Cardiac Rehabilitation for Heart Event Recovery (HER)

N/ACompletedNCT01019135

University Health Network, Toronto169 enrolled

Overview

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

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 Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

HEALTH_SERVICES_RESEARCH

Masking

SINGLE

Enrollment

169

Conditions

Myocardial Ischemia Acute Coronary Syndrome Heart Disease Coronary Artery Disease

Interventions

Cardiac RehabilitationBEHAVIORAL

comparison of multiple cardiac rehabilitation program models

Eligibility

Sex: FEMALE

Medical Language ↔ Plain English

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

Locations (5)

Hamilton Health Sciences Centre

Hamilton, Ontario, Canada

Mount Sinai

Toronto, Ontario, Canada

Toronto Rehabilitation Institute

Toronto, Ontario, Canada

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada

Outcomes

Primary Outcomes

CR Program Adherence

Time frame: 6 months

Secondary Outcomes

Exercise Capacity

Exercise capacity as measured by VO2peak on a graded stress test.

Time frame: 6 months

Exercise

Mean daily steps as measured by a pedometer over 7 days

Time frame: 6 months

Self-reported Exercise

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.

Time frame: 6 months

Diet

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.

Time frame: 6 months

Medication Adherence

Data from ClinicalTrials.gov

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