.70 (95% CI 0.17 to 1.24)a

Harms:

Increased pain in the lower back or radiating leg pain: 5.5% (3/55)

Satisfaction (0-100 VAS): 10th percentile of baseline RMDQ (=9):

Postintervention: 64.98 (25.30) vs. 45.65 (25.30); adjusted MD 19.33 (95% CI 2.01 to 36.65)a

50th percentile of baseline RMDQ (=14)

Postintervention: 70.24 (25.30) vs. 46.67 (25.30); adjusted MD 23.57 (95% CI 11.28 to 35.86)a

90th percentile of baseline RMDQ (=19)

Postintervention: 75.50 (25.30) vs. 47.69 (25.30); adjusted MD 27.81 (95% CI 9.54 to 46.08)a

Smith, 2019

Australia

Duration of pain: >60 months, 59% <5 60 months, 41%

RCT

Fair

A. Comprehensive pain management program (n=41):

8 (online lessons with a 2-week gap between each lesson) 16 weeks, (hours total NR)

Individual sessions; outpatient (online)

B. Usual care (n=39):

Mean age: 45 years

% Male: 12.5%

Race: NR

Pain etiology/type: Chronic pain

-

injury-related pain: 51%

-

noninjury related pain: 9%

Disability: NR

Comorbidities: NR

Prescribed medication:

-

opioid: 54%

-

gabanoid: 31%

-

simple analgesia: 69%

-

any: 90%

-

for anxiety/major depressive disorder: 40%

-

major depressive disorder: 24%

A vs. B, estimated marginal mean (SD)

BPI Severity (0-10)

Baseline: 5.40 (1.66) vs. 5.05 (1.66)

Postintervention: 4.44 (1.56) vs. 4.73 (1.63), difference −0.29 (95% CI −1.07 to 0.49)

Short term: 4.38 (1.58) vs. 4.77 (1.64), difference −0.39 (95% CI – 1.18 to 0.40)

BPI Interference (0-10)

Baseline: 6.70 (2.10) vs. 5.88 (2.10)

Postintervention: 4.90 (1.98) vs. 4.82 (2.04)

Short term: 5.19 (1.98) vs. 4.64 (2.05)

PDI (scale 0-70)

Baseline: 38.33 (10.07) vs. 37.06 (10.04)

Postintervention: 26.59 (9.88) vs. 33.64 (9.97)

Short term: 30.47 (9.89) vs. 32.44 (9.94)

A vs. B, % (n/N)

Opioid use

Baseline: 56.1% (23/41) vs. 51.3% (20/39)

Postintervention: 63.3% (19/30) vs. 50.0% (17/34)

Short term: 60.0% (18/30) vs. 51.5% (17/33)

A vs. B, estimated marginal mean (SD)

PHQ-9 (0-27)

Baseline: 11.42 (5.78) vs. 10.55 (5.88)

Postintervention: 9.58 (5.36) vs. 9.51 (5.70)

Short term: 9.81 (5.45) vs. 9.26 (5.65)

Major Depressive Disorder Diagnosis:

Baseline: 34% (12/35) vs. 18% (6/33)

Short term: 17% (6/35) vs. 33% (11/33)

NR

Turner, 1990

USA

Duration of pain:

155 months

RCT

Poor

A. Comprehensive pain management program (n=18): 8 weeks (4 hours/week, 32 hours total); group + individual sessions; outpatient

B. Waitlist control (n=39)

Mean age: 44 years

% Male: 52.1%

Race/ethnicity: White: 100%

Pain etiology/type: Chronic LBP

Disability: NR

Comorbidities: NR

A vs B, Mean (SD)

MPQ (0-78)

Baseline: 25.54 (12.41) vs. 21.17 (8.84)

Postintervention: 14.78 (11.44) vs. 20.95 (10.62) [on a 0-10 scale, 1.9 (1.5) vs. 2.7 (1.4), difference −0.79 (95% CI −1.70 to 0.12)]

SIP (scale NR)

Baseline: 8.50 (4.59) vs. 6.24 (4.99)

Postintervention: 3.63 (2.98) vs. 5.37 (5.93)

A vs. B, Mean (SD)

CES-D (0-60)

Baseline: 12.38 (7.31) vs.10.48 (4.19)

Postintervention: 7.36 (5.89) vs. 7.03 (5.02)

A vs. B, Mean (SD)

Patient satisfaction (1-7)

5.50 (NR) vs. NR

van Eijk-Hustings, 2013, 2016

Netherlands

Duration of pain: 81.6 months

RCT

Fair

A. Comprehensive pain management program (n=108):

12 weeks*, (2x/week, 1.5 hours/day 36 hours total) group sessions outpatient setting

*(+ 9-month aftercare program)

B. Usual care (n=48):

Mean age: 42 years

% Male: 4%

Race/ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability: NR

Comorbidities: NR

A vs. B, Estimated marginal means (SD)

FIQ Total (0-100)

Baseline: 64.5 (14.55) vs. 55.4 (15.93)

Postintervention: 55.1 (15.59) vs. 58.1 (15.93)

Long term (18 months): 50.9 (20.78) vs. 56.2 (20.09); effect size 0.25 (95% CI −0.09 to 0.59)

A vs. B, Estimated marginal means (SD)

EQ-5D scale?

Baseline: 0.36 (0.31) vs. 0.51 (0.28)

Postintervention: 0.49 (0.31) vs. 0.50 (0.28)

Long term (18 months): 0.55 (0.31) vs. 0.51 (0.35); effect size 0.12 (95% CI −0.22 to 0.46)

EQ5D VAS, overall impression of health (0-100)

Baseline: 48.1 (17.67) vs. 54.0 (18.01)

Postintervention: 54.0 (19.75) vs. 48.3 (20.09)

Long term (18 months): 57.3 (23.90) vs. 51.9 (22.89); effect size 0.22 (95% CI – 0.12 to 0.56)

FIQ, Depression (0-10)

Baseline: 5.2 (3.12) vs. 4.2 (2.77)

Postintervention: 4.1 (3.12) vs. 4.5 (2.77)

Long term (18 months): 3.9 (3.12) vs 4.2 (2.77); A vs. B, effect size 0.10 (95% CI – 0.24 to 0.44)

FIQ, Anxiety (0-10)

Baseline: 5.9 (3.12) vs. 4.8 (2.77)

Postintervention: 5.0 (2.08) vs. 5.2 (2.77)

Long term (18 months): 4.7 (3.12) vs. 4.8 (2.77); A vs. B, effect size 0.03 (95% CI – 0.31 to 0.37)

A vs. B, Estimated marginal means (SD)

Average resource use per patient per 2 months, mean (IQR) or % (n/N):

Formal home help:

Baseline: 0.2 (0 to 0) vs. 0.1 (0 to 0)

During intervention: 0.4 (0 to 0) vs. 0.6 (0 to 0)

Postintervention: 0.4 (0 to 0) vs. 0.5 (0 to 0)

Paid home help:

Baseline: 0.1 (0 to 0) vs. 0.2 (0 to 0)

During intervention: 0 (0 to 0) vs. 0.1 (0 to 0)

Postintervention: 0.3 (0 to 0.5) vs. 0.1 (0 to 0.2)

Informal care:

Baseline: 0.6 (0 to 0) vs. 0.3 (0 to 0)

During intervention: 1.6 (0 to 1.5) vs. 0.6 (0 to 0.4)

Postintervention: 0.9 (0 to 1.1) vs. 0.6 (0 to 0.8)

van Koulil, 2010, 2011

Netherlands

Duration of pain: NR

Cluster RCT

Fair

A. Comprehensive pain management program, pain avoidance treatment tailoring group (n = 29): 8 weeks (32 hours) + booster session (4 hours) 3 months after treatment conclusion (36 hours total); individual sessions; outpatient

B. Comprehensive pain management program, pain persistence treatment tailoring group (n = 39): 8 weeks (32 hours) + booster session (4 hours) 3 months after treatment conclusion (36 hours total); individual sessions; outpatient

C. Waitlist control, pain avoidance treatment (n = 45)

D. Waitlist control, pain persistence treatment (n = 45)

Mean age: 42 years

Male: 6%

Race/ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability: NR

Comorbidities:

-

self-reported heightened psychological distress (part of inclusion criteria)

A vs. B vs. C vs. D, Mean (SD)

IRGL pain (6-25)

Baseline: 20.3 (2.4) vs. 19.1 (3.7) vs. 19.8 (3.1) vs. 17.6 (3.4)

Postintervention: 16.0 (3.2) vs. 15.9 (3.8) vs. 20.0 (4.3) vs. 17.4 (3.5)

Short term: 17.2 (3.3) vs. 16.4 (5.1) vs. 20.4 (3.4) vs. 16.4 (3.6)

FIQ (0 to 100)

Baseline: 66.3 (11.6) vs. 57.2 (11.0) vs. 67.0 (11.8) vs. 54.1 (14.7)

Postintervention: 47.6 (14.7) vs. 46.8 (15.3) vs. 63.6 (14.9) vs. 53.9 (12.8)

Short term: 50.0 (15.6) vs. 43.2 (18.5) vs. 66.0 (13.9) vs. 50.8 (15.2)

IRGL mobility (7-28)

Baseline: 13.6 (3.0) vs. 18.6 (4.5) vs. 13.6 (3.0) vs. 18.7 (4.3)

Postintervention: 18.4 (3.5) vs. 21.4 (4.0) vs. 14.5 (4.3) vs. 19.4 (4.1)

Short term: 19.3 (3.8) vs. 22.2 (4.8) vs. 14.5 (4.2) vs. 19.8 (4.4)

A vs. B vs. C vs. D, Mean (SD)

IRGL negative mood scale (0-24)

Baseline: 8.9 (3.8) vs. 5.9 (3.3) vs. 10.5 (5.7) vs. 5.6 (3.6)

Postintervention: 4.7 (3.7) vs. 4.0 (3.5) vs. 8.8 (6.2) vs. 6.3 (3.7)

Short term: 5.0 (3.5) vs. 3.5 (2.6) vs. 8.4 (5.2) vs. 6.1 (4.5)

IRGL anxiety scale (10-40)

Baseline: 26.3 (5.9) vs. 23.2 (4.3) vs. 27.0 (6.4) vs. 23.9 (5.1)

Postintervention: 21.6 (5.9) vs. 20.6 (4.3) vs. 25.6 (6.7) vs. 23.6 (5.2)

Short term: 20.3 (5.6) vs. 19.0 (4.4) vs. 26.0 (5.4) vs. 22.7 (5.4)

NR

Weiner 2020

USA

Duration of pain: 3 months

RCT

Fair

A. Comprehensive pain management program (n=25):

duration NR, (6 months total)

Individual or group sessions NR; outpatient setting

B. Usual care (n=30): Standard clinical care

Mean age: 69 years

% Male: 96%

Race:

-

Black: 31%

-

White: 67%

-

Unknown: 2%

Ethnicity:
-

Not Hispanic: 93%

Pain etiology/type: Chronic LBP

Disability:

-

due to LBP: 15%

-

due to Other: 5%

Comorbidities:
-

General: 69%

-

Diabetes: 29%

-

Lung: 29%

-

Cardiovascular: 27%

-

Cancer: 18%

-

Neurological: 11%

Mean Duke comorbidity index: 3.5

Current Medications:

-

NSAID: 40%

-

Opioid: 27%

-

Gabapentin: 20%

-

Skeletal muscle relaxant: 13%

-

Acetaminophen: 13%

-

Topical: 5%

-

Antidepressant: 4%

-

Other: 4%

-

Salicylate: 2%

-

Corticosteroid, pregabalin: 0%

A vs. B, Mean (SD) change scores from baseline to followup

VAS pain, Current (0-10)

Baseline: mean 4.5 (2.8) vs. mean 5.3 (2.4)

Postintervention: 0.46 (2.99) vs.0.96 (2.18); unadjusted difference in change scores −0.46 (SE 0.72), p=0.53; adjustedb difference in change scores −1.07 (SE 0.59), p=0.07

VAS pain, Average over prior week (0-100)

Baseline: mean 6.6 (1.7) vs. mean 6.5 (1.4)

Postintervention: −1.38 (2.46) vs. – 0.08 (2.02); unadjusted difference in change scores −1.24 (SE 0.62), p=0.046; adjustedb MD in change scores −1.22 (SE 0.54), p=0.02

VAS pain, Worst pain over prior week (0-10)

Baseline: mean 8.8 (1.5) vs. mean 8.5 (1.9)

Postintervention: −2.25 (2.44) vs. – 0.42 (1.42); unadjusted difference in change scores −1.74 (SE 0.60), p=0.004; adjustedb difference in change scores −1.70 (SE 0.57), p=0.003

RMDQ (0-24)

Baseline: mean 14.8 (5.1) vs. 15.1 (5.3)

Postintervention −1.29 (6.05) vs. 0.08 (4.12); unadjusted difference in change scores −1.24 (SE 1.28), p=0.33; adjustedb difference in change scores −1.42 (SE 1.25), p=0.26

A vs. B, Mean (SD) change scores from baseline to followup

SF-12 PCS (0-100)

Baseline: mean 31.2 (8.1) vs. mean 32.5 (9.4)

Postintervention: 1.46 (8.38) vs. −1.08 (8.84); unadjusted difference in change scores 2.36 (SE 2.23), p=0.29; adjustedb difference in change scores 2.17 (SE 2.12), p=0.31

SF-12 MCS (0-100)

Baseline: mean 51.7 (11.4) vs. mean 51.3 (10.8)

Postintervention: −1.14 (9.55) vs. −3.12 (10.59); unadjusted MD in change scores 2.12 (SE 2.60), p=0.42; adjustedb difference in change scores 2.47 (SE 2.46), p=0.32

NR

Whitfill, 2010

USA

Duration of pain:

NR

RCT

Poor

A. Comprehensive pain management program (n=90): 4 to 10 weeks; intensity unclear; individual sessions; outpatient

B. Usual care (n=52)

Mean age: 40 years

% Male: 50%

Race/ethnicity:

-

Caucasian: 51.7% vs. 40.3%

-

Latino: 19.0% vs. 20.7%

-

African American: 27.6% vs. 32.0%

-

Asian: 1.7% vs. 7.0%

-

Other: 0.0% vs. 0.0%

Pain etiology/type: Low back pain

Disability: NR

Other characteristics: NR

A vs. B, Mean (SD)

VAS pain (0-10)

Baseline: 6.00 (2.07) vs. 5.95 (1.95)

Intermediate term: 3.91 (2.86) vs. 5.07 (2.78), difference −1.16 (95% CI −2.26 to −0.06)

CPI (0-10)

Baseline: 5.23 (2.51) vs. 2.50 (2.45)

Intermediate term: 2.96 (2.82) vs. 4.27 (3.01)

A vs. B, Mean (SD)

SF-36 (0 to 100)

Baseline: 33.00 (8.09) vs. 35.99 (10.13)

Intermediate term: 40.47 (11.47) vs. 39.45 (10.59)

BDI (0 to 63)

Baseline: 11.63 (9.30) vs. 9.43 (9.58)

Intermediate term: 8.81 (9.49) vs. 10.11 (10.23)

NR

Williams, 1996 UK

Duration of pain: 93.7 months

RCT

Poor

A. Comprehensive pain management program, inpatient group (n=43): 4.5 days a week for 4 weeks, (28 hours total) group sessions; inpatient

B. Comprehensive pain management program, outpatient group (n=45): 8 weeks, (3.5 hours a week, 28 hours total) group sessions outpatient

C. Waitlist control (n=33)

Mean age: 50 years

% Male: 47%

Race/ethnicity:

Afro-Caribbean or Asian: 12%-16%

White: 84%-88%

Pain etiology/type: Mixed chronic pain

-

back/neck/legs: 74%

-

≥1 surgery: 39%

-

central/peripheral nerve system damage: 26%

-

other tissue damage: 16%

-

unknown mechanism: 58%

Receiving disability income: 62%

Litigation related to pain: 21%

Opioid use: 61%

Excess drug use: 59%

A vs. B vs. C, mean (SD)

VAS pain intensity (0-10)

Baseline: 7.11 (1.90) vs. 6.86 (1.49) vs. 6.79 (2.23)

Short term: 6.10 (2.17) vs. 6.34 (1.96) vs. 6.81 (2.07); p=NS

VAS pain distress (0-10)

Baseline: 6.64 (2.24) vs. 7.03 (2.10) vs. 6.05 (2.31)

Short term: 4.16 (2.90) vs. 5.42 (2.75) vs. 6.30 (2.53); p=NS

SIP (0-100)

Baseline: 29.53 (12.55) vs. 28.48 (9.49) vs. 28.44 (9.83)

Short term: 15.81 (11.20) vs. 20.95 (10.29) vs. 29.65 (10.82); p<0.0005

A vs. B vs. C

Opioid use: no use of opioids

Baseline: 47% (18/38) vs. 33% (11/33) vs. NR

Short term: 82% (31/38) vs. 57% (19/33) vs. NR

Long term (12 months): 80% (24/38) vs. 55% (17/33) vs. NR

Opioid dose equivalent to >10 mg morphine per day:

Baseline: 34.2% (13/38) (mean 30 mg, maximum of 120 mg/day) vs. 48.5% (16/33) (mean 22 mg, maximum of 60 mg/day) vs. NR

Short term: 10.5% (4/38) (maximum of 30 mg/day) vs. 33.3% (11/33) (maximum of 45 mg/day) vs. 32.3% (10/31), p=NS

Long term (12 months): 10.5% (4/38) (mean 22 mg, maximum of 45 mg/day) vs. 18.2% (6/33) (mean 15 mg, maximum of 70 mg/day) vs. NR, p=NS

A vs. B vs. C, mean (SD)

BDI (0-63)

Baseline: 17.8 (8.0) vs. 16.8 (5.6) vs. 16.6 (6.5)

Short term: 9.5 (7.8) vs. 12.2 (6.3) vs. 17.3 (7.0); p<0.0005

STAI (20-80)

Baseline: 45.1 (10.7) vs. 45.7 (8.2) vs. 44.8 (11.6)

Short term: 36.8 (13.6) vs. 42.3 (10.6) vs. 45.0 (11.7), p<0.05 for all

A vs. B vs. C

Utilization:

Subsequent treatments:

-

Surgery: 0% for all groups

-

Any, to include the above as well as prescribed and nonprescribed analgesics: 44.8% (13/29) vs. 85.7% vs. NR (24/28); RR 0.52 (95% CI 0.34 to 0.80)

ADL = activities of daily living;; BDI = Beck Depression Inventory; BPI = Brief Pain Inventory; CES-D = Center for Epidemiological Studies Depression Scale; CIS = Checklist Individual Strength; CPI = Characteristic Pain Inventory; EQ-5D = Five-dimensional EuroQol; FIM = Functional independence measure, FIQ = Fibromyalgia Impact Questionnaire; FQCI = Freiburg Questionnaire of Coping with Illness; GDS = General Depression Scale; GHQ = General Health Questionnaire; HADS = Hospital Anxiety and Depression Scale Anxiety; HAQ = Health Assessment Questionnaire; HRQOL = health-related quality of life; IRGL = Impact of Rheumatic Diseases on General Health and Lifestyle Instrument; IRQ = interquartile range; MPI = Multidimensional pain inventory; MPQ = The McGill Pain Questionnaire; NR = not reported; NRS = Numeric Pain Rating Scale; NS = not significant; PDI = Pain Disability Index; PHQ-9 = Patient Health Questionnaire–9; PRI-T = Pain Rating Index Total score; RA= Rheumatoid arthritis; RMDQ = Roland and Morris Disability Questionnaire; RCT = randomized controlled trial; SD = standard deviation; SE = standard error; SF-36 = Short-Form 36 questionnaire; SIP = Sickness Impact Profile; STAI = Spielberger State-Trait Anxiety Inventory; VAS = visual analog scale.

a

Estimated adjusting for age, gender, center of treatment, baseline score of outcome measure, duration of functional limitations, and work status, based on a longitudinal random coefficient analysis with an extra random intercept for clusters of four patients being randomized together.

b

Adjusted for baseline scores.

Table B-6Summary results for trials addressing KQ1: CPMPs versus physical activity

Author, Year

Country

Pain Duration

Study Design

Study Quality

Intervention (n)

Comparator (n)

Duration/Intensity

Session Format

Setting (IP/OP)

Population

Primary Outcomes:

Pain, Function, and Opioid Use

Secondary Outcomes: HRQOL, Psychological Measures, Global ImprovementHarms, Utilization, Patient Satisfaction

Alaranta, 1994

Finland

Mean duration of pain: NR (≥6 months)

RCT

Fair

A. CPMP (n=152)

6 weeks, 52 hours total; group + individual; 3 weeks at home + 3 weeks inpatient

B. PA (n=141)

3 weeks 45-60 hours total, session format NR, inpatient

Mean age: 40 years

Male: 45%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

Disability:

-

Million index (0-100): 58.1

Comorbidities:
-

NR

A vs. B, Mean (SD)

MVAS disability (0-100)

(f/u data estimated by EPC from Fig 4 of study publication)

Baseline: 45.5 (18.8) vs. 45.1 (20.8)

Short term: 28.5 (20.9) vs. 35.8 (20.3), difference −7.3 (95% CI −12.1 to 2.5)

Intermediate term: 29.6 (23.2) vs. 36.1 (23.9), difference −6.5 (95% CI −12.0 to – 1.0)

Symptom Check List Pain and Anxiety Subscales: Data not reported (p>0.05)

BDI: Data not reported.

A vs. B

Harms: NR

Decrease (%) in the number of yearly visits

Physician: 74% vs. 67%

Outpatient PT: 69% vs. 77%

Bendix, 1995, 1997, 1998a, 1998b (PROJECT B)

Denmark

Mean duration of pain: NR (≥6 months)

RCT

Fair

A. CPMP, high intensity (n=46)

3 weeks (39 hours/week + one 6hour session /week for 3 weeks, group, outpatient

B. CPMP, lower intensity (n=43)

Twice weekly for 6 weeks (total 24 hours), group, outpatient

C. PA (n=43)

Twice weekly for 6 weeks (total 24 hours), group, outpatient

Mean age: 42 years

Male: 25%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

Disability:

Patient’s perception of disability due to back pain (0-30): 15

Comorbidities:

Smoker: 66%

Prior back surgery: 21%

Disability Index (from LBP Rating Scale, 0-30)

Baseline: 15.5 (NR) vs. 15.3 (NR) vs. 14.4 (NR)

Short term: 8.5 (5 to 15) vs. 16.1 (11 to 19) vs. 13.5 (10 to 17), p=0.002 for A vs. B and A vs. C

Long term (12 months): 8.9 (5 to 13) vs. 16.4 (14 to 19) vs. 13.7 (9 to 17), p<0.001 for A vs. B and A vs. C

Long term (24 months): 10 (6 to 14) vs. 17 (9 to 21) vs. 14 (9 to 17), p=0.002 for A vs. B, p=0.02 for A vs. C

Long term (60 months): 8 (NR) vs. 16 (NR) vs. 14 (NR), p=0.03 for A vs. B, p=0.01 for A vs. C

A vs. B vs. C, Median (IQR)

Back pain VAS (0-10)

Baseline: 5.3 (NR) vs. 5.9 (NR) vs. 5.4 (NR)

Short term: 2.7 (1.4 to 4.3) vs. 5.6 (3.8 to 7.6) vs. 4.4 (2.4 to 6.2), p<0.001 for A vs. B and A vs. C

Long term (12 months): 3.3 (2.1 to 5.6) vs. 6.5 (4.8 to 7.7) vs. 5.3 (3.3 to 7.6), p=0.005 for A vs. B and A vs. C

Long term (24 months): 3 (2 to 6) vs. 6 (4 to 8) vs. 5 (3 to 7), p=0.003 for A vs. B, p=0.07 for A vs. C

Long term (60 months): 4 (NR) vs. 6 (NR) vs. 5 (NR), p=0.3

Leg pain VAS (0-10)

Baseline: 2.9 (NR) vs. 3.7 (NR) vs. 3.7 (NR)

Short term: 0.4 (0 to 2.3) vs. 3.1 (0.5 to 5.9) vs. 2.6 (0.1 to 4.6), p=0.01 for A vs. B and A vs. C

Long term (12 months): 2.1 (0.2 to 4.13) vs. 4.8 (2.3 to 7.3) vs. 2.8 (1.4 to 7.0), p=0.001 for A vs. B, p=0.04 for A vs. C

Long term (24 months): 2 (0 to 5) vs. 5 (1 to 6) vs. 4 (2 to 6), p=0.08

Long term (60 months): 3 (NR) vs. 4 (NR) vs. 4 (NR), p=0.07

NR

A vs. B vs. C, Median (IQR)

Harms: NR

Number contacts to any health-care professional

Short term: 0.5 (0 to 2.4) vs. 2.8 (0.4 to 4.6) vs. 1.3 (0.1 to 3.1), p=NS for A vs. B, p<0.05 for A vs. C

Long term (12 months): 4.5 (0.3 to 12.3) vs. 12.0 (0.8 to 23.3) vs. 11.8 (4.0 to 25.0), p=0.002 for A vs. B and A vs. C

Long term (24 months): 5 (0 to 19) vs. 21 (3 to 34) vs. 14 (7 to 27), p=0.03

Long term (60 months): 15 (NR) vs. 10 (NR) vs. 24 (NR), p=0.20

Proportion of patients hospitalized due to LBP, % (n/N)

Long term (60 months): 22% (8/37) vs. 23% (7/31) vs. 24% (7/29), p=1.0

Proportion who underwent back surgery during study period, % (n/N)

Long term (60 months): 5% (2/37) vs. 10% (3/31) vs. 10% (3/29), p=0.70

Bendix, 2000

Denmark

Mean duration of pain: NR (≥6 months)

RCT

Fair

A. CPMP (n=59)

3 weeks (40 hours/week), then 1 day weekly for 3 weeks + a 6-hour follow-up, group, outpatient

B. PA (n=68)

8 weeks (1.5 hour per day, 3x/week, 36 hours total), group, outpatient

Median age: 41 years

Male: 35%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

Disability:

-

Working capable: 46%

Comorbidities: NR

A vs. B, Median (IQR)

Back pain VAS (0-10)

Baseline: 5.1 (4 to 7) vs. 6.0 (5 to 7)

Long term: 5.1 (2 to 7) vs. 5.7 (3 to 7.3)

Leg pain VAS (0-10)

Baseline: 2.2 (0 to 5) vs. 3.2 (0 to 6)

Long term: 2.8 (0 to 7) vs. 3.5 (1 to 6.3) (ns)

Disability Index (from LBP Rating Scale, 0-30)

Baseline: 16 (12 to 20) vs. 16 (12 to 21)

Long term: 12 (6 to 21) vs. 13 (9 to 19)

A vs. B, Median (IQR)

Overall assessment of how much the treatment influenced the QoL (0-5)

Long term: 1.7 (1 to 3) vs. 2.7 (2 to 3.3) (P=0.03)

A vs. B, Median (IQR)

Harms: NR

Number contacts to any health-care professional

Long term: 2.5 (0 to 10) vs. 4 (0 to 12.3) (ns)

Henchoz, 2010

Switzerland

Mean duration of pain: NR (>6 weeks)

RCT

Fair

A. CPMP (n=40)

3 weeks (~31 hours/week, 93 hours total), group + individual, outpatient

B. PA (n=27)

9 weeks (1.5 hours/week, 13.5 hours total), individual, outpatient

Mean age: 40 years

Male: 67%

Race/Ethnicity: NR

Pain etiology/type: LBP

Disability: NR

Comorbidities: NR

A vs. B, Mean (SD)

ODI (0-100)

Baseline: 37.6 (15.8) vs. 39.1 (14.7)

Postintervention: 30.1 (16.5) vs. 37.2 (13.5), difference −7.1 (95% CI −14.75 to 0.55)

Short term: 25.7 (15.8) vs. 35.0 (12.3), difference −9.3 (95% CI −16.51 to −2.09)

Intermediate term (6 months): 28.6 (18.4) vs. 35.4 (15.0), difference −6.8, (95% CI – 15.32 to 1.72)

Intermediate term (9 months): 29.6 (17.9) vs. 39.8 (17.3), difference −10.2, (95% CI −18.99 to −1.41)

Long term (12 months): 26.2 (18.0) vs. 38.0 (18.4), difference −11.8 (95% CI – 20.83 to −2.77)

NRNR

Jensen, 2001

Sweden

Mean duration of pain: 31 months

RCT

Fair

A. CPMP (n=63)

4 weeks (20 hours/week, 80 hours total, plus six 90-minute booster sessions over 1 year after treatment), group, outpatient

B. PA (n=54)

Duration: 4 weeks (20 hours/week, 80 hours total, plus six 90-minute booster sessions over 1 year after treatment), group + individual, outpatient

Mean age: 43 years

% Male: 45%

Race/Ethnicity:

-

Swedish origin: 67%

Pain etiology/type: Chronic nonspecific spinal pain
-

Cervical/thoracic pain: 42%

-

Lumbar pain: 46%

-

Mixed pain areas: 12%

Disability: NR
-

Mean total sick leave in 6 months prior to inclusion in study: 292 (63)

Comorbidities: NR

NR

A vs. B, Mean (SD)

SF-36 Global health (0-100)

Females only

A vs. B (n=30 vs. 37)

Baseline: 38.1 (14.5) vs. 35.1 (11.4)

Postintervention: 47.6 (18.0) vs. 41.0 (15.1), difference 6.6 (95% CI −1.48 to 14.68)

Intermediate term: 52.4 (21.6) vs. 43.6 (22.7), difference 8.8 (95% CI −2.10 to 19.70)

Long term: 53.1 (24.5) vs. 47.2 (24.7), difference 5.9 (95% CI −6.18 to 17.98)

Males only

A vs. B (n=33 vs. 17)

Baseline: 41.6 (14.6) vs. 42.6 (13.3)

p=ns

Postintervention: 48.5 (17.2) vs. 46.3 (14.4), difference 2.2 (95% CI −7.60 to 12.00)

Intermediate term: 54.3 (18.3) vs. 50.3 (16.5), difference 4.0 (95% CI −6.64 to 14.64)

Long term: 57.2 (21.8) vs. 52.4 (17.9), difference 4.8 (95% CI −7.56 to 17.16)

A vs. B, Mean (SD)

Harms: NR

Perceived treatment appropriateness (0-10)

Females only

A vs. B (n=30 vs. 37)

Postintervention: 6.4 (3.1) vs. 7.1 (3.4), difference −0.70 (95% CI −2.30 to 0.90)

Males only

A vs. B (n=33 vs. 17)

Postintervention: 6.0 (3.6) vs. 6.3 (3.2), difference −0.30 (95% CI −2.38 to 1.78)

Recommend treatment to relative with a similar pain (0-10)

Females only

A vs. B (n=30 vs. 37)

Postintervention: 7.0 (3.7) vs. 7.9 (3.2), difference −0.90 (95% CI −2.58 to 0.78)

Males only

A vs. B (n=33 vs. 17)

Postintervention: 6.1 (4.3) vs. 7.6 (3.8), difference −1.50 (95% CI −3.99 to 0.99)

Jousett, 2004

France

Mean duration of pain: NR

RCT

Fair

A. CPMP (n=43)

5 weeks (6 hours per day, 30 hours total), group + individual, outpatient

B. PA (n=41)

5 weeks (3 hours per week in clinic, 2 hours per week at home, 25 hours total), individual, outpatient

Mean age: 41 years

% Male: 67%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

Disability:

-

On sick leave

-

Mean sick leave days in the 2 prior years: 198 days

Comorbidities:
-

Prior surgery: 25%

-

Prior depression: 30%

-

Smoking: 39%

A vs. B, Mean (SD)

VAS pain (0-10)

Baseline: 5.0 (2.2) vs. 4.6 (2.2)

Intermediate term: 3.1 (2.5) vs. 4.0 (2.8), difference −0.90 (95% CI −2.04 to 0.24)

Dallas Pain questionnaire ADLs subscale (0-100)

Baseline: 53.7 (16.7) vs. 50.3 (16.7)

Intermediate term: 36.7 (23.0) vs. 41.5 (24.4), difference −4.80 (95% CI −15.15 to 5.55)

Quebec Back Pain Disability scale (0-100)

Baseline: 34.6 (15.4) vs. 31.6 (15.9)

Intermediate term: 22.0 (16.0) vs. 22.9 (17.7), difference −0.90 (95% CI −8.27 to 6.47)

A vs. B, Mean (SD)

HADS (0-21):

Baseline: 17.0 (6.5) vs. 14.3 (6.2)

Intermediate term: 12.7 (7.2) vs. 13.4 (6.4), difference −0.70 (95% CI −3.68 to 2.28)

Dallas Pain Questionnaire anxiety/depression subscale (0-100):

Baseline: 40.6 (25.3) vs. 31.8 (23.1)

Intermediate term: 21.6 (22.9) vs. 27.8 (22.2), difference −6.20 (95% CI −16.05 to 3.65)

A vs. B, % (n/N) or Mean (SD)

Harms: NR

Proportion seeking pain treatments

Baseline: 85.7% (63/42) vs. 78.0% (32/41)

Intermediate term: 64.3% (27/42) vs. 61.0% (25/41), RR 1.05 (95% CI 0.76 to 1.47)

Treatment appreciation (1-5)

Intermediate term: 1.9 (0.8) vs. 2.3 (0.9), difference −0.40 (95% CI −0.77 to −0.03)

Kaapa, 2006

Finland

Mean duration of pain: 26 months

RCT

Fair

A. CPMP (n=59)

8 weeks (70 hours total), group + individual, outpatient

B. PA (n=61)

6-8 weeks (10 hours total), individual, outpatient

Mean age: 46

% Male: 0%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

Disability: NR

Comorbidities:

-

Smoker: 31%

A vs. B, Mean (SD)

Low back pain NRS (0-10)

Baseline: 4.6 (1.9) vs. 5.0 (2.6)

Postintervention: 3.3 (2.5) vs. 3.4 (2.4), difference −0.10 (95% CI −0.98 to 0.78)

Intermediate term: 3.3 (2.5) vs. 3.4 (2.5), difference −0.10 (95% CI −1.01 to 0.81)

Long term (12 months): 3.6 (2.7) vs. 3.4 (2.5), difference −0.20 (95% CI −0.80 to 1.20)

Long term (24 months): 3.5 (2.6) vs. 4.0 (2.9), difference −0.50 (95% CI −1.61 to 0.61)

Sciatic pain NRS (0-10)

Baseline: 2.7 (2.7) vs. 3.1 (3.1)

Postintervention: 2.2 (2.7) vs. 2.0 (2.6), difference 0.20 (95% CI −0.76 to 1.16)

Intermediate term: 2.3 (2.8) vs. 1.8 (2.3), difference 0.50 (95% CI −0.45 to 1.45)

Long term (12 months): 2.5 (3.0) vs. 2.0 (2.5), difference 0.50 (95% CI −0.56 to 1.56)

Long term (24 months): 2.1 (2.8) vs. 2.7 (2.9)

ODI (0-100)

Baseline: 25.4 (10.6) vs. 23.8 (11.7)

Postintervention: 20.9 (10.1) vs. 21.6 (11.4), difference −0.70 (95% CI −4.60 to 3.20)

Intermediate term: 20.4 (11.6) vs. 18.0 (11.5), difference 2.4 (95% CI −1.87 to 6.67)

Long term (12 months): 18.9 (12.8) vs. 18.5 (12.4), difference 0.40 (95% CI −4.43 to 5.23)

Long term (24 months): 19.7 (14.3) vs. 19.3 (13.1), difference 0.40 (95% CI −5.20 to 6.00)

A vs. B, Mean (SD)

Symptoms of depression (DEPS) (0–30)

Baseline: 7.5 (5.2) vs. 6.7 (5.5)

Postintervention: 5.5 (5.5) vs. 5.7 (5.2), difference −0.20 (95% CI −2.13 to 1.73)

Intermediate term: 5.7 (4.6) vs. 5.8 (5.7), difference −0.10 (95% CI −2.01 to 1.81)

Long term (12 months): 6.6 (5.8) vs. 5.0 (4.0), difference 1.60 (95% CI −0.31 to 3.51)

Long term (24 months): 6.7 (5.3) vs. 5.7 (4.7), difference 1.00 (95% CI – 1.05 to 3.05)

A vs. B, Mean (SD)

Harms: NR

Number contacts to any health-care professional

Long term (12 months): 5.8 (9.9) vs. 5.4 (8.2), difference 0.40 (95% CI −3.08 to 3.88)

Long term (24 months): 3.4 (7.0) vs. 5.3 (8.6), difference −1.90 (95% CI −5.09 to 1.29)

Mangels, 2009

Germany

Mean duration of pain: NR

RCT

Fair

A. CPMP + booster sessions (n=119) ~4 weeks + 7, 20-minute booster sessions over 12 months, group + individual, inpatient

B. CPMP (n=113) ~4 weeks, group + individual, inpatient

C. PA (n=131) ~3.5 weeks, group + individual, inpatient

Mean age: 49 years

% Male: 22%

Race/Ethnicity: NR

Pain etiology/type

Dorsalgia: 84%

Other dorsopathies, 71%

Arthrosis: 34%

Disability: NR

Comorbidities: NR

A vs. B vs. C, Mean (SD)

PPS - Affective pain perception (14-56)

Baseline: 30.9 (9.4) vs. 30.9 (10.4) vs. 29.6 (9.0)

Postintervention: 23.4 (9.4) vs. 23.7 (9.2) vs. 22.9 (8.2)

A vs. C: difference 0.50 (95% CI −1.69 to 2.69)

B vs. C: difference 0.80 (95% CI −1.39 to 2.99)

12 months: 24.1 (9.8) vs. 25.5 (9.9) vs. 25.1 (9.6)

A vs. C: difference −0.10 (95% CI −3.50 to 1.50)

B vs. C: difference 0.40 (95% CI −2.14 to 2.94)

PPS - Sensory pain perception (10-40)

Baseline: 18.9 (5.9) vs. 18.5 (5.6) vs. 18.8 (5.9)

Postintervention: 15.9 (5.3) vs. 15.9 (5.2) vs. 16.4 (5.8)

A vs. C: difference −0.50 (95% CI −1.89 to 0.89)

B vs. C: difference −0.50 (95% CI −1.90 to 0.90)

Long term: 16.3 (5.7) vs. 17.0 (6.1) vs. 17.3 (6.1)

