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The Efficacy and Economics of Exercise Maintenance Post-Cardiac Rehabilitation (ECOPCR)

Primary Purpose

Coronary Artery Disease

Status

Completed

Phase

Not Applicable

Locations

Canada

Study Type

Interventional

Intervention

Exercise Facilitator Intervention

About this trial

This is an interventional prevention trial for Coronary Artery Disease focused on measuring Coronary Artery Disease, Cardiac Rehabilitation, Exercise Maintenance, Facilitator, Managed Home Exercise, Community Based Exercise

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patient is currently participating in an on-site CR program of ≥ 8-week duration (to ensure that outcomes are not confounded by exposure to home-based or telephone-based case managed programs)
Patient has graduated from CR (to ensure that the study is evaluating an intervention to help sustain and improve maintenance of exercise behaviour
Patient has a documented diagnosis of CAD (to ensure homogeneity of the patient population)
Patient is 18 years of age or older
Patient is able and willing to provide informed consent
Able to walk unaided at 2 mph

Exclusion Criteria:

Patient has New York Heart Association class III or IV heart failure (because this might interfere with the ability to achieve recommended exercise levels and to ensure homogeneity of the patient population)
Patient is pregnant, lactating or planning to become pregnant during the study period (because this might interfere with the ability to achieve recommended exercise levels)
Patient is unable to read and understand English or French
Planning to leave the province or region in the next 12 months
Member of the participant's household is already participating in the study
The participant is unable, in the opinion of the qualified investigator, to participate in unsupervised exercise.

Sites / Locations

University of Ottawa Heart Institute
York University and University Health Network

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Exercise Facilitator Intervention

Usual Care

Arm Description

The intervention employs small group counseling teleconferences (5),personal telephone contacts (3) and community Heart Wise Exercise program demonstrations.

Usual care for cardiac rehab graduates provided by the University of Ottawa Heart Institute Minto Prevention & Rehabilitation Centre and the Cardiovascular Rehabilitation and Prevention Centre at the University Health Network.

Outcomes

Primary Outcome Measures

9-day accelerometer-measured physical activity of moderate and vigorous intensity

Physical activity will be measured directly by having participants wear the Actigraph GT3X accelerometer (Actigraph, Pensacola, Florida) over the right hip for a 9-day recording period, excluding periods when they are sleeping, swimming, or bathing. The activity monitor provides measurements including activity counts, energy expenditure, and step counts, in addition to activity intensity levels. Participants will be considered to be maintaining exercise at guideline recommended levels if they undertake ≥ 30 minutes of moderate and/or vigorous intensity physical activity on ≥ five days.

Secondary Outcome Measures

Symptom limited graded exercise test with electrocardiographic monitoring using a ramp protocol on a treadmill

A random sub-sample of participants (N = 124) will complete a symptom limited graded exercise test with electrocardiographic monitoring using a ramp protocol on a treadmill at baseline and at 52 weeks. Exercise tolerance will also be assessed using the Duke Activity Status Index (DASI), a self-administered questionnaire that measures a patient's functional capacity and is used as an estimate of an individual's peak oxygen uptake

Quality of life measured by the the EuroQoL 5D

The EQ-5D is the current gold standard measure of generic quality of life, has been used in numerous studies and has been validated in many languages. The EQ-5D consists of 2 pages - the EQ-5D descriptive system and the EQ visual analogue scale. The EQ-5D descriptive system comprises the following 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.

Cardiovascular risk factors measured by body mass index and blood pressure.

Height and weight is measured for the determination of body mass index (BMI). Waist circumference is measured using a non-stretchable standard tape measure. Systolic blood pressure is measured in a seated position after a five-minute rest period using an automated, non-invasive blood pressure monitor (BPTru) that automatically performs six measurements

Enrollment in Heart Wise Exercise programs

Enrollment in community-based and Heart Wise Exercise programs will be queried in the follow-up surveys.

Mediators of Intervention Effect

1.Physical activity history 2.Physical activity self-regulation 3. Action planning 4. Intentions to exercise 5. Beliefs about the benefits of and barriers to exercise 5. Task self-efficacy 6. Barrier self-efficacy 7. Social support from family and friends 8. Autonomy support derived from health care providers 9. Home exercise equipment 10. Neighbourhood environmental attributes of walkability and access to recreation facilities 11. Adherence to medications

Cost-effectiveness and cost-utility

Health effects are measured by overall survival time; event-free time from myocardial infarction, revascularization or death; and quality adjusted life years. Participants are linked to health administrative data to allow health care utilization to be tracked. Participants complete a monthly diary to record time for counseling and physical activities, out-of-pocket expenses, and items related to productivity, including lost work days, home care expenses due to reduced function or cardiac disability. Data is collected on the resources expended for each intervention.

