| Study-level data |
|---|
| Centre ID | Centre name |
| Randomised control patients (n) | |
| Randomised exercise patients (n) | |
| Patient-level data: descriptive |
|---|
| Patient ID | |
| Date of randomisation | dd/mm/yyyy |
| Allocated treatment |
1. Exercise
2. Control
|
| Date of birth | dd/mm/yyyy |
| Gender |
1. Male
2. Female
9. Data unavailable
|
| Race |
1. White/Caucasian
2. African/African-American
3. Asian
4. Other
9. Data unavailable
|
| Aetiology of HF |
1. Ischaemic heart disease
2. Idiopathic dilated cardiomyopathy
3. Other/unknown
9. Data unavailable
|
| Year of HF diagnosis | yyyy |
| NYHA class at entry/baseline |
1. NYHA class I
2. NYHA class II
3. NYHA class III
4. NYHA class IV
9. Unknown/unavailable
|
| Ejection fraction at entry/baseline (%) | |
| Patient level data: outcomes |
|---|
| Method of exercise capacity assessment |
1. 6MWT
2. Bicycle ergometer test
3. Treadmill test
4. Other (state)
|
| Exercise capacity score at entry (units) |
| Follow-up 1 exercise capacity score | Follow-up time (months) |
| Follow-up 2 exercise capacity score | Follow-up time (months) |
| Follow-up 3 exercise capacity score | Follow-up time (months) |
| HRQoL |
1. MLHFQ
2. Other measure (state)
|
| HRQoL at entry | Total and subscores |
| Follow-up 1 HRQoL score |
Total and subscores
Follow-up time (months)
|
| Follow-up 2 HRQoL score |
Total and subscores
Follow-up time (months)
|
| Follow-up 3 HRQoL score |
Total and subscores
Follow-up time (months)
|
| Date of death | dd/mm/yyyy |
| Cause of death |
1. Acute myocardial infarction
2. Sudden death
3. Heart failure
4. Other cardiac
5. Stroke
6. Other vascular/thromboembolic
7. Non-cardiovascular
8. Unknown
(1–4, cardiac; 1–6, cardiovascular)
|
| Date of first all-cause hospital admission |
dd/mm/yyyy
1. De novo hospitalisation
2. Rehospitalisation
|
| Date of first HF hospital admission |
dd/mm/yyyy
1. De novo hospitalisation
2. Rehospitalisation
|
| Number of all-cause hospitalisations | |
| Number of all HF hospitalisations | |
| Dropout |
|---|
| Date of study discontinuation | dd/mm/yyyy |
| Reason for study discontinuation | |
| Exercise training (applies only to exercise group patients) |
| Study-level data |
|---|
| Prescribed exercise training |
| Overall duration | — weeks (ranges if appropriate) |
| Session duration | — minutes (range if appropriate) |
| Frequency of sessions | — sessions/week (range if appropriate) |
| Intensity | — % units (range if appropriate) |
| Setting |
1. Centre only
2. Home only
3. Both centre and home (define proportion of sessions at each location)
4. Other (state)
|
| Patient-level data |
|---|
| Attended first exercise training |
1. Yes
2. No
3. Not reported
|
| Are details available at patient level on exercise dose received? |
1. Yes
2. No
|