A vs. C: difference −1.0 (95% CI −2.53 to 0.53)

B vs. C: difference −0.30 (95% CI −1.89 to 1.29)

PDI (0-70)

Baseline: 26.9 (13.9) vs. 26.1 (11.8) vs. 24.8 (12.5)

Postintervention: 21.7 (13.3) vs. 20.3 (13.9) vs. 21.0 (13.1)

A vs. C: difference 0.70 (95% CI −2.59 to 3.99)

B vs. C: difference −0.70 (95% CI −4.12 to 2.71)

Long term: 22.6 (16.0) vs. 22.0 (14.0) vs. 20.6 (13.5)

A vs. C: difference 2.0 (95% CI −1.80 to 5.80)

B vs. C: difference 1.4 (95% CI −2.19 to 4.99)

A vs. B vs. C, Mean (SD)

SF-12 PCS (0-100)

Baseline: 33.5 (9.1) vs. 33.6 (7.4) vs. 33.9 (8.7)

Postintervention: 38.9 (9.4) vs. 39.3 (9.9) vs. 38.6 (8.6)

A vs. C: difference 0.30 (95% CI −1.94 to 2.54)

B vs. C: difference 0.70 (95% CI −1.63 to 3.03)

Long term: 38.4 (10.4) vs. 38.4 (9.7) vs. 38.4 (10.1)

A vs. C: difference 0 (95% CI −2.64 to 2.64)

B vs. C: difference 0 (95% CI −2.59 to 2.59)

SF-12 MCS (0-100)

Baseline: 43.9 (12.1) vs. 44.0 (11.1) vs. 44.5 (11.5)

Postintervention: 48.9 (12.1) vs. 50.8 (10.5) vs. 50.9 (10.5)

A vs. C: difference −2.0 (95% CI −4.82 to 0.82)

B vs. C: difference −0.10 (95% CI −2.76 to 2.56)

Long term: 45.6 (11.7) vs. 46.0 (11.2) vs. 45.0 (11.7)

A vs. C: difference 0.60 (95% CI −2.42 to 3.62)

B vs. C: difference 1.0 (95% CI – 2.00 to 4.00)

BDI (0-63)

Baseline: 11.4 (9.8) vs. 11.1 (10.1) vs. 10.1 (8.1)

Postintervention: 7.2 (7.8) vs. 6.7 (6.0) vs. 7.8 (7.8)

A vs. C: difference −0.60 (95% CI −4.08 to 2.88)

B vs. C: difference −1.10 (95% CI −4.56 to 2.36)

Long term: 10.7 (8.8) vs. 10.4 (7.8) vs.11.4 (8.2)

A vs. C: difference −0.70 (95% CI −2.89 to 1.49)

B vs. C: difference −1.0 (95% CI – 3.09 to 1.09)

A vs. B vs. C, Mean (SD)

Harms: One death during inpatient treatment (group A); no other details provided

German Life Satisfaction (with health)

Questionnaire (scale NR)

Baseline: 28.4 (9.5) vs. 28.1 (9.0) vs. 28.9 (8.5)

Postintervention: 33.1 (8.8) vs. 33.1 (9.2) vs. 32.5 (8.8)

A vs. C: 0.60 (95% CI −1.60 to 2.80)

B vs. C: 0.60 (95% CI −1.67 to 2.87)

Long term: 33.3 (9.5) vs. 31.7 (9.8) vs. 31.2 (8.4)

A vs. C: difference 2.1 (95% CI −0.21 to 4.41)

B vs. C: difference 0.50 (95% CI −1.87 to 2.87)

Meyer, 2005

Switzerland

RCT

Mean duration of pain: 36 months

Fair

A. CPMP (n=17)

8 weeks (17.5 hours/week, 140 hours total), session format NR for physical component, individual + group for psychological component, setting NR

B. PA (n=16) 8 weeks 1.5 hours/week (12 hours total), session format NR, outpatient

Median age: 43 years

Male: 79%

Race/Ethnicity: NR

Pain etiology/type:

Cervical, arm, and or head: 15%

Knee: 3%

Back and or leg: 69%

Widespread areas: 9%

Comorbidities: 1 or more, 39%

Other characteristics: To be included, patients needed to have Sick-leave for at least 2 months or 50% work incapacity from a full-time job over 3 months

A vs. B, Median (IQR)

Pain, NRS (0-10)

Baseline: 6.0 (3.5 to 7.0) vs. 5.5 (5.0 to 6.0)

Postintervention change score: 1.0 (−1.0 to 2.0) vs. 1.0 (0.0 to 2.0), p=0.34

PACT (scale NR)

Baseline: 82.0 (58.5 to 124.5) vs. 136.5 (74.8 to 160.8)

Postintervention change score: 10.0 (−9.0 to 37.0) vs. 3.0 (−10.0 to 36.0), p=0.60

A vs. B, Median (IQR)

SF-36 MCS (0-100)

Baseline: 32.0 (26.7 to 44.0) vs. 29.6 (25.2 to 37.4)

Postintervention change score: 6.0 (−5.4 to 12.9) vs. 2.5 (−3.6 to 11.9), p=0.90

SF-36 PCS (0-100)

Baseline: 30.0 (25.5 to 34.5) vs. 32.8 (28.4 to 37.4)

Postintervention change score: −0.4 (−3.8 to 2.6) vs. −4.4 (−9.0 to 0.4), p=0.17

A vs. B, % (n/N)

Harms

-

Pain in new localizations: 11.8% (2/17) vs. 31.2% (5/16), RR 0.38 (95% CI 0.08 to 1.7)

-

Other adverse reactions were not reported.

Roche, 2007, Roche-LeBoucher 2011

France

RCT

Mean duration of pain: NR (≥3 months)

Fair

A. CPMP (n=68)

5 weeks (6 hours/day, 150 hours total), group, outpatient

B. PA (n=64)

5 weeks (5 hours/week, ~25 hours total), individual, outpatient + home setting

Mean age: 40 years

% Male: 65%

Race/ethnicity: NR

Pain etiology/type: Chronic LBP

Disability:

-

Excluded if receiving disability pension.

Other characteristics:
-

Excluded if acute LBP or sciatica, spondylolisthesis, or cardiac or respiratory insufficiency, or psychiatric disorders preventing participation

A vs. B, Mean (SD)

VAS pain (0-10)

Baseline: 4.7 (2.1) vs. 4.5 (2.1)

Postintervention change score: −1.9 (NR) vs. −1.5 (NR)

Long term change score: −1.7 (2.6) vs. −1.0 (2.3), difference in change scores −0.70 (95% CI −1.64 to 0.24)

DPQ, daily activities (0%-100%)

Baseline: 51.8% (NR) vs. 51.0% (NR)

Postintervention change score: −21.5% (NR) vs. −17.2% (NR)

Long term change score: −20.3% (18.1%) vs. −10.4% (23.3%), difference in change scores −9.9 (95% CI −17.62 to −2.19)

A vs. B

DPQ, anxiety and depression (0%-100%)

Baseline: 36.9% (NR) vs. 30.9% (NR)

Postintervention change score: −17.6% (NR) vs. −7.4% (NR)

Long term change score: −15.6% (21.4%) vs. −4.8% (23.5%), difference in change scores −10.8 (95% CI −19.20 to −2.40)

Harms: one right tibial fracture in Group A which occurred at home; no other details provided

Ronzi, 2017

France

Mean duration of pain: NR (≥3 months)

RCT

Poor

A. CPMP (n=49)

5 weeks (30 hours/week; 150 hours total), group + individual, inpatient

B. CPMP (n=56)

5 weeks (11 hours/week; 55 hours total), group + individual, outpatient

C. PA (n=54)

Duration: 5 weeks (~5 hours/week, ~25 hours total), individual, outpatient + home setting

Mean age: 42 years

% Male: 59%

Race/ethnicity: NR

Pain etiology/type: Chronic LBP

Disability: NR

Other characteristics: NR

A vs. B vs. C, Median (IQR)

VAS pain (0-100)

Baseline: 54 (45 to 65) vs. 55 (36 to 68) vs. 45 (24 to 65)

Long term: 45 (25 to 59) vs. 37 (15 to 61) vs. 33 (19 to 48)

DPQ, daily activities (0%-100%)

Baseline: 63.0% (51.0% to 72.0%) vs. 57.0% (48.0% to 66.0%) vs. 54.0% (48.0% to 69.0%)

Long term: 51.0% (12.0% to 64.5%) vs. 39.0% (24.0% to 57.0%) vs. 54.0% (36.0% to 63.0%)

A vs. B vs. C, Median (IQR)

HADS (0-100)

Baseline: 17.0 (12.0 to 21.0) vs. 14.0 (11.0 to 18.0) vs. 16.0 (12.0 to 21.0)

Long term 11.5 (7.5 to 18.0) vs. 12.0 (7.0 to 15.0) vs. 13.0 (8.0 to 19.0)

A vs. C and B vs. C, p=ns

DPQ, anxiety and depression (0%-100%)

Baseline: 45.0% (20.0% to 60.0%) vs. 35.0% (25.0% to 45.0%) vs. 40.0% (15.0% to 55.0%)

Long term: 30.0% (5.0% to 45.0%) vs. 25.0% (5.0% to 45.0%) vs. 30.0% (5.0% to 45.0%)

SF-36 PCS (0-100)

Baseline: 35.7 (29.4 to 39.5) vs. 34.5 (30.7 to 39.2) vs. 35.6 (31.9 to 37.2)

Long term: 39.1 (33.8 to 50.4) vs. 41.6 (34.2 to 49.9) vs. 37.5 (33.0 46.8)

A vs. C and B vs. C, p=ns

SF-36 MCS (0-100)

Baseline: 43.3 (32.1 to 49.8) vs. 43.4 (35.9 to 51.1) vs. 41.2 (36.1 to 50.8)

Long term: 48.3 (42.1 to 53.4) vs. 46.6 (38.7 to 56.6) vs. 48.9 (41.4 to 54.8)

A vs. C and B vs. C, p=ns

Harms: No adverse effect related to the interventions was reported

Schweikert, 2006

Germany

RCT

Mean duration of pain: NR (≥6 months)

Fair

A. CPMP (n=200)

3 weeks hours total NR), group, inpatient

B. PA (n=209)

3 weeks hours total NR), group + individual, inpatient

Mean age: 47 years

Male: 83%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

Disability:

-

Sick listed <6 months in last year: 69%

-

Sick listed >6 months in last year: 6%

Comorbidities: NR

A vs. B, Mean (SD)

Back pain (scale 1-6)

Baseline: 4.3 (1.3) vs. 4.5 (1.2)

Postintervention change score: −1.2 (1.2) vs. −1.2 (1.2), difference in change scores 0 (95% CI −0.25 to 0.25)

Hannover functional questionnaire (FFbH) (0-100)

Baseline: 76.0 (19.2) vs. 72.2 (18.3)

Postintervention change score: 2.8 (12.3) vs. 3.5 (13.4), difference in change scores −0.70 (95% CI −3.37 to 1.97)

A vs. B, Mean (SD)

Depression (0-48)

Baseline: 8.3 (7.3) vs. 7.4 (6.3)

Postintervention change score: −2.3 (4.7) vs. −1.6 (4.2), difference in change scores −0.70 (95% CI −1.62 to 0.22)

STAI (20-80)

Baseline: 39.2 (10.4) vs. 38.8 (9.9)

Postintervention change score: −2.7 (6.9) vs. −2.3 (6.3), difference in change scores −0.40 (95% CI −1.78 to 0.98)

EQ-5D HRQOL (0-100)

Baseline: 60.8 (17.6) vs. 59.3 (16.6)

Postintervention: 70.3 (19.3) vs. 68.6 (19.5), difference 1.7 (95% CI −2.21 to 5.61)

Intermediate term: 70.0 (17.7) vs. 63.8 (19.9), difference 6.2 (95% CI 2.39 to 10.01)

NR

Smeets, 2006a, 2008

Netherlands

Mean duration of pain: 56.7 months

Cluster RCT

Fair

A. CPMP (n=61)

10 weeks (~75 hours total), group + individual, outpatient

B. PA (n=53)

10 weeks (~75 hours total), group + individual, outpatient

Mean age

42 years

Male: 53%

Race/ethnicity: NR

Mean duration of functional limitations: 35.1 months

Pain etiology/type: Chronic LBP

-

pain below knee: 49%

-

pain above knee: 37%

no leg pain: 14%

Disability pension:

-

Full 38%

-

Partial 24%

Previous back surgery: 15%

Trauma preceding LBP: 18%

A vs. B adjusted mean change score (SD) from baseline

VAS, current pain (0-10)

Baseline: 4.60 (2.40) vs. 5.12 (2.66)

Postintervention: adjusted difference in change scores: −0.018 (95% CI −0.934 to 0.899)

Intermediate term: adjusted difference in change scores: 0.498 (95% CI −0.429 to 1.425)

Long term: adjusted difference in change scores: 0.804 (95% CI −0.123 to 1.731)

Pain Rating Index Total (MPQ) (scale NR)

Baseline: 18.08 (9.04) vs. 18.34 (11.32)

Postintervention: adjusted difference in change scores: −0.95 (95% CI −4.59 to 2.98)

Intermediate term: adjusted difference in change scores: 1.97 (95% CI −1.71 to 5.65)

Long term: adjusted difference in change scores: 2.64 (95% CI −1.04 to 6.32)

RMDQ (0-23)

Baseline (mean, SD): 13.51 (3.92) vs. 14.15 (3.70))

Postintervention: adjusted difference in change scores: −0.05 (95% CI −1.71 to 1.62)

Intermediate term: adjusted difference in change scores: 0.62 (95% CI −1.06 to 2.30)

Long term: adjusted difference in change scores: 1.16 (–0.52 to 2.84)

VAS, main (activity) complaints (0-10)

Baseline: 7.24 (1.70) vs. 7.45

Postintervention: adjusted difference in change scores: −0.64 (95% CI −1.60 to 0.33)

Intermediate term: adjusted difference in change scores: −0.23 (95% CI −1.19 to 0.74)

Long term: adjusted difference in change scores: 0.03 (95% CI −0.94 to 1.00)

A vs. B adjusted mean change score (SD) from baseline

BDI (0-63)

Baseline: 9.75 (6.68) vs. 10.38 (7.62)

Postintervention: adjusted difference in change scores: 2.17 (95% CI 0.18 to 4.17)

Intermediate term: adjusted difference in change scores for group: 0.49 (95% CI −1.54 to 2.51)

Long term: adjusted difference in change scores: 1.05 (95% CI −0.97 to 3.07)

Global Improvement (1-7)

Postintervention: adjusted difference in change scores: 0.20 (95% CI – 0.35 to 0.75)

Intermediate term: adjusted difference in change scores: −0.38 (95% CI −0.94 to 0.18)

Long term: adjusted difference in change scores: −0.61 (95% CI −1.16 to −0.05)

A vs. B, % (n/N) or mean (SD)

Harms:

-

Increased low back pain or radiating leg pain leading to study withdrawal: 5.5% (3/55) vs. 5.8% (3/52); RR 0.95 (95% CI 0.20 to 4.48)

-

Herniated disc with neurological deficits needing neurosurgical intervention: 0% (0/55) vs. 1.9% (1/52) [one of the patients above]

-

Knee complaints causing patient to stop aerobic exercise: 0% (0/55) vs. 1.9% (1/52)

-

Pain complaints in both legs during cycling (vascular problems resolved by vascular surgery): 0% (0/55) vs. 1.9% (1/52)

VAS satisfaction (0-100)

(effect modification by RMDQ)

p=NS between groups except for in the 90th percentile strata of RMDQ.

Postintervention: adjusted difference: −21.58 (95% CI −39.56 to −3.59)

Turner, 1990

USA

Mean duration of pain: 12.9 years

RCT

Poor

A. CPMP (n=18)

8 weeks (4 hours/week, 32 hours total), group and individual, outpatient

B. PA (n=21)

8 weeks (2 hours/week, 16 hours total). group + individual, outpatient

Mean age: 44 years

Male: 52.1%

Race/ethnicity: White: 100%

Pain etiology/type: Chronic LBP

Disability: N/A

A vs. B, Mean (SD)

MPQ Pain Rating Index (0-78)

Baseline: 25.5 (12.41) vs. 19.4 (10.6)

Postintervention: 14.78 (11.44) vs. 17.51 (10.2), difference −2.73 (95% CI −9.75 to 4.29)

Intermediate term: 13.29 (9.15) vs.15.65 (9.15), difference −2.36 (95% CI −8.32 to 3.60)

Long term: 18.21 (13.31) vs. 14.94 (7.86), difference 3.27 (95% CI −3.70 to 10.24)

SIP (0-100)

Baseline: 8.50 (4.59) vs. 8.42 (8.21)

Postintervention: 3.63 (2.98) vs. 5.49 (6.79), difference −1.86 (95% CI −5.36 to 1.64)

Intermediate term: 4.51 (4.68) vs. 6.25 (10.08), difference −1.74 (95% CI −6.99 to 3.51)

Long term: 4.75 (3.40) vs. 4.73 (7.85) difference 0.02 (95% CI −4.02 to 4.06)

A vs. B, Mean (SD)

CES-D (0-60)

Baseline: 12.38 (7.31) vs. 11.95 (7.68)

Postintervention: 7.36 (5.89) vs. 7.38 (4.57), difference −0.02 (95% CI −3.42 to 3.38)

Intermediate term: 8.29 (7.94) vs. 9.29 (8.30), difference −1.0 (95% CI −6.30 to 4.30)

Long term: 10.00 (7.57) vs. 9.31 (7.73), difference 0.69 (95% CI – 4.29 to 5.67)

A vs. B, Mean (SD)

Harms: NR

Patient satisfaction (1-7): Postintervention: 5.50 (NR) vs. 4.48 (NR), p=NS

van Eijk-Hustings, 2013, 2016

Netherlands

Mean duration of pain: 6.8 years

RCT

Fair

A. CPMP (n=108)

12 weeks (36 days of sessions), group, outpatient

B. PA (n=47)

12 weeks (24 sessions), group, outpatient

Mean age 42 years

Male: 4%

Race/Ethnicity: NR

Pain etiology/type: FM

Disability: NR

Estimated marginal means (SD), A vs. B

FIQ, Pain

Baseline: 6.3 (2.1) vs. 6.2 (1.8)

Postintervention: 5.5 (2.1) vs. 5.3 (2.1), difference 0.20 (95% CI −0.53 to 0.93

Long term: 5.3 (2.1) vs. 5.2 (2.5) difference 0.10 (95% CI −0.67 to 0.87)

FIQ Total

Baseline: 64.5 (14.6) vs. 60.0 (14.4)

Postintervention: 55.1 (15.6) vs. 53.2 (16.5), difference 1.90 (95% CI −3.58 to 7.38

Long term: 50.9 (20.8) vs. 52.0 (21.9), difference −1.1 (95% CI −8.40 to 6.20)

Estimated marginal means (SD), A vs. B

EQ-5D (scale −0.59 to 1)

Baseline: 0.36 (0.3) vs. 0.41 (0.3)

Postintervention): 0.49 (0.3) vs. 0.47 (0.3), difference 0.02 (95% CI −0.08 to 0.12

Long term: 0.55 (0.3) vs. 0.54 (0.3), difference 0.01 (95% CI −0.09 to 0.11

FIQ, Depression

Baseline: 5.2 (3.1) vs. 4.8 (2.1)