Full Information

NCT ID

NCT01658683

First Posted

August 1, 2012

Last Updated

February 24, 2022

Sponsor

Ottawa Heart Institute Research Corporation

Collaborators

Heart and Stroke Foundation of Ontario

1. Study Identification

Unique Protocol Identification Number

NCT01658683

Brief Title

The Efficacy and Economics of Exercise Maintenance Post-Cardiac Rehabilitation

Acronym

ECOPCR

Official Title

Ecologically Optimizing Exercise Maintenance in Men and Women Post-Cardiac Rehabilitation: A Randomized Controlled Trial of Efficacy With Economics

Study Type

Interventional

2. Study Status

Record Verification Date

February 2022

Overall Recruitment Status

Completed

Study Start Date

October 2012 (Actual)

Primary Completion Date

March 2018 (Actual)

Study Completion Date

July 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Ottawa Heart Institute Research Corporation

Collaborators

Heart and Stroke Foundation of Ontario

4. Oversight

Data Monitoring Committee

5. Study Description

Brief Summary

The purpose of this study is to develop a new intervention to improve the transition of patients from structured, supervised exercise to self-managed home- or approved community-based exercise programs in an effort to increase maintenance of exercise behaviour post cardiac rehabilitation (CR). The goal of the study is that those receiving the intervention will engage in at least 30 minutes of physical activity at a moderate or vigorous intensity 5 or more days per week, 26, 52 and 78 weeks after CR compared to those in the usual care group. The new intervention will be delivered by trained exercise facilitators (physiotherapists or exercise specialists) and will make use of: small group counseling teleconferences (5 sessions); personal telephone contacts (3 sessions), and community program demonstrations that would facilitate linkages between patients and approved community programs known as Heart Wise Exercise programs available in Ottawa and Toronto. The trial will be conducted at the Minto Prevention and Rehabilitation Centre at the University of Ottawa Heart Institute and the Cardiovascular Rehabilitation and Prevention Centre at the University Health Network (Peter Munk Cardiac Centre [PMCC] and Toronto Rehabilitation Institute [TRI]) sites. The study has a target enrollment of 604 participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Coronary Artery Disease

Keywords

Coronary Artery Disease, Cardiac Rehabilitation, Exercise Maintenance, Facilitator, Managed Home Exercise, Community Based Exercise

7. Study Design

Primary Purpose

Prevention

Study Phase

Not Applicable

Interventional Study Model

Parallel Assignment

Masking

Investigator

Allocation

Randomized

Enrollment

451 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Exercise Facilitator Intervention

Arm Type

Experimental

Arm Description

The intervention employs small group counseling teleconferences (5),personal telephone contacts (3) and community Heart Wise Exercise program demonstrations.

Arm Title

Usual Care

Arm Type

No Intervention

Arm Description

Intervention Type

Behavioral

Intervention Name(s)

Exercise Facilitator Intervention

Intervention Description

The 50 week intervention includes 5 small group counseling teleconferences, 3 personal telephone calls and Heart Wise Exercise program demonstrations. During the teleconferences and personal telephone calls, the facilitator discusses the importance of exercise. Participants review their activity diaries, identify barriers to exercise maintenance experienced to date and brainstorm solutions as a group. In addition, the facilitator conducts community program demonstrations at Heart Wise Exercise program locations in Ottawa and Toronto for interested participants.

Primary Outcome Measure Information:

Title

9-day accelerometer-measured physical activity of moderate and vigorous intensity

Description

Time Frame

78 weeks

Secondary Outcome Measure Information:

Title

Symptom limited graded exercise test with electrocardiographic monitoring using a ramp protocol on a treadmill

Description

Time Frame

52 weeks

Title

Quality of life measured by the the EuroQoL 5D

Description

Time Frame

78 weeks

Title

Cardiovascular risk factors measured by body mass index and blood pressure.

Description

Time Frame

78 weeks

Title

Enrollment in Heart Wise Exercise programs

Description

Enrollment in community-based and Heart Wise Exercise programs will be queried in the follow-up surveys.

Time Frame

78 weeks

Title

Mediators of Intervention Effect

Description

Time Frame

78 weeks

Title

Cost-effectiveness and cost-utility

Description

Time Frame

78 weeks

10. Eligibility

Sex

All

Minimum Age & Unit of Time

18 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Patient is currently participating in an on-site CR program of ≥ 8-week duration (to ensure that outcomes are not confounded by exposure to home-based or telephone-based case managed programs) Patient has graduated from CR (to ensure that the study is evaluating an intervention to help sustain and improve maintenance of exercise behaviour Patient has a documented diagnosis of CAD (to ensure homogeneity of the patient population) Patient is 18 years of age or older Patient is able and willing to provide informed consent Able to walk unaided at 2 mph Exclusion Criteria: Patient has New York Heart Association class III or IV heart failure (because this might interfere with the ability to achieve recommended exercise levels and to ensure homogeneity of the patient population) Patient is pregnant, lactating or planning to become pregnant during the study period (because this might interfere with the ability to achieve recommended exercise levels) Patient is unable to read and understand English or French Planning to leave the province or region in the next 12 months Member of the participant's household is already participating in the study The participant is unable, in the opinion of the qualified investigator, to participate in unsupervised exercise.

Overall Study Officials: