N/A
N=169
Cardiac Rehabilitation for Heart Event Recovery (HER)
Myocardial Ischemia · Acute Coronary Syndrome · Heart Disease · Coronary Artery Disease
Bottom Line
View on ClinicalTrials.gov: NCT01019135 ↗Enrolled (actual)
169
Serious AEs
0.0%
Results posted
Nov 2015
Primary outcome: Primary: CR Program Adherence — 54.40; 51.33; 58.12 percentage of sessions attended
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Cardiac Rehabilitation (Behavioral)
- Age
- Pediatric, Adult, Older Adult
- Sex
- Female
- Sponsor
- University Health Network, Toronto
- Primary completion
- Mar 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY CR Program Adherence |
54.40; 51.33; 58.12 | — |
| SECONDARY Exercise Capacity |
21.6071; 20.8450; 21.0734 | — |
| SECONDARY Exercise |
5296.9660; 6129.7143; 6694.3308 | — |
| SECONDARY Self-reported Exercise |
31.3243; 31.4; 29.5645 | — |
| SECONDARY Diet |
202.2019; 202.3477; 213.9834 | — |
| SECONDARY Medication Adherence |
3.6842; 3.5238; 3.5833 | — |
| SECONDARY Smoking |
1; 3; 3 | — |
Summary
The purpose of this study is to compare women's cardiac rehabilitation program adherence across three program models.
Eligibility Criteria
Inclusion Criteria
- Documented coronary artery disease and/or acute coronary syndrome diagnosis and/or revascularization (coronary bypass graft or angioplasty) and/or valve surgery
- Work or reside in Greater Toronto Area
- Proficiency in English language
- Written approval to participate in CR by the patient's cardiac specialist or general practitioner
- Eligible for home-based CR
Exclusion Criteria
- musculoskeletal, neuromuscular, visual, cognitive or non-dysphoric psychiatric condition, or any serious or terminal illness not otherwise specified which would preclude CR eligibility based on CR guidelines
- physician deems patient not suitable for CR at time of intake exercise stress test
- planning to leave the area prior to the anticipated end of participation
- being discharged to a long-term care facility
- participation in another clinical trial with behavioral interventions
Data sourced from ClinicalTrials.gov (NCT01019135). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.