Postintervention: 4.1 (3.1) vs. 4.6 (2.7), difference −0.50 (95% CI −1.53 to 0.53

Long term: 3.9 (3.1) vs. 5.0 (3.4), difference −1.1 (95% CI −2.20 to 0.002)

FIQ, Anxiety

Baseline: 5.9 (3.1) vs. 4.9 (2.1)

Postintervention: 5.0 (2.1) vs. 4.6 (2.7), difference 0.40 (95% CI −0.39 to 1.19

Long term: 4.7 (3.1) vs. 5.0 (3.4), difference −0.30 (95% CI −1.40 to 0.80

Estimated marginal means (SD), A vs. B

Harms: NR

A vs. B

Contact with GPs a

Baseline: 2.3 (3.1) vs. 3.3 (5.5)

Long term: 0.9 (2.1) vs. 0.7 (2.1), difference 0.20 (95% CI −0.53 to 0.93

Contact with medical specialists a

Baseline: 1.9 (1.0) vs. 1.9 (1.4)

Long term: 0.3 (1.0) vs. 0.4 (0.7), difference – 0.10 (95% CI −0.42 to 0.22

Contact with physiotherapists a

Baseline: 2.7 (5.2) vs. 1.9 (1.4)

Long term: 2.6 (5.2) vs. 0.4 (0.7) difference 2.20 (95% CI 0.69 to 3.71)

Contact with other paramedical professionals a

Baseline: 1.1 (3.1) vs. 1.1 (2.7)

Long term: 1.0 (3.1) vs. 2.1 (3.4), difference – 1.10 (95% CI −2.20 to 0.002)

BDI = Beck Depression Inventory; CES-D = Center for Epidemiological Studies Depression; CI = confidence interval; CPMP = comprehensive pain management program; EQ-5D = EuroQol 5Dimensions; FIQ = Fibromyalgia Impact Questionnaire; FM = fibromyalgia; HADS = Hospital Anxiety and Depression Scale; HRQOL = health-related quality of life; IP = Inpatient; LBP = low back pain; MCS = Mental component summary score (of the SF-12 or SF-36); MVAS = Million visual analog scale; NR = not reported; NS = not statistically significant; ODI = Oswestry Disability Index; OP = outpatient; PA = physical activity; PACT = Performance Assessment of Capacity Testing; PCS = Physical component summary score (of the SF-12 or SF-36); PDI = Pain Disability Index; PPS = Pain Perception Scale; RCT = randomized controlled trial; SIP = Sickness Impact Profile; SD = standard deviation; SF-36 = Short-Form 36 questionnaire; STAI = State-Trait Anxiety Inventory; VAS = visual analog scale

a

Total number of consultations over a period of 2 months prior to measurement

Table B-7Summary results for trials addressing KQ1: CPMPs versus pharmacologic therapy alone

Author, Year

Country

Pain Duration

Study Design

Study Quality

Intervention (n), Comparator (n), Duration/Intensity, Session Format, SettingPopulation

Primary Outcomes:

Pain, Function, and Opioid Use

Secondary Outcomes:

HRQOL, Psychological Measures, Global Improvement

Harms

Utilization

Patient Satisfaction

Castel, 2013, 2015, Salvat, 2017

Spain

Mean pain duration: 140 months

RCT

Fair

A. Comprehensive pain management program (n=74)

12 weeks, 4 hours/week, 48 hours total, group, outpatient

B. Pharmacological therapy only (n=81)

12 weeks, Analgesics, antidepressants, benzodiazepine and nonbenzodiazepine hypnotics (dosages NR); adjusted as recommend by guidelines

Mean age: 49 years

% Female: 100%

Race/Ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability: NR

-

Receiving workers compensation: 6%

Comorbidities: NR

A vs. B, Mean (SD) (unless otherwise stated)

Proportion of patients meeting the MCID of 30% improvement on the NRS, % (n’s and N’s NR)

Posttreatment: 22.2% (18/81) vs. 6.7% (5/74), RR 3.3 (95% CI 1.3 to 8.4)

Short term: 13.6% (11/81) vs. 10.8% (8/74), RR 1.3 (95% CI 0.53 to 3.0)

Intermediate term: 16.0% (13/81) vs. 5.4% (4/74), RR 3.0 (95% CI 1.0 to 8.7)

Long term: 8.6% (7/81) vs. 0% (0/74), RR not calculable

Pain NRS (0 to 10)

Baseline: 6.8 (1.4) vs. 7.1 (1.6)

Posttreatment: 5.7 (1.9) vs. 6.9 (1.8), difference −1.2 (95% CI −7.8 to −0.61)

Short term: 6.4 (1.9) vs. 6.8 (1.8), difference −0.40 (95% CI −0.99 to 0.19)

Intermediate term: 6.4 (1.9) vs. 7.0 (1.9), difference −0.60 (95% CI −1.2 to 0.00)

Long term: 6.7 (1.6) vs. 7.1 (1.8), difference −0.40 (95% CI −0.94 to 0.14)

Proportion of patients meeting the MCID of 14% improvement on the FIQ, % (n/N)

Posttreatment: 64.2% (52/81) vs. 24.3% (18/74), RR 2.6 (95% CI 1.7 to 4.1)

Short term: 48.1% (39/81) vs. 23.0% (17/74), RR 2.1 (95% CI 1.3 to 3.4)

Intermediate term: 42.0% (34/81) vs. 18.9% (14/74), RR 2.2 (95% CI 1.3 to 3.8)

Long term: 27.2% (22/81) vs. 4.0% (3/74), RR 6.7 (95% CI 2.1 to 21.5)

FIQ (0 to 100)

Baseline: 64.6 (16.0) vs. 66.6 (17.4)

Posttreatment: 47.7 (20.2) vs. 65.9 (16.1), difference −18.2 (95% CI −24.0 to −12.4)

Short term: 55.5 (19.3) vs. 64.6 (17.6), difference −9.1 (95% CI −15.0 to −3.2)

Intermediate term: 55.8 (20.9) vs. 67.8 (18.4), difference −12.0 (95% CI −18.3 to −5.7)

Long term: 58.8 (20.5) vs. 69.6 (17.2), difference −10.8 (95% CI −16.8 to −4.8)

COOP/WANCA physical function subscale (0 to 5)

Baseline: 3.0 (0.84) vs. 3.3 (0.77)

Posttreatment: 2.4 (0.76) vs. 3.3 (0.72), difference −0.90 (95% CI −1.1 to −0.65)

Short term: 2.7 (1.2) vs. 3.2 (0.61), difference −0.50 (95% CI −0.84 to −0.16)

Intermediate term: 2.7 (0.74) vs. 3.4 (0.91), difference −0.70 (95% CI −0.99 to −0.41)

Long term: 2.7 (0.86) vs. 3.3 (0.57), difference −0.60 (95% CI −0.93 to – 0.27)

COOP/WANCA daily activities subscale (1 to 5)

Baseline: 3.3 (0.47) vs. 3.4 (0.43)

Posttreatment: 2.8 (0.43) vs. 3.1 (0.40), difference −0.30 (95% CI −0.44 to −0.16)

Short term: 2.9 (0.43) vs. 3.2 (0.61), difference −0.30 (95% CI −0.48 to −0.12)

Intermediate term: 3.0 (0.42) vs. 3.3 (0.58), difference −0.30 (95% CI −0.47 to −0.12)

Long term: 2.9 (0.55) vs. 3.3 (0.57), difference −0.40 (95% CI −0.64 to – 0.16)

Authors found no significant interactions in BMI × time, and in BMI × group treatment × time. There are not differences among normal weight, overweight, and obese patients with FM regarding their response to a CPMP for any of the outcomes listed above.

A vs. B, Mean (SD)

COOP/WANCA measure of HRQOL (9-45)

Baseline: 26.8 (32.9) vs. 28.0 (27.7)

Posttreatment: 22.1 (29.7) vs. 26.7 (28.0), difference −5.9 (95% CI −16.0 to 4.2)

Short term: 23.8 (29.7) vs. 26.5 (28.0), difference −2.7 (95% CI −12.8 to 7.3)

Intermediate term: 23.7 (28.9) vs. 27.3 (26.6), difference −3.6 (95% CI −13.5 to 6.2)

Long term: 23.4 (25.1) vs. 26.5 (21.9), difference −3.1 (95% CI −13.4 to 7.2)

HADS (scale NR)

Baseline: 21.9 (8.0) vs. 23.2 (8.1)

Posttreatment: 14.3 (9.0) vs. 21.7 (8.4), difference −7.4 (95% CI −10.2 to −4.6)

Short term: 15.2 (9.1) vs. 20.6 (8.5), difference −5.4 (95% CI −8.2 to −2.6)

Intermediate term: 16.2 (9.3) vs. 21.5 (8.5), difference −5.3 (95% CI −8.1 to −2.5)

Long term: 17.1 (9.9) vs. 22.8 (9.2), difference −5.7 (95% CI −8.7 to −2.7)

Authors found no significant interactions in BMI × time, and in BMI × group treatment × time. There are not differences among normal weight, overweight, and obese patients with FM regarding their response to a CPMP for any of the outcomes listed above.

NR

Martin, 2014a, 2014b, 2014c

Spain

Mean duration of pain: 170 months

RCT

Poor

A. Comprehensive pain management program (n=54)

6 weeks, 2.75 hours/week, 16.5 hours total, session format NR, outpatient

B. Pharmacological therapy only (n=56)

6 weeks, Amitriptyline (maximum dose 75 mg/day), Paracetamol, (maximum dose 4 g/day), Tramadol, (maximum dose 400 mg/day)

Mean age: 50 years

% Male: 9%

Race/Ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability: 15%

Comorbidities:

-

Hypothyroidism: 12%

-

High blood pressure: 10%

-

COPD: 12%

-

Diabetes mellitus: 3%

-

Rheumatoid arthritis: 3%

-

Other: 42%

A vs. B, Mean (SD)

VAS current pain (0 to 10)

Baseline: 6.76 (1.98) vs. 7.06 (2.04)

Intermediate term: 5.99 (2.37) vs. 7.21 (1.56), difference −1.2 (95% CI −2.0 to – 0.46)

FIQ Total (0 to 100)

Baseline: 76.28 (13.17) vs. 76.23 (14.80)

Intermediate term: 70.33 (16.98) vs. 76.81 (14.18), difference −6.5 (95% CI −12.4 to −0.58)

A vs. B, Mean (SD)

FIQ depression subscale (0 to 10)

Baseline: 6.90 (3.06) vs. 7.20 (2.83)

Intermediate term: 6.44 (3.13) vs. 6.61 (3.14), difference −0.17 (95% CI −1.4 to 1.0)

HADS depression (0 to 21)

Baseline: 10.63 (4.57) vs. 10.57 (4.06)

Intermediate term: 9.77 (4.09) vs. 10.25 (4.22), difference −0.48 (95% CI −2.1 to 1.1)

HADS anxiety (0 to 21)

Baseline: 13.13 (3.39) vs. 13.39 (3.45)

Intermediate term: 13.49 (4.31) vs. 12.75 (4.55), difference 0.74 (95% CI −0.94 to 2.4)

NR

Onac, 2012, 2017

Romania

Mean duration of pain: NR

RCT

Poor

A. Comprehensive pain management program (n=29)

2 weeks, 5 days/week (total hours NR), individual, inpatient

B. Pharmacological therapy (n=20)

2 weeks, Diclofenac (50mg, 3 times/day), Omeprazole (20 mg, 1 time/day), and Acetaminophen (1000 mg, 4 times/day)

Population data include patients from the third arm of this trial

Mean age: 47 years

% Male: 57%

Race/ethnicity: NR

Pain etiology/type: Lumbar disk hernia

Disability: NR

Other characteristics:

-

Excluded: history of psychotic disorders, substance abuse disorders, certain personality disorders.

A vs. B Mean (SD)

VAS pain (0 to 10)

All patients

Baseline: 3.83 (1.89) vs. 5.77 (2.55)

Postintervention (2 weeks): 3.02 (1.94) vs. 4.73 (2.67), difference −1.71 (95% CI −3.0 to −0.39)

Nonclinical catastrophizers

Baseline: 3.12 (1.70) vs. 4.67 (2.56)

Postintervention (2 weeks): 1.78 (1.14) vs. 3.65 (2.44), difference −1.87 (95% CI −3.3 to −0.45)

Clinical catastrophizers

Baseline: 4.32 (2.00) vs. 7.80 (1.39)

Postintervention (2 weeks): 3.77 (1.91) vs. 6.60 (2.45), difference −2.83 (95% CI −4.8 to −0.83)

RMDQ (0 to 24)

All patients

Baseline: 10.66 (6.73) vs. 9.95 (5.75)

Postintervention (2 weeks): 8.66 (7.11) vs. 8.90 (6.406), difference −0.24 (95% CI −4.2 to 3.8)

A vs. B Mean (SD)

POMS-SV Emotional Distress (scale NR)

All patients

Baseline: 46.03 (26.52) vs. 39.85 (21.52)

Postintervention (2 weeks): 43.15 (31.16) vs. 37.94 (21.01), difference 5.2 (95% CI −10.9 to 21.3)

NR

Tavafian, 2011, 2014, 2017a, 2017b

Iran

Mean duration of pain: 82.2 months

RCT

Fair

A. Comprehensive pain management program (n=97)

1 week + monthly booster sessions, 69 hours total, session format NR, outpatient

B. Pharmacologic therapy alone (n=100)

Analgesics, NSAIDS, muscle relaxants, and antidepressant drugs

Mean age: 45 years

% Male: 26.08%

Race/ethnicity: NR

Pain etiology/type: Chronic LBP

Disability: NR

Comorbidities:

-

% Smokers: 5.6%

Other characteristics:
-

% with sciatica: 85.8%

-

Excluded: back surgery within last 2 years

A vs. B, Mean (SD)

QDS (0 to 100)

Baseline: 35.45 (20.19) vs. 33.08 (19.69)

Short term: 23.48 (18.54) vs. 32.70 (18.19), difference −9.2 (95% CI −14.5 to −3.9)

Intermediate term: 18.65 (16.14) vs. 27.19 (17.85), difference −8.5 (95% CI −13.4 to −3.6)

Long term (12 months): 17.4 (16.4) vs. 24.4 (18.3), difference −7.0 (95% CI – 12.1 to −1.9)

Long term (18 months): 17.56 (15.62) vs. 23.80 (18.53), difference −6.2 (95% CI −11.9 to −0.60)

Long term (24 months): 15.36 (16.22) vs. 23.32 (17.74), difference −8.0 (95% CI −13.5 to −2.4)

Long term (30 months): 15.85 (16.39) vs. 21.41 (17.21), difference −5.6 (95% CI −11.1 to −0.05)

RMDQ (0 to 24)

Baseline: 9.80 (5.07) vs. 10.04 (5.28)

Short term: 9.01 (5.71) vs. 10.56 (5.78), difference −1.6 (95% CI −3.2 to 0.10)

Intermediate term: 7.03 (5.49) vs. 8.80 (5.68), difference −1.8 (95% CI −3.4 to −0.17)

Long term (12 months): 6.01 (5.8) vs. 8.9 (6.6), difference −2.89 (95% CI −4.5 to −1.2)

Long term (18 months): 5.86 (5.62) vs. 8.97 (6.54), difference −3.1 (95% CI −5.1 to −1.1)

Long term (24 months): 5.62 (5.89) vs. 7.88 (5.90), difference −2.3 (95% CI −4.2 to −0.33)

Long term (30 months): 5.52 (5.89) vs. 7.71 (6.35), difference −2.2 (95% CI – 4.2 to −0.18)

A vs. B, Mean (SD)

SF-36, Physical function (0 to 100) a

Baseline: 54.61 (23.27) vs. 54.53 (23.30)

Short term: 68.64 (23.39) vs. 60.93 (22.04), difference 7.7 (95% CI 1.2 to 14.3)

Intermediate term: 77.77 (18.71) vs. 63.698 (21.88), difference 14.1 (95% CI 8.2 to 19.9)

Long term (12 months): 80.3 (18.6) vs. 64.4 (22.8), difference 15.9 (95% CI 9.7 to 22.1)

SF-36, Role physical (0 to 100) a

Baseline: 30.70 (33.98) vs. 32.81 (36.86)

Short term: 57.88 (68.33) vs. 39.58 (36.93), difference 18.3 (95% CI 2.6 to 34.0)

Intermediate term: 66.03 (36.79) vs. 47.13 (39.04), difference 18.9 (95% CI 8.0 to 29.8)

Long term (12 months): 72.4 (37.3) vs. 56.04 (38.3), difference 16.3 (95% CI 5.2 to 27.6)

SF-36, Bodily pain (0 to 100) a

Baseline: 43.27 (22.59) vs. 47.45 (23.59)

Short term: 65.82 (22.56) vs. 56.35 (23.62), difference 9.5 (95% CI 2.8 to 16.1)

Intermediate term: 72.34 (22.77) vs. 60.27 (25.82), difference 12.1 (95% CI 5.1 to 19.1)

Long term (12 months): 69.5 (18.3) vs. 56.2 (21.3), difference 13.3 (95% CI 7.4 to 19.2)

SF-36, General health (0 to 100) a

Baseline: 50.41 (20.16) vs. 49.92 (19.80)

Short term: 59.67 (21.59) vs. 52.65 (23.34), difference 7.0 (95% CI 0.69 to 13.3)

Intermediate term: 61.01 (21.96) vs. 53.29 (22.83), difference 7.7 (95% CI 1.3 to 14.2)

Long term (12 months): 69.6 (21.7) vs. 59.9 (24.3), difference 9.7 (95% CI 2.9 to 16.5)

SF-36,Vitality (0 to 100) a

Baseline: 53.58 (19.22) vs. 53.95 (20.02)

Short term: 60.10 (23.25) vs. 55.05 (20.74), difference 5.1 (95% CI −1.3 to 11.4)

Intermediate term: 65.70 (22.25) vs. 59.84 (22.35), difference 5.9 (95% CI −0.56 to 12.3)

Long term (12 months): 70.3 (22.5) vs. 63.1 (22.5), difference 7.2 (95% CI 0.54 to 13.9)

SF-36, Mental health (0 to 100) a

Baseline: 47.43 (13.96) vs. 44.00 (13.10)

Short term: 65.13 (21.59) vs. 57.70 (23.22), difference 7.4 (95% CI 0.97 to 13.9)

Intermediate term: 66.04 (23.67) vs. 61.41 (23.25), difference 4.6 (95% CI −2.1 to 11.4)

Long term (12 months): 71.8 (20.2) vs. 58.9 (24.9), difference 12.9 (95% CI 6.2 to 19.6)

SF-36, Role emotional (0 to 100) a

Baseline: 38.04 (40.32) vs. 49.65 (44.580)

Short term: 50.72 (45.15) vs. 41.31 (44.25), difference 9.4 (95% CI −3.5 to 22.3)

Intermediate term: 58.33 (45.99) vs. 52.43 (47.07), difference 5.9 (95% CI −7.5 to 19.3)

Long term (12 months): 72.4 (42.3) vs. 53.1 (46.6), difference 19.3 (95% CI 6.1 to 32.5)

SF-36, Social Function (0 to 100) a

Baseline: 62.22 (24.65) vs. 63.02 (28.55)

Short term: 59.78 (21.12) vs. 51.77 (21.20), difference 8.0 (95% CI 1.9 to 14.1)

Intermediate term: 76.90 (23.50) vs. 69.37 (26.65), difference 7.5 (95% CI 0.30 to 14.8)

Long term (12 months): 81.6 (19.3) vs. 70.05 (27.4), difference 11.6 (95% CI 4.5 to 18.6)

NR

Tavaflan, 2008

Iran

Mean duration of pain: 9.07 months

RCT

Fair

A. Comprehensive pain management program (n=50)

4 days, intensity NR, individual, outpatient

B. Pharmacological therapy alone (n=52)

Acetaminophen, NSAID and chlordiazepoxide

Mean age: 44 years

% Female: 100%

Race/ethnicity: NR

Pain etiology/type: Chronic LBP

Disability: NR

Comorbidities:

-

% Smokers: 3.9%

NR

A vs. B, Mean (SD)

SF-36 PCS (0 to 100)

Baseline: 44.3 (16.8) vs. 42.6 (24.0)

Short term: 76.7 (17.3) vs. 51.2 (28.1), difference 25.5 (95% CI 14.9 to 36.3)

Intermediate term: 66.6 (27.5) vs. 51.2 (28.8), difference 15.4 (95% CI 2.4 to 28.5)

Long term: 64.7 (36.3) vs. 51.1 (28.3), difference 13.6 (95% CI −1.5 to 28.7)

SF-36 MCS (0 to 100)

Baseline: 47.7 (28) vs. 49.5 (23.1)

Short term: 80.4 (22.8) vs. 57.4 (29.5), difference 23.0 (95% CI 10.8 to 35.2)

Intermediate term: 66.9 (29.9) vs. 57.9 (25.5), difference 9.0 (95% CI −3.9 to 21.9)

Long term: 65.1 (27.2) vs. 60.2 (26.6), difference 4.9 (95% CI −7.6 to 17.4)

NR

BMI = body mass index; CI = confidence interval; COOP/WANCA = Dartmouth Primary Care Cooperative Information Project/World Organization of National Colleges, Academies, and Academic Associations of General Practice/Family Physicians; FIQ = Fibromyalgia Impact Questionnaire; HADS = Hospital Anxiety and Depression Scale; HRQOL = health-related quality of life; LBP = low back pain; MCID = Minimally clinically important difference; MD = mean difference; NR = not reported; NRS = Numeric Rating Scale; NRS = numeric rating scale; NSAIDS = nonsteroidal anti-inflammatory; POMS-SV = Profile of Mood States Short Version; QDS = Quebec Back Pain Disability Scale; QOL = quality of life; RCT = randomized control trial; RMDQ = Roland Morris Disability Questionnaire; RR = risk ratio; SD = standard deviation; SF-36 = short form 36 item questionnaire; VAS = Visual Analog Scale.

a

Only 12-month data for long term followup are reported here. For long term followup at 18, 24, and 30 months, see the full data abstraction appendix.

