Cardiac Rehabilitation for Heart Event Recovery (HER)

Not Applicable

Completed

• Conditions: Acute Coronary Syndrome; Coronary Artery Disease; Myocardial Ischemia; Heart Disease
• Interventions: Behavioral: Cardiac Rehabilitation

• Registration Number: NCT01019135
• Lead Sponsor: University Health Network, Toronto

Brief Summary

The purpose of this study is to compare women's cardiac rehabilitation program adherence across three program models.

Detailed Description

Heart disease is the leading cause of morbidity and mortality for women in Canada. Cardiac rehabilitation (CR) is an outpatient secondary prevention program composed of structured exercise and comprehensive education and counseling. CR participation results in lower morbidity and mortality, among other benefits. Unfortunately, women are significantly less likely to adhere to these programs than men. While the traditional model of CR care is a hospital-based mixed-sex program, women are the minority in such programs, and state that these programs do not meet their care preferences. Two other models of CR care have been developed: hospital-based women-only (sex-specific) and monitored home-based programs. Other than through our controlled pilot testing of 36 patients, women's adherence to these program models is not well known.

CR4HER is a 3 parallel arm pragmatic RCT designed to compare program adherence to traditional hospital-based CR with males and females, home-based CR, and women-only hospital-based CR. Power calculations based on our pilot study suggest a sample size of 261 patients is needed to detect a difference in adherence by program model using ANCOVA. Participants are female CAD, acute coronary syndrome, percutaneous coronary intervention, bypass surgery, or valve surgery inpatients recruited from 5 hospitals. Also, female patients referred to participating cardiac rehabilitation (3) centres with one of the aforementioned diagnosis will be approached to participate. The primary outcome variable is program adherence operationalized as CR site-reported percentage of prescribed sessions completed by phone or on-site, as reported by a staff member who is blind to study objectives. Secondary outcomes are exercise capacity operationalized as VO2peak on a graded stress test, and exercise, dietary, smoking and medication adherence behaviours measured in hospital and 1 week post-CR. By identifying the CR program model which results in the greatest adherence for women, we can optimize their participation and potentially their cardiac outcomes.

Study Timeline

• Study Start: 2009-11
• Study First Submitted: 2009-11-20
• Study First Submitted QC: 2009-11-23
• Study First Posted: 2009-11-25
• Primary Completion: 2014-03
• Study Completion: 2014-03
• Results First Submitted: 2015-06-23
• Status Verified: 2015-10
• Results First Submitted QC: 2015-10-28
• Last Update Submitted: 2015-10-28
• Results First Posted: 2015-11-30
• Last Update Posted: 2015-11-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 169

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

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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

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Home-Based Cardiac Rehabilitation	Cardiac Rehabilitation	In the monitored home-based programs, patients attend an intake appointment where an exercise test is performed as the basis for exercise prescription. Patients are given written guidelines for aerobic conditioning based on their treadmill test. Patients are cautioned about symptoms, and taught how to check their heart rate during walking sessions. Patients are provided with reading materials regarding CVD, risk factors and lifestyle modification. These are discussed with an allied health professional from the home-based CR program by telephone during weekly scheduled telephone calls.
Women-Only Cardiac Rehabilitation	Cardiac Rehabilitation	The women-only CR programs include on-site group exercise training sessions 1-2 days/week. Participants are encouraged to walk at home on alternate days of the week. Education sessions are also given in a group format, wherein participants engage in on-site female-only group exercise sessions, as well as female-only group education sessions.
Co-ed Cardiac Rehabilitation	Cardiac Rehabilitation	The traditional hospital-based co-ed CR programs include on-site group exercise training sessions 1-2 days/week. Participants are encouraged to walk at home on alternate days of the week. Education sessions are also given in a group format.

Primary Outcome Measures

Name	Time	Method
CR Program Adherence	6 months

Secondary Outcome Measures

Name	Time	Method
Medication Adherence	6 months	The 4-item Morisky Medication Adherence Scale was used, which is scored as yes = 0, no = 1, such that a higher score indicates higher medication adherence. Scores range from 0 to 4, with patients scoring 2 or above considered adherent.
Exercise	6 months	Mean daily steps as measured by a pedometer over 7 days
Self-reported Exercise	6 months	The Godin Leisure-time Exercise Questionnaire will be administered in the pre and post-test surveys. It is a brief and reliable instrument to assess usual leisure-time physical activity behaviour during a one-week period. For the first question, weekly frequencies of strenuous, moderate, and light activities are multiplied by nine, five, and three, respectively. Part two of the questionnaire calculates the frequency of weekly leisure-time activities pursued. Total weekly leisure activity is calculated by summing the products of the separate components. Scores begin at zero, with higher scores indicating greater physical activity. For example, scores equal to or greater than 20 are indicative of someone who is "active". There is no max score.
Exercise Capacity	6 months	Exercise capacity as measured by VO2peak on a graded stress test.
Diet	6 months	The Diet Habit Survey was used to assess diet. It is an inexpensive, reliable, and valid instrument for rapid assessment of eating habits and diet composition. Its 9 questions are related to the consumption of cholesterol, saturated fat, complex carbohydrate (including fiber), and salt.; Greater scores indicate better diets, both for the total score and for each area. The total score indicates the level of fat in the diet (with scores equal to or greater than 236 corresponding to a low-fat diet 20% or less). Scores can begin at 56 and have no upper range.
Smoking	6 months	Current smoking status

Trial Locations

Locations (5)

Sunnybrook Health Sciences Centre; 🇨🇦 Toronto, Ontario, Canada

Hamilton Health Sciences Centre; 🇨🇦 Hamilton, Ontario, Canada

Toronto Rehabilitation Institute; 🇨🇦 Toronto, Ontario, Canada

Mount Sinai; 🇨🇦 Toronto, Ontario, Canada

University Health Network; 🇨🇦 Toronto, Ontario, Canada