Methods	Prospecitve, single centre RCT in the US. F/U 6 months.
Participants	N= 88 (EX n=41; CON n=47) 100% male Mean age: EX= 62 +/−8, CON = 63 +/−7; (range 42 - 72) Diagnosis: CAD and a physical disability Ethnicity: NR Inclusion: ≤73 years; CAD and physical disability. CAD documented by history of MI, coronary artery bypass surgery, percutaneous transluminal coronary angioplasty or angiographically demonstrated CAD; have the functional use ofmore than 2 extremities, 1 being an arm, in order to perform the exercise test and training protocols Exclusion: uncontrolled hypertension or diabetes mellitus, clinically significant cardiac dysrhythmias, unstable angina pectoris, cognitive deficits, or other problems that would interfere with compliance to the prescribed exercise and diet protocol
Interventions	Exercise group (Home exercise training programme): Duration: 6 months; Frequency: 5 days/week; Session duration: 20mins/day; Intensity: 85% of predicted maximal heart rate Mode: stationary wheelchair ergometer Control group: routine care
Outcomes	Total mortality, non fatal MI at 6 months
Notes	The treatment programme decreased myocardial oxygen demand.
Risk of bias
Bias	Authors’ judgement	Support for judgement
Random sequence generation (selection bias)	Unclear risk	“randomized”
Allocation concealment (selection bias)	Unclear risk	Not reported.
Blinding (performance bias and detection bias) All outcomes	Low risk	“The same experienced cardiologist interpreted all echocardiograms and was unaware of randomization procedures”
Incomplete outcome data (attrition bias) All outcomes	High risk	32% lost to follow up, no description of withdrawals or dropouts
Selective reporting (reporting bias)	Unclear risk	No information reported.