Table B-8Summary results for trials addressing KQ1: CPMPs versus pharmacologic therapy plus physical activity

Author, Year

Country

Pain Duration

Study Design

Study Quality

Intervention (n)

Comparator (n)

Duration/Intensity Session Format Setting

Population

Primary Outcomes:

Pain, Function, and Opioid Use

Secondary Outcomes:

HRQOL, Psychological Measures, Global Improvement

Harms

Utilization

Patient Satisfaction

Thieme 2003

Germany

Mean duration of pain: 195.7 months

RCT

Fair

A. Comprehensive pain management program (n=42)

5 weeks, 75 hours total, combination of individual and group, inpatient

B. Physical Activity + Pharmacological therapy (n=21)

5 weeks, Antidepressants, physical component not well described, mostly passive

Mean age: 48 years

% Male: 0% (female only for inclusion)

Race/ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability: NR

Other characteristics:

-

Patients were excluded if they had inflammatory cause of the pain, neurologic complications, duration of pain less than 4 months, pregnancy, another severe disease such as a tumor, liver, or renal disease, major psychiatric disorders.

A vs. B, Mean (SD)

MPI, Pain intensity (0 to 6)

Baseline: 4.43 (0.98) vs. 4.34 (1.11)

Postintervention: 3.82 (0.96) vs. 5.47 (1.06), difference −1.7 (95% CI −2.2 to −1.1)

Intermediate term: 3.66 (1.22) vs. 4.85 (0.86), difference −1.2 (95% CI −1.8 to −0.59)

Long term: 3.18 (1.27) vs. 5.28 (0.83), difference – 2.1 (95% CI −2.7 to −1.5)

MPI, Interference (0 to 6)

Baseline: 4.35 (1.01) vs. 4.43 (0.91)

Postintervention: 3.29 (1.02) vs. 5.28 (0.86), difference −2.0 (95% CI −2.5 to −1.5)

Intermediate term: 2.96 (1.18) vs. 4.83 (0.72), difference −1.9 (95% CI −2.4 to −1.3)

Long term: 2.79 (1.37) vs. 5.33 (0.81), difference – 2.5 (95% CI −3.2 to −1.9)

MPI, Total activity (0 to 6)

Baseline: 2.53 (0.78) vs. 2.89 (0.91)

Postintervention: 2.65 (0.65) vs. 2.90 (0.92), difference −0.25 (95% CI −0.66 to 0.16)

Intermediate term: 2.68 (0.81) vs. 2.90 (0.93), difference −0.22 (95% CI −0.68 to 0.24)

Long term: 2.63 (0.70) vs. 2.90 (0.93), difference – 0.27 (95% CI −0.69 to 0.15)

A vs. B, Mean (SD)

MPI, Affective distress (0 to 6)

Baseline: 3.69 (1.33) vs. 3.72 (1.57)

Postintervention: 2.54 (1.03) vs. 4.46 (1.48), difference −1.9 (95% CI −2.6 to −1.3)

Intermediate term: 2.38 (1.29) vs. 4.47 (1.65), difference −2.1 (95% CI −2.9 to −1.3)

Long term: 2.46 (1.28) vs. 4.78 (1.60), difference −2.3 (95% CI −3.1 to −1.6)

A vs. B, mean (SD)

Program-related outcomes:

Number of doctor visits:

Baseline: 31.61 (19.88) vs. 28.60 (18.40)

15 months: 14.70 (9.90) vs. 37.8 (22. 03), difference 3.0 (95% CI −7.4 to 13.5)

Number of days at the hospital:

Baseline: 13.24 (22.96) vs. 10.35 (14.76)

15 months: 2.61 (6.34) vs. 18.65 (17.82), difference −16.04 (95% CI – 22.3 to −9.8)

Onac, 2012 & 2017

Romania

Mean duration of pain: NR

RCT

Poor

A. Comprehensive pain management program (n=29)

2 weeks, 5 days/week (total hours NR), individual, inpatient

B. Physical Activity + Pharmacological therapy (n=26)

2 weeks (total hours NR), Diclofenac (50mg, 3 times/day), Omeprazole (20 mg, 1 time/day), and Acetaminophen (1000 mg, 4 times/day) physical component not well described, mostly passive

Population data include patients from the third arm of this trial

Mean age: 47 years

% Male: 57%

Race/ethnicity: NR

Pain etiology/type: Lumbar disk hernia

Disability: NR

Other characteristics: Patients were excluded if they had history of psychotic disorders, substance abuse disorders in past Short term, or certain personality disorders.

A vs. B, Mean (SD)

VAS pain (0 to 10)

All patients

Baseline: 3.83 (1.89) vs. 4.58 (2.59)

Postintervention (2 weeks): 3.02 (1.94) vs. 2.086 (2.17), difference 0.93 (95% CI −0.19 to 2.1)

Nonclinical catastrophizers

Baseline: 3.12 (1.70) vs. 3.53 (2.47)

Postintervention (2 weeks): 1.78 (1.14) vs. 1.52 (1.82), difference 0.26 (95% CI −0.83 to 1.3)

Clinical catastrophizers

Baseline: 4.32 (2.00) vs. 6.45 (1.60)

Postintervention (2 weeks): 3.77 (1.91) vs. 3.07 (2.49), difference 0.70 (95% CI −1.3 to 2.7)

RMDQ (0 to 24)

All patients

Baseline: 10.66 (6.73) vs. 11.16 (5.82)

Postintervention (2 weeks): 8.66 (7.11) vs. 7.16 (5.23), difference 1.5 (95% CI −2.0 to 5.0)

A vs. B, Mean (SD)

POMS-SV Emotional Distress (scale NR)

All patients

Baseline: 46.03 (26.52) vs. 45.16 (28.09)

Postintervention (2 weeks): 43.15 (31.16) vs. 41.90 (32.18), difference 1.25 (95% CI −16.1 to 18.6)

NR

CI = confidence interval; FIQ = Fibromyalgia Impact Questionnaire; HRQOL = health-related quality of life; MD = mean difference; MPI = Multidimensional Pain Inventory; NR = not reported; POMS-SV = Profile of Mood States Short Version; RCT = randomized control trial; RMDQ = Roland Morris Disability Questionnaire; SD = standard deviation; VAS = Visual Analog Scale

Table B-9Summary results for trials addressing KQ1: CPMPs versus psychological therapy

Author, Year

Country

Pain Duration

Study Design

Study Quality

Intervention (n)

Comparator (n)

Duration/Intensity Session Format Setting

Population

Primary Outcomes:

Pain, Function, and Opioid Use

Secondary Outcomes:

HRQOL, Psychological Measures, Global Improvement

Harms

Utilization

Patient Satisfaction

Jensen, 2001

Sweden

Duration of pain: 31 months

RCT

Fair

A. Comprehensive pain management program, (n=63): 4 weeks (33-34 hours/week, plus six 90-minute booster sessions over a period of 1 year after treatment); high intensity, group; Rehabilitation clinic

B. Psychological Therapy (n=49): 4 weeks, (13-14 hours/week, plus six 90-minute booster sessions over a period of 1 year after treatment); low intensity, group in person; Rehabilitation clinic

Mean age: 43 years

Male: 45%

Race/ethnicity: Swedish origin 67%

Pain etiology/type: Chronic nonspecific spinal pain

-

Cervical/thoracic pain: 42%

-

Lumbar pain: 46%

-

Mixed pain areas: 12%

Disability: NR
-

Mean total sick leave in 6 months prior to inclusion in study: 292 (63)

Comorbidities:
-

NR

NR

A vs. B, Mean (SD)

SF-36 Global health (0-100)

Females only (n=30 vs. 22)

Baseline: 38.1 (14.5) vs. 38.9 (13.7)

Postintervention: 47.6 (18.0) vs. 48.8 (16.8)

Intermediate term: 52.4 (21.6) vs. 54.2 (19.3)

Long term: 53.1 (24.5) vs. 58.2 (18.4)

-

improvement approached significance for group B at Long term(p=0.057)

Males only (n=33 vs. 27)

Baseline: 41.6 (14.6) vs. 43.8 (16.0)

Postintervention: 48.5 (17.2) vs. 44.8 (18.0)

Intermediate term: 54.3 (18.3) vs. 43.5 (19.1))

Long term: 57.2 (21.8) vs. 50.8 (27.9)

-

Nonsignificant group effect via MANCOVA with a repeated-measures design

-

p=ns between interventions at any timepoint

A vs. B, Mean (SD)

Harms: NR

Perceived appropriateness of the treatment program to treating patient’s pain (0-10)

Females only (n=30 vs. 22)

Postintervention: 6.4 (3.1) vs. 4.8 (3.7), p=ns

Males only (n=33 vs. 27)

Postintervention: 6.0 (3.6) vs. 4.5 (3.2), p=ns

Likelihood of recommending treatment program to a relative with a similar pain condition (0-10)

Females only (n=30 vs. 22)

Postintervention: 7.0 (3.7) vs. 6.0 (3.8), p=ns

Males only (n=33 vs. 27) A vs. B

Postintervention: 6.1 (4.3) vs. 5.1 (4.2), p=ns

Linton, 2005

Sweden

Pain duration: NR (>12 weeks: 84%)

RCT

Fair

A. Comprehensive pain management program, (n=69): 6 weeks (hours not reported, at least 12 total); low intensity, group; Primary care (outpatient)

B. Psychological Therapy (n=47): 6 weeks, (2 hour session); low intensity, group; outpatient

Mean age: 48 years

Male: 16%

Race/ethnicity: NR

Pain etiology/type:

-

Chronic back pain: 90%

-

Chronic neck pain: 10%

Disability: NR

Comorbidities: NR

A vs. B, Mean (SD)

Pain Numeric Rating Scale (0-10)

Average pain last week:

Baseline: 4.4 (2.1) vs. 4.2 (2.5)

Long term: 2.9 (2.2) vs. 3.4 (2.4); difference −0.5 (95% CI −1.35 to 0.35)

Average pain last 3 months:

Baseline: 4.5 (1.9) vs. 4.5 (2.1)

Long term: 3.0 (1.8) vs. 3.2 (2.4); difference −0.2 (95% CI −0.98 to 0.58)

Worst pain last 3 months:

Baseline: 6.0 (2.3) vs. 5.6 (2.5)

Long term: 4.3 (2.9) vs. 4.5 (3); difference −0.2 (95% CI −1.29 to 0.89)

Pain-free days in last week (0-7)

Baseline: 2.3 (2.5) vs. 1.9 (3.0)

Long term: 3.5 (3.0) vs. 3.2 (3); difference 0.3 (95% CI −0.81 to 1.41)

Activities of Daily Living (0-50)

Baseline: 38.9 (10.0) vs. 38.9 (12.3)

Long term: 41.5 (10.4) vs. 42.6 (7.9); difference −1.10 (95% CI – 4.55 to 2.35)

RMDQ (0-18)

Baseline: 3.7 (4.5) vs. 3.4 (5.1)

Long term: 3.4 (4.2) vs. 3.2 (4.1); difference 0.2 (95% CI −1.33 to 1.74)

A vs. B, Mean (SD)

HADS Anxiety (0-21)

Baseline: 4.9 (3.8) vs. 5.3 (5.1)

Long term: 5.2 (3.6) vs. 5.1 (4.3); difference 0.10 (95% CI −1.36 to 1.56)

HADS Depression (0-21)

Baseline: 3.8 (1.27) vs. 4.1 (4.0)

Long term: 3.8 (3.6) vs. 4.0 (4.5): difference −0.20 (95% CI −1.70 to 1.30)

A vs. B, Mean (SD)

Number of health care visits for spinal pain during the past year

12 months before treatment: 2 vs. 1.5

Long term: 1.25 vs. 2.5, p=0.06

Smeets, 2006a, 2008

Netherlands

Pain duration: 56.7 months

RCT

Fair

A. Comprehensive pain management program (n=61): 10 weeks (79 hours total), low intensity, group and individual, outdoor rehabilitation centers

B. Psychological Therapy only (CBT) only (n=58): 10 weeks (26.5 hours total), low intensity, group and individual, rehabilitation center

Mean age: 42 years

Male: 53%

Race/ethnicity: NR

Pain etiology/type: Pain etiology/type: LBP

-

radiation of pain below knee: 49%

-

radiation of pain above knee: 37%

-

without radiation of pain: 14%

Disability:

Full sick leave/disability pension: 38%

Partial sick leave/disability pension: 24%

Comorbidities: NR

A vs. B, adjusted mean change score (SD) from baseline

VAS, current pain (0-10)

Baseline: 4.598 (2.395) vs. 4.884 (2.351)

Postintervention: −0.490 (–1.132 to 0.152) vs. −1.025 (–1.669 to – 0.381); adjusted difference in change scores 0.535 (95% CI −0.373 to 1.442)

Intermediate term: A 0.217 (–0.435 to 0.870) vs. – 0.408 (–1.056 to 0.241); adjusted difference in change scores 0.625 (95% CI −0.294 to 1.544)

Long term: 0.573 (–0.079 to 1.225) vs. −0.315 (–0.971 to 0.341); adjusted difference in change scores 0.888 (95% CI −0.036 to 1.813)

VAS, main (activity) complaints (0-10)

Baseline: 7.244 (1.703) vs. 7.471 (1.619)

Postintervention: −1.748 (–2.418 to −1.078) vs. −1.574 (–2.251 to – 0.898); adjusted difference in change scores −0.174 (95% CI −1.123 to 0.775)

Intermediate term: −1.285 (–1.962 to −0.608) vs. −1.767 (–2.444 to – 1.090); adjusted difference in changes scores 0.482 (95% CI −0.474 to 1.438)

Long term: −1.195 (–1.874 to – 0.515) vs. −2.019 (–2.705 vs. – 1.332); adjusted difference in change scores 0.824 (95% CI – 0.140 to 1.788)

MPQ Pain Rating Index Total score (PRI-T) (scale NR)

Baseline: 18.08 (9.04) 17.86 (9.94)

Postintervention: −1.45 (–4.10 to 1.19) vs. −3.52 (–6.22 to −0.82); adjusted difference in change scores 2.06 (95% CI −1.55 to 5.68) Intermediate term: −1.15 (–3.84 to 1.53) vs. −2.21 (–4.91 to 0.50); adjusted difference in change scores 1.05 (95% CI −2.60 to 4.71)

Long term: 0.94 (–1.74 to 3.63) vs. −1.84 (–4.60 to 0.91); adjusted difference in change scores 2.79 (95% CI −0.91 to 6.48)

RMDQ (0-23)

Baseline (mean, SD): 13.51 (3.92) vs. 13.74 (3.65)

Postintervention:–2.47 (–3.86 to – 1.25) vs. −3.04 (–4.29 to −1.79); adjusted difference in change scores 0.58 (95% CI −1.08 to 2.24) Intermediate term: −2.54 (–3.76 to – 1.31) vs. −3.65 (–4.90 to −2.40); adjusted difference in change scores 1.11 (95% CI −0.56 to 2.79)

Long term: −2.12 (–3.36 to −0.89) vs. −3.74 (–5.01 vs. −2.48); adjusted difference in change scores 1.62 (95% CI −0.06 to 3.31)

A vs. B, adjusted mean change (SD) from baseline

BDI (0-63)

Baseline: 9.75 (6.68) vs. 10.45 (7.06)

Postintervention: −0.69 (–2.09 to 0.71) vs. −2.31 (–3.72 to −0.91); adjusted difference in change scores 1.62 (95% CI −0.36 to 3.61)

Intermediate term: −2.14 (–3.57 to – 0.71) vs. −2.41 (–3.81 to −1.00); adjusted difference in change scores 0.26 (95% CI −1.74 to 2.27)

Long term: −2.17 (–3.60 to −0.75) vs. −2.08 (–3.52 to −0.65); adjusted difference in change scores −0.09 (95% CI −2.11 to 1.93)

Global Improvement (1-7)

Postintervention: 4.53 (4.13 to 4.93) vs. 4.71 (4.30 to 5.11); adjusted difference in change scores −0.18 (95% CI −0.73 to 0.37)

Intermediate term: 4.00 (3.60 to 4.40) vs. 4.76 (4.36 to 5.17); adjusted difference in change scores −0.76 (95% CI −1.31 to −0.21)

Long term: 3.89 (3.49 to 4.29) vs. 4.54 (4.13 to 4.95); adjusted difference in change scores −0.65 (95% CI −1.21 to −0.10)

A vs. B, % (n/N) or mean (SD)

Harms

-

Increased pain in the lower back or radiating leg pain leading to withdrawal from the trial: 5.5% (3/55) vs. 0% (0/55)

-

No other adverse events were reported in either group

VAS Satisfaction (0-100)

(effect modification by RDQ)

-

10th percentile of baseline RMDQ (=9)

Postintervention: 64.98 (25.30) vs. NR; adjusted difference for group B versus group A: −0.99 (95% CI −18.55 to 16.56)
-

50th percentile of baseline RMDQ (=14)

Postintervention: 70.24 (25.30) vs. NR; adjusted difference for group B versus group A: −0.89 (95% CI −13.16 to 11.28)
-

90th percentile of baseline RMDQ (=19)

Postintervention: 70.24 (25.30) vs. NR; adjusted difference for group B versus group A: −0.78 (95% CI −19.11 to 17.55)

Turner, 1990

USA

Duration of pain: 155 months

RCT

Poor

A. Comprehensive pain management program (n=18): 8 weeks (4 hours/week, 32 hours total), low intensity, Individual and group, Outpatient

B. Psychological Therapy alone (n=18): 8 weeks (2 hours/week, 16 hours total), low intensity, Individual and group, outpatient

Mean age: 44 years

Male: 52.1%

Race/ethnicity: White 100%

Pain etiology/type: Chronic LBP (≥6 months)

Disability: N/A

Comorbidities: NR

A vs. B, Mean (SD)

MPQ Pain Rating Index (0-78)

Baseline: 25.54 (12.41) vs. 20.96 (9.95)

Postintervention: 14.78 (11.44) vs. 17.71 (12.08)

Intermediate term: 13.29 (9.15) vs. 19.50 (15.72)

Long term: 18.21 (13.31) vs. 16.41 (13.63)

SIP (0-100)

Baseline: 8.50 (4.59) vs. 7.90 (6.43)

Postintervention: 3.63 (2.98) vs. 4.72 (4.12)

Intermediate term: 4.51 (4.68) vs. 7.60 (9.86)

Long term: 4.75 (3.40) vs. 5.25 (6.72)

A vs. B, Mean (SD)

CES-D (0-60)

Baseline: 12.38 (7.31) vs. 10.40 (7.51)

Postintervention: 7.36 (5.89) v vs. 8.08 (4.95)

Intermediate term: 8.29 (7.94) vs. 11.36 (8.30)

Long term: 10.00 (7.57) vs. 8.29 (7.74)

Patient satisfaction (1-7)

Postintervention: 5.50 (NR) vs. 4.00 (NR), p<0.05

A vs. B, Mean (SD)

Harms: NR

Patient satisfaction (1-7)

Postintervention: 5.50 (NR) vs. 4.00 (NR), p<0.05

Turner-Stokes, 2003

UK

Pain duration: 105.6 months

RCT

Poor

A. Comprehensive pain management program (73): 8 weeks (2 full afternoons per week, ~72 hours total), low intensity, group, Outpatient pain management clinics

B. Psychological Therapy alone (n=53): 8 weeks (1 hour every other week, 4 hours total), low intensity, group, outpatient

Mean age: 47 years

Male: 31%

Race/ethnicity: NR

Pain etiology/type: Chronic pain

Disability: NR

Comorbidities: NR

Mean difference (95% CI)

WHYMPI Pain Severity (0-6)

Baseline: adjusted difference −0.24 (95% CI −0.66 to 0.15), p=0.26

Postintervention: adjusted −0.07 (95% CI −0.50 to 0.35)

Intermediate term: adjusted difference −0.17 (95% CI −0.59 to 0.24)

WHYMPI Pain Interference subscale (0-6)

Baseline: adjusted difference −0.23 (95% CI −0.65 to 0.19)

Postintervention: adjusted −0.07 (95% CI −0.44 to 0.30)

Intermediate term: adjusted difference −0.28 (95% CI −0.69 to 0.13)

WHYMPI General Activities subscale (0-6)

Baseline: adjusted difference 0.22 (95% CI, −0.15 to 0.59)

Postintervention: adjusted difference −0.17 (95% CI −0.47 to 0.13)

Intermediate term: adjusted difference −0.11 (95% CI −0.44 to 0.21)

Mean difference (95% CI)

BDI (0-63)

Baseline: adjusted difference −1.12 (95% CI −4.43 to 2.41)

Postintervention: adjusted difference 0.91 (95% CI −1.89 to 3.71)

Intermediate term: adjusted difference −2.19 (95% CI −4.69 to 0.32)

STAI (20-80)

Baseline: adjusted difference 2.25 (95% CI −2.36 to 6.88)

Postintervention: adjusted difference −2.3 (95% CI −6.21 to 1.59), p=0.24

Intermediate term adjusted difference −3.43 (95% CI −7.81 to 0.94)

WHYMPI Control over Pain subscale (0-6)

Baseline: adjusted difference 0.46 (95% CI −0.04 to 0.97)

Postintervention: adjusted difference −0.15 (95% CI −0.59 to 0.29)

Intermediate term: adjusted difference 0.16 (95% CI −0.27 to 0.59)

NR

BDI = Beck Depression Inventory; CES-D = Center for Epidemiological Studies Depression; CI = confidence interval; HADS = Hospital Anxiety and Depression Scale; HRQOL = health-related quality of life; LBP = low back pain; MANCOVA = Multivariate analysis of covariance; MPQ = McGill Pain Questionnaire; NR = not reported; PDI = Pain Disability Index; RCT = randomized controlled trial; RMDQ = Roland Morris Disability Questionnaire; SF-36 = Short-form 36 questionnaire; SIP = Sickness Impact Profile; STAI = State-Trait Anxiety Inventory; SD = standard deviation; SF-36 = Short-Form 36 questionnaire; UK = United Kingdom; VAS = visual analog scale; WHYMPI = West Haven-Yale Multidimensional Pain Inventory.

Table B-10Summary results for trials addressing KQ2: IPMPs

Author, Year

Country

Pain Duration

Study Design

Study Quality

Intervention (n)

Comparator (n)

Duration/Intensity

Session Format

Setting

Population

Primary Outcomes:

Pain, Function, and Opioid Use

Secondary Outcomes:

HRQOL, Psychological Measures, Global Improvement

Harms

Utilization

Patient Satisfaction

Allen, 2017

USA

Mean duration of symptoms: 124.8 months

Cluster RCT

Fair

A. Patient focused multidisciplinary treatment + provider focused multidisciplinary treatment + usual care (n=140 patients, 5 providers): 12 months (time duration NR), individual, community–based outpatient clinics

B. Provider focused multidisciplinary treatment + usual care (n=140 patients, 5 providers): 12 months

C. Patient focused multidisciplinary treatment + usual care (n=128 patients, 5 providers): 12 months

Patient Participants

Mean age: 63.1 years

Male: 25%

Non-White race: 41%

Joints with OA:

-

Knee only: 85%

-

Hip only: 9%

-

Knee and hip: 6%

Disabled: 7%

Fair or poor health: 20%

Mean BMI: 35.6 kg/m2

Clinic and Provider Characteristics

Mean providers: 7.3

Mean medical physicians and osteopaths: 6.2

Mean nurse practitioners and physician assistants: 1.1

Family medicine practice: 60%

Internal medicine practice: 40%

Providers:

-

Male: 38%

-

Mean years since graduation: 18.9 years

Mean change from baseline (SD) (unless otherwise stated)

Estimated percentage improving ≥18% on WOMAC score from baseline (8.7-point reduction) a

A vs. B

Postintervention: 44% (95% CI 35% to 56%) vs. 35% (95% CI 28% to 44%)

A vs. C

Postintervention: 44% (95% CI 35% to 56%) vs. 49% (95% CI 37% to 63%)

B vs. C

Postintervention: 35% (95% CI 28% to 44%) vs. 49% (95% CI 37% to 63%)

WOMAC Total (0-96)

A vs. B

Baseline: 40.1 (15.8) vs. 37.7 (17.9)

Postintervention change: −6.8 (13.2) vs. −3.7 (13.4), difference in change scores −3.1 (95% CI −5.6 to 0.4)

A vs. C

Baseline: 40.1 (15.8) vs. 41.0 (15.9)

Postintervention change: −6.8 (13.2) vs. −7.7 (13.1), difference in change scores 0.90 (95% CI −2.8 to 4.7)

B vs. C

Baseline: 37.7 (17.9) vs. 41.0 (15.9)

Postintervention change: −3.7 (13.4) vs. −7.7 (13.1), difference in change scores 4.0 (95% CI 0.46 to 7.5)

WOMAC Pain (0-20)

A vs. B

Baseline: 8.4 (NR) vs. 8.0 (NR)

Postintervention change: −1.4 (3.6) vs. −0.8 (3.7), difference in change scores −0.6 (95% CI – 1.6 to −0.4) [on 0–10 scale, −0.3 (95% CI −0.8 to −0.2)]

A vs. C

Baseline: 8.4 (NR) vs. 8.8 (NR)

Postintervention change: −1.4 (3.6) vs. −1.5 (3.5), difference in change scores 0.10 (95% CI −0.9 to 1.1) [0–10 scale −0.05, 95%CI −0.45 to 0.55]

B vs. C

Baseline: 8.0 (NR) vs. 8.8 (NR)

Postintervention change: −0.8 (3.7) vs. −1.5 (3.5), difference in change scores 0.70 (95% CI – 0.27 to 1.7)

WOMAC Function (0-68)

A vs. B

Baseline: 27.5 (NR) vs. 26.0 (NR)

Postintervention change: −4.8 (9.3) vs. −2.3 (9.7), difference in change scores −2.5 (95% CI – 5.0 to 0.0)

A vs. C

Baseline: 27.5 (NR) vs. 28.5 (NR)

Postintervention change: −4.8 (9.3) vs. −5.6 (9.3), difference in change scores 0.80 (95% CI – 1.8 to 3.4)

B vs. C

Baseline: 26.0 (NR) vs. 28.5 (NR)

Postintervention change: −2.3 (9.7) vs. −5.6 (9.3), difference in change scores 3.3 (95% CI 0.8 to 5.8)

SPPB (Physical Function) (scale NR)

A vs. B

Baseline: 8.5 (NR) vs. 8.8 (NR)

Postintervention change: −0.3 (2.1) vs. −0.5 (2.0), difference in change scores 0.2 (95% CI – 0.4 to 0.7)

A vs. C

Baseline: 8.5 (NR) vs. 8.3 (NR)

Postintervention change: −0.3 (2.1) vs. −0.3 (2.0), difference in change scores 0.0 (95% CI – 0.6 to 0.6)

B vs. C

Baseline: 8.8 (NR) vs. 8.3 (NR)

Postintervention change: −0.5 (2.0) vs. −0.3 (2.0), difference in change scores −0.2 (95% CI – 0.7 to 0.3)

Mean change from baseline (SD)

PHQ-8 (0-24)

A vs. B

Baseline: 4.9 (NR) vs. 4.5 (NR)

Postintervention change: −0.6 (3.1) vs. 0 (3.1), difference in change scores −0.6 (95% CI −1.4 to 0.2)

A vs. C

Baseline: 4.9 (NR) vs. 4.8 (NR)

Postintervention change: −0.6 (3.1) vs. −0.4 (3.0), difference in change scores −0.2 (95% CI −1.1 to 0.7)

B vs. C

Baseline: 4.5 (NR) vs. 4.8 (NR)

Postintervention change: 0 (3.1) vs. −0.4 (3.0), difference in change scores 0.4 (95% CI −0.4 to 1.2)

% (n/N)

Harms

No study-related adverse events occurred

Self–reported OA treatments initiated during study period

A vs. B

New pain medication (type not specified: 38.8% (40/103) vs. 33.1% (41/124), RR 1.2 (95% CI 0.83 to 1.7)

Joint replacement surgery: 3.6% (5/139) vs. 2.1% (3/143), RR 1.7 (95% CI 0.42 to 7.0)

A vs. C

New pain medication (type not specified): 38.8% (40/103) vs. 27.8% (27/97), RR 1.4 (95% CI 0.93 to 2.1)

Joint replacement surgery: 3.6% (5/139) vs. 3.9% (5/128), RR 0.92 (95% CI 0.27 to 3.1)

B vs. C

New pain medication (type not specified): 33.1% (41/124) vs. 27.8% (27/97), RR 1.2 (95% CI 0.79 to 1.8)

Joint replacement surgery: 2.1% (3/143) vs. 3.9% (5/128), RR 0.54 (95% CI 0.13 to 2.2)

Calner, 2017

Sweden

Mean duration of pain: 79 months

RCT

Fair

A. Multidisciplinary rehab + web-based intervention (Web-BCPA) (n=60): minimum 1.5 months of 2–3 sessions/week; total duration 12 months (time duration NR), mode of delivery NR, Outpatient healthcare centers

B. Multidisciplinary rehab alone (n=49)

Mean age: 43 years

Male: 57%

Race/Ethnicity: NR

Disability: NR

-

Working: 28%

-

Unemployed: 7%

-

Temporarily

-

Unemployed: 4%

A vs. B, % (n/N) or mean (SD)

MCID (improvement) of ≥30% on VAS pain

Short term: 22% (11/48) vs. 23% (8/35); RR 1.00 (95% CI 0.45 to 2.23)

Long term (12 months): 28% (12/44) vs. 22% (8/36); RR 1.23 (95% CI 0.56 to 2.67)

VAS pain (0-10)

Baseline: 6.61 (1.67) vs. 6.47 (1.62)

Short term: 5.94 (2.14) vs. 5.49 (2.30); adjustedb treatment effect, 0.34 (95% CI −0.41 to 1.09)

Long term (12 months): 5.66 (2.07) vs. 5.73 (2.25); adjustedb treatment effect, −0.13 (95% CI −0.91 to 0.66)

MCID (improvement) of ≥30% on PDI

Short term: 20% (10/48) vs. 24% (8/35); RR 0.91 (95% CI 0.40 to 2.07)

Long term (12 months): 31% (14/44) vs. 30% (11/36); RR 1.04 (95% CI 0.54 to 2.01)

PDI (0-70)

Baseline: 36.9 (11.5) vs. 31.9 (13.5)

Short term: 33.0 (15.3) vs. 28.3 (15.1); adjustedb treatment effect, −0.4 (95% CI −5.8 to 5.1)

Long term (12 months): 30.8 (16.2) vs. 28.7 (17.1); adjustedb treatment effect, −2.6 (95% CI – 8.2 to 2.9)

A vs. B, % (n/N) or mean (SD)

MCID (improvement) of ≥30% on SF-36 subscales:

Physical function:

Short term: 31% (15/48) vs. 14% (5/35); RR 2.19 (95% CI 0.88 to 5.45)

Long term (12 months): 31% (14/44) vs. 14% (5/36); RR 2.29 (95% CI 0.91 to 5.76)

Role physical

Short term: 25% (12/48) vs. 29% (10/35); RR 0.88 (95% CI 0.43 to 1.79)

Long term (12 months): 29% (13/44) vs. 31% (11/36); RR 0.97 (95% CI 0.49 to 1.89)

Bodily pain

Short term: 52% (25/48) vs. 49% (17/35); RR 1.07 (95% CI 0.69 to 1.66)

Long term (12 months): 48% (21/44) vs. 40% (14/36); RR 1.23 (95% CI 0.73 to 2.05)

General health

Short term: 32% (15/48) vs. 26% (9/35); RR 1.22 (95% CI 0.60 to 2.45

Long term (12 months): 25% (11/44) vs. 31% (11/36); RR 0.82 (95% CI 0.40 to 1.66)

Vitality

Short term: 48% (23/48) vs. 37% (13/35); RR 1.29 (95% CI 0.77 to 2.17)

Long term (12 months): 46% (20/44) vs. 31% (11/36); RR 1.49 (95% CI 0.83 to 2.68)

Social functioning

Short term: 38% (18/48) vs. 49% (17/35); RR 0.77 (95% CI 0.47 to 1.27)

Long term (12 months): 33% (15/44) vs. 46% (17/36); RR 0.72 (95% CI 0.42 to 1.23)

Emotional role

Short term: 33% (16/48) vs. 29% (10/35); RR 1.17 (95% CI 0.60 to 2.26)

Long term (12 months): 25% (11/44) vs. 20% (7/36); RR 1.29 (95% CI 0.56 to 2.98)

Mental health

Short term: 17% (8/48) vs. 29% (10/35); RR 0.58 (95% CI 0.26 to 1.33)

Long term (12 months): 15% (7/44) vs. 26% (9/36); RR 0.64 (95% CI 0.26 to 1.54)

SF-36 (0-100) mean scores

Physical function

Baseline: 49.8 (22.5) vs. 60.1 (23.5)

Short term: 52.1 (24.5) vs. 65.9 (22.2); adjustedb treatment effect 0.8 (95% CI −4.7 to 6.2)

Long term (12 months): 52.2 (24.0) vs. 63.5 (25.1); adjustedb treatment effect 3.6 (95% CI −2.6 to 9.8)

Role physical

Baseline: 9.1 (23.3) vs. 11.4 (24.4)

Short term: 20.3 (32.1) vs. 25.7 (39.1); adjustedb treatment effect −2.6 (95% CI −16.4 to 11.2)

Long term (12 months): 23.9 (35.3) vs. 25.0 (32.2); adjustedb treatment effect – 0.9 (95% CI −15.0 to 16.7)

Bodily pain

Baseline: 24.8 (14.2) vs. 26.9 (13.9)

Short term: 32.2 (16.9) vs. 35.3 (19.0); adjustedb treatment effect −0.1 (95% CI −6.9 to 6.7)

Long term (12 months): 34.0 (15.6) vs. 32.7 (20.5); adjustedb treatment effect 4.8 (95% CI −1.8 to 11.3)

General health

Baseline: 40.4 (17.9) vs. 44.0 (17.0)

Short term: 46.5 (20.1) vs. 48.7 (21.3); adjustedb treatment effect 2.0 (95% CI −3.5 to 7.5)

Long term (12 months): 43.4 (19.5) vs. 45.4 (20.9); adjustedb treatment effect 2.4 (95% CI −4.9 to 9.6)

Vitality

Baseline: 24.6 (17.4) vs. 26.9 (18.5)

Short term: 34.3 (19.7) vs. 34.7 (25.1); adjustedb treatment effect 3.0 (95% CI −5.1 to 11.2)

Long term (12 months): 36.8 (21.1) vs. 32.1 (23.6); adjustedb treatment effect 8.1 (95% CI −0.6 to 16.9)

Social functioning

Baseline: 46.8 (24.1) vs. 51.1 (27.3)

Short term: 54.2 (24.9) vs. 67.5 (24.3); adjustedb treatment effect −8.9 (95% CI −18.6 to 0.8)

Long term (12 months): 59.9 (25.7) vs. 63.2 (27.5); adjustedb treatment effect −0.1 (95% CI −10.8 to 10.5)

Emotional role

Baseline: 47.9 (45.7) vs. 56.8 (41.7)

Short term: 63.2 (44.1) vs. 73.3 (36.9); adjustedb treatment effect −2.6 (95% CI −20.9 to 15.8)

Long term (12 months): 69.5 (16.0) vs. 65.7 (42.5); adjustedb treatment effect 3.9 (95% CI −16.4 to 24.3)

Mental health

Baseline: 59.1 (20.9) 62.0 (19.9)

Short term: 67.8 (16.4) vs. 70.4 (18.5); adjustedb treatment effect −2.0 (95% CI −8.8 to 4.8)

Long term (12 months): 69.4 (16.0) vs. 66.9 (18.9); adjustedb treatment effect 3.2 (95% CI −3.9 to 10.39)

NR

BCPA = behavior change programme for activity; BMI = Body mass index; CI = confidence interval; GHQ = General Health Questionnaire; HRQOL = Health-related quality of life; MCID = minimal clinically important difference; MPQ = McGill Pain Questionnaire; NR = not reported; OA = osteoarthritis; PDI = Pain Disability Index; PHQ–8 = Patient Health Questionnaire–8; RCT = randomized controlled trial; RR = risk ratio; SF-12 = Short-Form 12; SF-36 = Short-Form 36 questionnaire; SPPB = Short Physical Performance battery; USA = United States of America; VAS = visual analog scale; WOMAC = Western Ontario and McMaster Universities Osteoarthritis Index

a

Data calculated by hierarchical linear mixed models and based on author imputation

b

Linear mixed model was adjusted for sex and interaction between time and group

Table B-11Summary results for trials addressing KQ2: CPMPs

Author, Year

Country

Pain Duration

Study Design

Study Quality

Comparison

Intervention (n)

Comparator (n)

Duration/Intensity Session Format Setting

Population

Primary Outcomes:

Pain, Function, and Opioid Use

Secondary Outcomes:

HRQOL, Psychological Measures, Global Improvement

Harms

Utilization

Patient Satisfaction

Bendix 1995, 1997, 1998a, 1998b (PROJECT B)

Denmark

Duration of pain: ≥6 months (NOS)

RCT

Fair

Higher vs. Lower Total Program Hours

A. CPMP – 135 hours (n=46)

3 weeks full time, 39 hours/week + 1 day (6 hours) weekly for 3 (135 hours total), group, outpatient rheumatology clinic

B. CPMP – 24 hours (n=43)

6 weeks, 4 hours/week (24 hours total), group, outpatient rheumatology clinic

Mean age: 42 years

% Male: 25%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

Disability: 68% (working incapable)

Comorbidities:

Smoker: 64%

Prior back surgery: 16%

A vs. B median (IQR)

VAS back pain (0-10)

Baseline: 5.3 (NR) vs. 5.9 (NR)

Short term: 2.7 (1.4 to 4.3) vs. 5.6 (3.8 to 7.6), p≤0.001

Long term (12 months): 3.3 (2.1 to 5.6) vs. 6.5 (4.8 to 7.7), p≤0.001

Long term (24 months): 3 (2 to 6) vs. 6 (4 to 8), p≤0.001

Long term (60 months): 4 (NR) vs. 6 (NR), p≤0.001

VAS leg pain (0-10)

Baseline: 2.9 (NR) vs. 3.7 (NR)

Short term: 0.4 (0 to 2.3) vs. 3.1 (0.5 to 5.9), p=0.01

Long term (12 months): 2.1 (0.2 to 4.13) vs. 4.8 (2.3 to 7.3) p=0.001

Long term (24 months): 2 (0 to 5) vs. 5 (1 to 6), p=0.003

Long term (60 months): 3 (NR) vs. 4 (NR), p=NS

Patient subjective disability due to back pain (0-30)

Baseline: 15.5 (NR) vs. 15.3 (NR)

Short term: 8.5 (5 to 15) vs. 16.1 (11 to 19), p=0.002

Long term (12 months): 8.9 (5 to 13) vs. 16.4 (14 to 19), p<0.001

Long term (24 months): 10 (6 to 14) vs. 17 (9 to 21), p=0.002

Long term (60 months): 8 (NR) vs. 16 (NR), p=0.03

A vs. B, median (IQR)

Global improvement (1-5)

Long term (24 months): 2 (1 to 3) vs. 3 (2 to 3), p=0.003

Long term (60 months): 2 (NR) vs. 3 (NR), p=0.003

A vs. B, % (n/N)

Harms: NR

Proportion of patients hospitalized due to low back pain

Long term (60 months): 22% (8/37) vs. 23% (7/31); RR 0.96 (95% CI 0.39 to 2.34)

Proportion of patients who underwent back surgery during the study period, % (

Long term (60 months): 5% (2/37) vs. 10% (3/31); RR 0.56 (95% CI 0.10 to 3.13)

Proportion of patients taking prescription pain medications (opioids not specified), % (n/N)

Baseline: 75% (30/40) vs. 66% (23/35)

Long term (24 months): 50% (20/40) vs. 67% (23/34); RR 0.74 (95% CI 0.50 to 1.09)

Rose 1997 (Part 2)a

UK

Mean duration of pain: 97 months

RCT

Poor

Higher vs. Lower Total Program Hours

A. CPMP – 60 hours: 10 consecutive workdays, 60 hours total, group, outpatient

B. CPMP – 30 hours: 5 consecutive full days, 30 hours total, group, outpatient

C. CPMP – 15 hours: 5 consecutive half days, 15 hours total, group, outpatient

Mean age: 42 years

% Male: 41%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP and/or referred leg pain

Disability or sickness benefit: 64% (completers only)

Comorbidities: NR

Prior spinal surgery: 13%

Mean (SDs NR)

VAS pain (0-10)

A vs. B

Baseline: 5.0 vs. 6.0

Postintervention: 5.0 vs. 4.3

Intermediate term: 5.1 vs. 5.2

p=ns for all comparisons

A vs. C

Baseline: 5.0 vs. 5.3

Postintervention: 5.0 vs. 4.9

Intermediate term: 5.1 vs. 4.3

p=ns for all comparisons

RMDQ (0-24)

A vs. B

Baseline: 10.7 vs. 14.0

Postintervention: 8.4 vs. 9.9

Intermediate term: 9.5 vs. 11.5

p=ns for all comparisons

A vs. C

Baseline: 10.7 vs. 10.8

Postintervention: 8.4 vs. 8.8

Intermediate term: 9.5 vs. 10.0

p=ns for all comparisons

Mean (SDs NR)

The Modified Zung Depression Inventory (Scale NR)

A vs. B

Baseline: 25.0 vs. 26.0

Postintervention: 22.0 vs. 21.0

Intermediate term: 21.1 vs. 22.0

p=ns for all comparisons

A vs. C

Baseline: 25.0 vs. 24.0

Postintervention: 22.0 vs. 21.1

Intermediate term: 21.1 vs. 21.1

p=ns for all comparisons

NR

Saral 2016

Turkey

Mean duration of pain 90 months

RCT

Fair

Higher vs. Lower Total Program Hours

A. CPMP – 75 hours (n=22)

10 weeks, ~75 hours total, group, outpatient

B. CPMP – 10 hours (n=22)

2 days, ~10 hours total, group, outpatient

Mean age: 40 years

% Female: 100%

Race/ethnicity: NR

Pain etiology/type: Fibromyalgia

Disability: NR

Comorbidities: NR

-

Excluded: advanced psychiatric diseases and serious physical comorbidities

A vs. B, Mean (SD)

VAS pain (0 to 10)

Baseline: 8.2 (0.9) vs. 7.6 (0.8)

Intermediate term: 5.1 (2.4) vs. 5.8 (1.0), difference −0.70 (95% CI – 1.82 to 0.42)

FIQ (0-100)

Baseline: 71.6 (14.2) vs. 67.7 (12.0)

Intermediate term: 53.9 (19.3) vs. 54.5 (14.2), difference −0.03 (95% CI −0.66 to 0.59)

A vs. B, Mean (SD)

SF-36 PCS (0-100)

Baseline: 32.8 (7.9) vs. 36.5 (8.7)

Intermediate term: 39.9 (7.5) vs. 39.6 (8.1), difference 0.30 (95% CI −4.69 to 5.29)

SF-36 MCS (0-100)

Baseline: 30.4 (11.7) vs. 33.2 (8.9)

Intermediate term: 40.7 (12.3) vs. 40.2 (10.0), difference 0.50 (95% CI −6.72 to 7.72)

BDI (0-63)

Baseline: 23.4 (11.0) vs. 20.7 (6.6)

Intermediate term: 16.6 (9.6) vs. 15.0 (10.2) , difference 0.16 (95% CI −0.46 to 0.78)

Harms: None reported; occasional mild increases in pain after some exercise sessions in both groups A and B.

Reneman, 2020

The Netherlands

Mean duration of pain: NR (>1 year = 74%)

RCT

Fair

Higher vs. Lower Total Program Hours

A. CPMP – Higher hours (n=81)

Intended duration: 12, 16 or 20 weeks (4 weeks/10 contact hours more than Group B)

Actual duration: 12 or 16 weeks: 96.3% (78/81)

Mean (SD) number of weeks of treatment: 11.7 (4.5)

Mean (SD) number of contact hours with providers: 30.7 (11.3)

Outpatient, Individual

B. CPMP – Lower hours (n=72)

Intended duration: 8, 12 or 16 weeks (4 weeks/10 contact hours less than Group A)

8 or 12 weeks: 98.6% (71/72)

Mean (SD) number of weeks of treatment: 10.8 (3.9)

Mean (SD) number of contact hours with providers: 29.8 (10.4)

Outpatient, Individual

Mean age: 44 years

% Male: 53%

Race/ethnicity: NR

Pain etiology/type: Chronic MSK pain

Disability:

-

Partial sick leave/disability pension: 37%

-

Full sick leave/disability pension: 13%

Other characteristics:
-

Excluded: comorbidities such as heart failure, rheumatoid arthritis, or psychiatric disorders preventing participation.

A vs. B, Mean (SD)

EQ5D VAS pain (0-10)

Baseline: 5.45 (1.78) vs. 5.44 (1.77)

Post-treatment: 6.75 (1.61) vs. 6.76 (1.87), difference −0.01 (95% CI – 0.697 to 0.677)

PDI (0-70)

Baseline: 36.1 (12.5) vs. 37.9 (14.2)

Post-treatment: 25.1 (15.0) vs. 26.6 (17.7), difference −1.5 (95% CI – 7.44 to 4.44)

EQ5D Index (0-1)

Baseline: 0.56 (0.19) vs. 0.54 (0.21)

Post-treatment: 0.70 (0.17) vs. 0.70 (0.20), difference 0.00 (95 % CI – 0.073 to 0.073)

Harms: No trial-related adverse events were reported.

Harkapaa, 1989, 1990

Finland

Mean duration of pain: 173 months

RCT

Poor

Inpatient vs. Outpatient Setting

A. CPMP - Inpatient (n=156)

2x/week for 2 months (15 sessions) + 2-week refresher sessions after 1.5 years, group, inpatient

B. CPMP - Outpatient (n=150)

2x/week for 2 months (15 sessions) + 8 refresher sessions after 1.5 years, group, outpatient

Mean age: 45 years

% Male: 62%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

-

Continuous LBP past year: 41%

-

Severe LBP past year: 84%

Disability: NR

Comorbidities: NR

Other characteristics:

-

Mean number of days of absenteeism due to LBP in past 2 years: 36

-

Use of analgesics (opioids NR): 63%

A vs. B, Mean (SD)b

Pain Index (0-400)

Baseline (mean, SD): 184.9 (76.9) vs. 178.6 (81.8) [4.6 (1.9) vs. 4.5 (2.0) on a 0-10 scale]

Short term: 128 (NR) vs. 146 (NR) [3.2 (1.3) vs. 3.6 (1.8) on a 0-10 scale]

Intermediate term: 158 (NR vs. 160 (NR) [3.9 (NR) vs. 4.0 (NR) on a 0-10 scale]

Long term (18 months): 156.5 (NR) vs. 174 (NR) [3.9 (1.6) vs. 4.3 (2.2) on a 0-10 scale]

Long term (22 months): 149 (NR) vs. 164 (NR) [3.7 (NR) vs. 4.1 (NR) on a 0-10 scale]

Long term (30 months): 161.5 (NR) vs. 168 (NR) [4.0 (1.7) vs. 4.2 (2.1) on a 0-10 scale]

LBP Disability Index (0-45)

Baseline (mean SD): 16.7 (7.9) vs. 17.6 (7.4)

Short term: 13.6 (9.7) vs. 14.7 (7.7)

Intermediate term: 15.7 (NR) vs. 16 (NR)

Long term (18 months): 15.6 (11.1) vs. 17.1 (9.0)

Long term (22 months): 14.5 (NR) vs. 15.65 (NR)

Long term (30 months): 15.4 (11.0) vs. 16.55 (8.7)

NRNR

Peters, 1990, 1992

New Zealand

Mean duration of pain: NR (6 to 48 months, 49%; 48 to ≥240 months, 51%)

RCT

Poor

Inpatient vs. Outpatient Setting

A. CPMP – Inpatient Setting (n=23)

4 weeks, intensity NR, group, inpatient

B. CPMP – Outpatient Setting (n=29)

9 weeks, 2 hours/week (18 hours total), outpatient

Mean age: 44 years

% Male: 38%

Race/Ethnicity:

-

European: 92%

-

Maori: 6%

-

Polynesian: 2%

Pain etiology/type (patient could have ≥1 pain type):
-

Back pain: 44%

-

Head pain: 31%

-

Arm pain: 27%

-

Leg pain: 19%

-

Chest pain: 13%

-

Abdomen pain: 8%

Disability: NR

Comorbidities: NR

-

Excluded: Psychotic illness

Mean (SD) or % (n/N)

Proportion of patients demonstrating treatment success (using medication appropriately + active + no pain increase), % (n/N)

Long term (mean 12 months)c: 68% (15/22) vs. 61% (11/18), RR 1.12 (95% CI 0.70 to 1.78)

VAS pain (0-10)

Baseline: 5.12 (2.56) vs. 5.25 (2.46)

Postintervention: 3.92 (2.33) vs. 4.25 (2.18), difference −0.33 (95% CI −1.80 to 1.14)

MPQ (scale NR)

Data NR – “mean scores indicate Group A’s scores reflect a trend towards greater reduction of pain intensity, in comparison with Group B”

SIP (scale NR)

Baseline: 204.31 (75.43) vs. 137.78 (105.49)

Postintervention: 122.89 (80.84) vs. 96.00 (77.84), difference 26.89 (95% CI −22.39 to 76.17)

Proportion of patients taking an opioid, % (n/N)

Baseline:

Any opioid: 31.8% (7/22) vs. 33% (6/18), RR 0.95 (95% CI 0.39 to 2.34)

-

strong opioid: 9.1% (2/22) vs. 17% (3/18), RR 0.55 (95% CI 0.10 to 2.92)

-

mild opioid: 22.7% (5/22) vs. 17% (3/18), RR 1.36 (95% CI 0.38 to 4.95)

Long term (mean 12 months): Any opioid: 13.6% (3/22) vs. 22% (4/18), RR 0.61 (95% CI 0.16 to 2.39)
-

strong opioid: 0% (0/22) vs. 6% (1/18), RR NC

-

mild opioid: 13.6% (3/22) vs. 17% (3/18), 0.82 (95% CI 0.19 to 3.57)

Mean (SD)

BDI

Baseline: 19.18 (9.34) vs. 13.55 (6.03)

Postintervention: 12.25 (15.64) vs. 10.73 (6.16), difference 1.52 (95% CI −5.59 to 8.63)

General Health Questionnaire

Baseline: 15.52 (8.58) vs. 8.67 (7.23)

Postintervention: 5.96 (7.11) vs. 5.91 (6.42), difference 0.05 (95% CI −4.09 to 4.19)

NR

Ronzi, 2017

France

Mean duration of pain: NR (>5 years: 60%)

RCT

Poor

Inpatient vs. Outpatient Setting

A. CPMP – Inpatient setting (n=49)

5 weeks, 30 hours/week (150 hours total), combo, inpatient

B. CPMP – Outpatient setting (n=56)

5 weeks, 11 hours/week (55 hours total), combo, outpatient

Median age: 40 years

% Male: 59%

Race/ethnicity: NR

Pain etiology/type: Chronic LBP (≥3 months)

Disability: NR

Sick leave: “almost all patients on sick leave”; median days in past year: 233

Comorbidities:

-

history of depression: <33%

Prior spine surgery: <33%

A vs. B

VAS pain (0-10)

Baseline (median, IQR): 5.4 (4.5 to 6.5) vs. 5.5 (3.6 to 6.8)

Long term (mean, SD): 4.5 (2.5) vs. 3.7 (3.4), difference 0.80 (95% CI – 0.48 to 2.08)

DPQ daily activity (%; lower = lower impact of pain on QOL)

Baseline (median, IQR): 63.0% (51.0% to 72.0%) vs. 57.0% (48.0% to 66.0%)

Long term (mean, SD): 51.0% (38.9%) vs. 39.0% (24.5%); difference 0.36% (95% CI −0.06% to 0.79%)

A vs. B, Median (IQR)

SF-36 PCS (0-100)

Baseline: 35.7 (29.4 to 39.5) vs. 34.5 (30.7 to 39.2)

Long term: 39.1 (33.8 to 50.4) vs. 41.6 (34.2 to 49.9)

p=NS for all

SF-36 MCS (0-100)

Baseline: 43.3 (32.1 to 49.8) vs. 43.4 (35.9 to 51.1)

Long term: 48.3 (42.1 to 53.4) vs. 46.6 (38.7 to 56.6)

p=NS for all

HADS (0-100)

Baseline: 17.0 (12.0 to 21.0) vs. 14.0 (11.0 to 18.0)

Long term: 11.5 (7.5 to 18.0) vs. 12.0 (7.0 to 15.0)

p=NS for all

DPQ anxiety and depression (%; lower = lower impact of pain on QOL)

Baseline: 45.0% (20.0% to 60.0%) vs. 35.0% (25.0% to 45.0%)

Long term: 30.0% (5.0% to 45.0%) vs. 25.0% (5.0% to 45.0%)

p=NS for all

Harms: None reported

Williams, 1996

UK

Mean duration of pain: 94 months

RCT

Poor

Inpatient vs. Outpatient Setting

A. CPMP – Inpatient setting (n=43)

4 weeks, 4.5 days/week (~144 hours total), group, inpatient

B. CPMP – Outpatient setting (n=45)

8 weeks, 3.5 hours/week (28 hours total), group, outpatient

Mean age: 50 years

% Male: 49%

Race/ethnicity: white, ~85%

Pain etiology/type:

-

back/neck/legs: 76%

-

central/peripheral nerve system damage: 25%

-

other tissue damage: 13%

-

unknown mechanism: 61%

Disability: 60%

Opioid use: 65%

Excess drug use: 58%

≥1 prior surgery: 40%

A vs. B, mean (SD)

VAS pain intensity (0-10)

Baseline: 7.11 (1.90) vs. 6.86 (1.49)

Short term: 6.00 (2.17) vs. 6.34 (1.96), difference −0.34 (95% CI −1.65 to 0.67)

Long term (12 months): 6.52 (2.11) vs. 7.46 (1.88), difference −0.94 (95% CI −19.5 to 0.07)

SIP (0-100)

Baseline: 29.53 (12.55) vs. 28.48 (9.49)

Short term: 15.81 (11.20) vs. 20.95 (10.29), difference −5.14 (95% CI – 10.41 to 0.13)

Long term (12 months): 19.40 (13.05) vs. 20.84 (9.58), difference −0.12 (95% CI −0.63 to 0.38)

Proportion of patients not using opioids, % (n/N)

Baseline: 47% (18/38) vs. 33% (11/33), RR 1.4 (95% CI 0.79 to 2.56)

Short term: 82% (31/38) vs. 57% (19/33), RR 1.42 (95% CI 1.02 to 1.97)

Long term (12 months): 63% (24/38) vs. 52% (17/33), RR 1.23 (95% CI 0.81 to 1.85)

Proportion of patients taking an opioid dose equivalent to >10 mg morphine per day

Baseline: 34.2% (13/38) vs. 48.5% (16/33), RR 0.71 (95% CI 0.40 to 1.24)

Short term: 10.5% (4/38) vs. 33.3% (11/33), RR 0.32 (95% CI 0.11 to 0.90)

Long term (12 months): 10.5% (4/38) vs.18.2% (6/33), RR 0.58 (95% CI 0.18 to 1.88)

Mean opioid dose per day (mg morphine equivalents)

Baseline: 30 mg vs. 22 mg

Short term: NR

Long term (12 months): 22 mg vs.15 mg, p=NS

A vs. B, mean (SD)

BDI (0-63)

Baseline: 17.8 (8.0) vs. 16.8 (5.6)

Short term: 9.5 (7.8) vs. 12.2 (6.3), difference −2.70 (95% CI −6.20 to 0.80)

Long term (12 months): 10.8 (8.9) vs. 14.7 (6.6), difference −3.90 (95% CI −7.79 to 0.172)

STAI (20-80)

Baseline: 45.1 (10.7) vs. 45.7 (8.2)

Short term: 36.8 (13.6) vs. 42.3 (10.6), difference −5.50 (95% CI – 11.53 to 0.53)

Long term (12 months):: NR

VAS pain distress (0-10)

Baseline: 6.64 (2.24) vs. 7.03 (2.10)

Short term: 4.16 (2.90) vs. 5.42 (2.75), difference −1.26 (95% CI −2.64 to 0.12)

Long term (12 months): 4.57 (2.94) vs. 7.37 (2.27), difference −2.80 (95% CI −4.16 to −1.44)

A vs. B

Harms: NR

Subsequent treatments

-

Surgery: 0% vs. 0%

-

Pain-relieving procedures (acupuncture, TENS, nerve blocks): 10.3% (3/29) vs. 60.7% (17/28), RR 0.17 (95% CI 0.06 to 0.52)

Rose 1997 (Part 1)a

UK

Mean duration of pain 97 months

RCT

Poor

Group vs. Individual Session Format

A. CPMP – Group format (n=26)

Duration and intensity NR, group, outpatient

B. CPMP – Individual format (n=24)

Duration and intensity NR, individual, outpatient

Mean age: 42 years

% Male: 41%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP (and/or referred leg pain)

Disability or sickness benefit: 64% (completers only)

Comorbidities: NR

Prior spinal surgery: 13%

Unsuccessful PT: 91%

A vs. B, Mean (SDs NR)d

VAS-pain

Baseline: 6.6 vs. 6.0

Postintervention: 5.8 vs. 4.7

Intermediate term: 6.5 vs. 6.0

p=NS for all

RDQ (0-24)

Baseline: 15.8 vs. 17.0

Postintervention: 13.3 vs. 11.1

Intermediate term: 13.3 vs. 11.1

p=NS for all

A vs. B, Mean (SDs NR)

The Modified Zung Depression Inventory (scale NR)

Baseline: 33.1 vs. 32.0

Postintervention: 27.0 vs. 27.0

Intermediate term: 28.0 vs. 26.1

p=NS for all

NR

Abbasi 2012

Iran

Mean duration of pain: 74 months

RCT

Poor

CPMP + additional components vs. standard CPMP

A. CPMP – Spouse-assisted (n=9)

7 weeks, 2 hours/week (14 hours total), combo (primarily group, individual if needed), outpatient

B. CPMP – Conventional, patient-oriented (n=10)

7 weeks, 2 hours/week (14 hours total), combo (primarily group, individual if needed), outpatient

Mean age: 45 years

% Male: 12%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

Disability: NR

Comorbidities:

-

Excluded: major cognitive dysfunction or coexisting psychiatric morbidity

A vs. B, Mean (SD)

VAS pain in last week (0-10)

Baseline: 5 (2.7) vs. 4.6 (2)

Postintervention: 3 (1.8) vs. 2.6 (2), difference 0.40 (95% CI −1.45 to 2.25)

Long term: 2.8 (2.7) vs. 3.7 (2.5), difference −0.90 (95% CI −3.42 to 1.62)

RDQ (0-24)

Baseline: 11.2 (4.3) vs. 12.1 (5.7)

Postintervention: 5.8 (3) vs. 6.2 (4.4), difference −0.40 (95% CI −4.10 to 3.30)

Long term: 8.2 (5.4) vs. 8.8 (5.9), difference −0.60 (95% CI −6.01 to 4.90)

NRNR

Altmaier 1992

US

Mean duration of pain: NR

RCT

Fair

CPMP + additional components vs. standard CPMP

A. CPMP + additional psychological components (n=24)

3 weeks, duration NR, intensity NR, inpatient

B. Standard CPMP (n=21)

3 weeks, duration NR, intensity NR, inpatient

Mean age: 40

% Male: 27%

Race/Ethnicity: NR

Mean duration of pain: NR

Pain etiology/type: Chronic LBP

Disability: 100% (inclusion criteria: disabled and not working due to pain for ≥3 to ≤30 months)

Comorbidities: NR

-

Excluded: “significant levels of depression or anger”

A vs. B, Mean (SD)

MPQ Present Pain Intensity (1-5)

Baseline: 2.24 (0.77) vs. 2.52 (0.81)

Postintervention: 2.05 (0.74) vs. 2.00 (0.89), difference 0.05 (95% CI −0.46 to 0.56)

Intermediate term: 2.33 (0.80) vs. 2.00 (0.95), difference 0.33 (95% CI −0.22 to 0.88)

MPQ Pain Rating Index (0-78)

Baseline: 22.00 (10.41) vs. 17.81 (9.06)

Postintervention: 21.71 (9.16) vs. 16.05 (9.31), difference 5.66 (95% CI −0.10 to 11.42)

Intermediate term: 20.33 (11.91) vs. 16.19 (12.48), difference 4.14 (95% CI −3.47 to 11.75)

WHYMPI Pain Interference Subscale (scale NR)

Baseline: 65.38 (13.23) vs. 65.10 (17.10)

Postintervention: 57.33 (15.06) vs. 57.67 (16.37), difference −0.34 (95% CI −10.2 to 9.47)

Intermediate term: 52.19 (19.58) vs. 50.71 (25.95), difference 1.48 (95% CI −12.86 to 15.82)

Low Back Pain Rating Scale Total Score (scale 0-130)

Baseline: 57.00 (9.89) vs. 60.19 (14.03)

Postintervention: 67.05 (11.01) vs. 71.19 (9.92), difference −4.14 (95% CI −10.68 to 2.39)

Intermediate term: 64.86 (12.56) vs. 70.76 (15.70), difference −5.90 (95% CI −14.77 to 2.97)

A vs. B, Mean (SD)

WHYMPI Negative Mood Subscale (scale NR)

Baseline: 17.24 (6.68) vs. 17.05 (6.72)

Postintervention: 14.19 (5.61) vs. 14.00 (5.92), difference 0.19 (95% CI −3.41 to 3.79)

Intermediate term: 16.24 (4.22) vs. 15.00 (6.15), difference 1.24 (95% CI −2.05 to 4.53)

NR

Van der Maas 2015

The Netherlands

Mean duration of pain: NR (≥2 years: 75%)

RCT

Fair

CPMP + additional components vs. standard CPMP

A. CPMP + Psychomotor Therapy (n=49)

3 days a week for 12 weeks, 104 hours total, group, outpatient

B. Standard CPMP (n=45)

3 days a week for 12 weeks, 94 hours total, group, outpatient

Mean age: 42 years

% Male: 14%

Race/ethnicity: NR

Pain etiology/type: Chronic MSK pain (≥3 months)

Disability: NR

Comorbidities: NR

-

Excluded: psychiatric diagnosis which could interfere with treatment

A vs. B, Mean (SD)e

PDI disability (0-70)

Baseline: 40.00 (8) vs. 40.34 (11)

Postintervention: 33.26 (7) vs. 36.63 (11), difference −3.37 (95% CI −7.12 to 0.38)

Short term: 31.33 (11) vs. 35.46 (12), difference −4.13 (95% CI −8.84 to 0.58)

Intermediate term: 31.82 (12) vs. 33.71 (14), difference −1.89 (95% CI −7.22 to 3.44)

Long term: 32.10 (12) vs. 32.40 (15), difference −0.30 (95% CI – 5.84 to 5.24)

A vs. B, Mean (SD)

RAND-36 physical component (0-100)

Baseline: 32.42 (7) vs. 31.51 (7)

Postintervention: 34.83 (8) vs. 32.62 (9), difference 2.21 (95% CI – 1.27 to 5.69)

Short term: 36.86 (8) vs. 34.36 (9), difference 2.50 (95% CI −0.98 to 5.98)

Intermediate term: 35.82 (8) vs. 32.17 (9), difference 3.65 (95% CI – 0.04 to 7.34)

Long term: 36.99 (7) vs. 33.90 (7), difference 3.09 (95% CI 0.22 to 5.96)

RAND-36 mental component (0-100)

Baseline: 39.89 (10) vs. 39.59 (11)

Postintervention: 43.45 (11) vs. 39.90 (12)

Short term: 42.33 (11) vs. 39.84 (10), difference 2.49 (95% CI −1.83 to 6.81)

Intermediate term: 45.59 (10) vs. 45.03 (10), difference 0.56 (95% CI −3.54 to 4.66)

Long term: 43.60 (11) vs. 44.59 (9), difference −0.99 (95% CI −5.13 to 3.15)

BDI (0-63)

Baseline: 20.23 (8) vs. 18.68 (4)

Postintervention: 12.81 (8) vs. 15.92 (9), difference −3.11 (95% CI −6.59 to 0.37)

Short term: 12.72 (6) vs. 15.33 (10), difference −2.61 (95% CI −5.96 to 0.74)

Intermediate term: 13.11 (8) vs. 13.76 (9), difference −0.65 (95% CI −4.13 to 2.83)

Long term: 13.32 (8) vs. 13.56 (9), difference −0.24 (95% CI −3.72 to 3.24)

NR

Kool, 2005, 2007

Switzerland

Mean duration of pain: NR (“nonacute”)

RCT

Fair

Different philosophical approaches to CPMP

A. CPMP - Function-Centered (n=87)

3 weeks, 6 days/week (24 hours/week, 72 hours total), individual inpatient

B. CPMP - Pain-Centered (n=87)

3 weeks, 6 days/week (15 hours/week, 45 hours total), individual, inpatient

Mean age: 42 years

% Male: 79%

Race/Ethnicity: NR

Pain etiology/type:

-

Nonacute LBP and leg pain: 83%

-

Nonacute LBP: 17%

Disability: NR

Comorbidities: NR

Other characteristics:

-

Mean days of sick leave prior 2 years before treatment: 192

-

Taking pain medication (opioids NR): 74%

A vs. B, mean difference (95%) in change scores from baseline

Pain NRS (0-10)

Baseline (mean, SD): 5.5 (2.0) vs. 5.7 (2.2)

Postintervention: difference in change scores −0.80 (–1.40 to −0.20)

Short term: difference in change scores −0.54 (–1.35 to 0.27)

PACT (0-200)

Baseline (mean, SD): 110 (39) vs. 102 (42)

Postintervention: difference in change scores −13.30 (–20.32 to – 6.28)

A vs. B, Mean (SD)

Global improvement (7-point Likert scale)

Postintervention: 4.4 (2.0) vs. 3.6 (2.0), difference 0.80 (95% CI 0.19 to 1.40)

Short term: no difference between groups (data NR)

A vs. B, Mean (SD)

Harms: NR

Patient satisfaction with treatment, median (IQR)

Long term (12 months): 6 (4 to 7) vs. 6 (4 to 7)

Leeuw, 2008

The Netherlands

Mean duration of pain: 108 months

RCT

Fair

Different philosophical approaches to CPMP

A. CPMP - “Exposure in vivo” (n=42)

8 weeks (2 hours/week, 16 hours total), individual, outpatient

B. CPMP - graded activity (n=43)

13 weeks (2 hours/week, 26 hours total), individual, outpatient

Mean age: 45 years

% Male: 52%

Race/Ethnicity: NR

Pain etiology/type: Chronic LBP

-

pain radiating to legs: 98%

Disability:
-

In receipt of a disability pension: 26%

-

Sick leave: 28%

Comorbidities: NR

Other characteristics:

-

Use of medication (opioids NR): 72%

-

Previous back surgery: 31%

-

Excluded: substance abuse, medical disorders or cardiovascular disease preventing physical exercise, serious psychopathology

A vs. B, mean (SD) or mean (95% CI) change from baseline

MPQ (0-100)

Baseline: 52.54 (12.77) vs. 54.66 (11.88)

Postintervention: 43.72 (21.24) vs. 44.07 (22.86), difference −0.35 (95% CI −10.37 to 9.67)

Intermediate term: 41.15 (22.26) vs. 40.45 (22.25), difference 0.70 (95% CI −9.70 to 11.10)

Quebec Back Pain Disability Scale (0-100)

Baseline: 53.61 (11.63) vs. 51.88 (13.54)

Postintervention: 35.90 (20.45) vs. 41.69 (22.58), difference −5.79 (95% CI −15.56 to 3.98)

Intermediate term: 39.00 (20.93) vs. 41.94 (19.29), difference −2.94 (95% CI −12.36 to 6.48)

Proportion of patients reporting clinically relevant changes on the RMDQ

Postintervention: 54% (22/41) vs. 42% (15/36), RR 1.29 (95% CI 0.80 to 2.08)

Intermediate term: 50% (19/38) vs. 34% (12/35), RR 1.46 (0.83 to 2.55)

RMDQ (0-24)

Baseline: 15.23 (3.64) vs. 14.27 (3.44)

Postintervention: difference in change scores from baseline −1.95 (95% CI −4.61 to 0.71)

Intermediate term: difference in change scores from baseline −2.11 (95% CI −4.76 to 0.54)

NRAdverse events/harms: - Deterioration during intervention (i.e., treatment counterproductive): 0% (0/42) vs. 2% (1/43)
-

No other adverse events or side effects related to the interventions were reported

Rothman 2013

Sweden

Median duration of pain: 18 months

RCT

Fair

CPMP with vs. without pretreatment assessment

A. CPMP with “multimodal” pretreatment assessment (n=99)

Duration NR, Intensity NR, combo, outpatient

B. CPMP using standard process (n=108)

Duration NR, Intensity NR, combo, outpatient

Median age (IQR): Treatment: 40 (32 to 47) years, Control: 40 (33-48) years

% Male: 23.6%

Race/ethnicity: NR

Pain etiology/type: Chronic muscular pain

Disability: NR

Comorbidities : NR

A vs. B, Median (IQR)

VAS pain (0-10)

Baseline: 6.95 (5.90 to 8.00) vs. 7.45 (6.00 to 8.10)

Long term: 6.0 (3.0 to 8.1) vs. 6.55 (3.80 to 8.00), adjusted OR of improvement from baseline 1.20 (0.63 to 2.30)f

ODI (0-100)

Baseline: 40 (28 to 50) vs. 38 (28 to 50)

Long term: 36 (22 to 49) vs. 38 (28 to 50), adjusted OR of improvement from baseline 1.61 (0.84 to 3.07)f

A vs. B, Median (IQR)

Zung SDS (1-4)

Baseline: 3 (2 to 3) vs. 2 (1 to 3)

Long term: 2 (2 to 3) vs. 2 (2 to 3), adjusted OR 1.31 (0.69 to 2.47)f

Stress and Crisis Inventory (SCI-93) (0-140)

Baseline: 60 (45 to 79) vs. 54.5 (33 to 76)

Long term: 56 (38 to 75) vs. 51 (33 to 76), adjusted OR 1.10 (0.58 to 2.08)f

SF-36 PCS (0-100) g

Baseline: 30 (NR) vs. 30 (NR)

Long term: 31 (NR) vs. 30 (NR)

SF-36 MCS (0-100) g

Baseline: 35 (NR) vs. 39 (NR)

Long term: 40 (NR) vs. 39 (NR)

Harms: NR

Patient Satisfaction (1-7), median (IQR)

-

Felt fully medically assessed: 5 (3 to 7) vs. 3 (1 to 5), p<0.001

-

Received an understandable explanation of the condition: 6 (5 to 7) vs. 3 (1 to 5), p<0.001

-

Would recommend assessment to a friend: 7 (5 to 7) vs. 5 (2 to 7), p<0.001

-

Rehabilitation plan carried out after assessment: 5 (3- to 5) vs. 4 (2 to 5), p=0.004

-

Assessment was helpful: 6 (4 to 7) vs. 4 (2 to 5) , p<0.001

Streibelt 2014

Germany

Mean duration of pain: NR

RCT

Fair

CPMP with vs. without pretreatment assessment

A. CPMP plus pretreatment functional capacity evaluation (FCE) (n=109)

3 weeks, 3 to 4 hours/day (total 50 to 60 hours), individual, inpatient

B. CPMP alone (n=113)

3 weeks, 3 to 4 hours/day (total 50 to 60 hours), individual, inpatient

Mean age: 46 years

% Male: 83%

Race/ethnicity: NR

Pain etiology/type: Chronic MSK disorders

-

M40-M54: 82%

Disability: NR

Currently sick-listed: 81%

Duration of sick leave last year: 15 weeks

Comorbidities: NR

-

Excluded: “physicians’ diagnosis of red flags”

A vs. B, mean

PDI (0-70)

Baseline: 37.4 (14.4) vs. 33.2 (13.6)

Long term: 27.0 vs. 33.5, adjusted difference −6.5 (95% CI −12.6 to – 0.4)h

NRNR

BDI = Beck Depression Inventory; CI = confidence interval; CPMP = comprehensive pain management program; IQR – interquartile range; LBP = low back pain; MCS = Mental Component Score; MPQ = McGill Pain Questionnaire; MSK = musculoskeletal; NR = not reported; NOS = not otherwise specified; ODI = Oswestry Disability Index; OR = odds ratio; PCS = Physical Component Score; PDI = Pain Disability Index; PT = physical therapy; RCT = randomized controlled trial; RDQ = Roland-Morris Disability Index; RR = risk ratio; SD = standard deviation; SF-36 = Short Form 36 Questionnaire; SIP = Sickness Impact Profile; VAS = visual analog scale; WHYMPI = West Haven-Yale Multidimensional Pain Inventory.

a

Demographics data include information for patients in both Part 1 and 2 of this study (demographics were not reported separately by the authors).

b

All followup scores were estimated from graphs in the article. For data included in the meta-analyses, the standard deviation was imputed using average CV of studies under same outcome category. Where means and standard deviations are reported in this table, they came from the results of the meta-analyses.

c

Range of 9 to 18 months with the majority at 12 months.

d

Data were estimated by the EPC from figures in the article.

e

Standard deviations estimated from Figure 2 of article.

f

Multivariate regression adjusted for sex, age, smoking status, nationality, education level, and relationship status.

g

SF-36 scores estimated from Figure 2 of article.

h

Adjusted for baseline score of the outcome, baseline employment status, baseline work ability, baseline PDI and diagnosis.

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