Investigating the Effects of Cardiac Rehabilitation eXercise Modalities on Physical and Mental Health Outcomes (CRX-Modalities)

University of Ottawa Heart Institute

Status: Completed

Conditions: Coronary Artery Disease (CAD)

Treatments: Behavioral: High Intensity Interval Training; Behavioral: Nordic Walking; Behavioral: Moderate Intensity Continuous Exercise Training

Study type: Interventional

Funder types: Other

Identifiers

NCT02765568

20160127-01H

Details and patient eligibility

About

Coronary revascularization improves survival for patients with coronary artery disease. However,many patients are left with poor physical and mental health. Traditional cardiac rehabilitation involves moderate intensity continuous exercise (MICE). Alternatives to traditional cardiac rehabilitation programming may however provide superior understudied benefits to patients with poor physical and mental health. Nordic walking (NW) and high-intensity interval training (HIIT) are two examples of alternative programs for cardiac rehabilitation, which may provide superior physical and mental health benefits when compared to traditional MICE. The main purpose of this project is, therefore, to determine the short and long term physical and mental health benefits of alternative cardiac rehabilitation modalities, including NW and HIIT on exercise capacity, quality of life and depression after a 12-week program.

Enrollment: 135 patients

Sex: All

Ages: 40 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient with CAD who recently underwent PCI (within 2-10 weeks) PCI or coronary artery bypass grafting (within the last 18 weeks);
• Patient is referred to University of Ottawa Heart Institute cardiac rehabilitation program;
• Patient is able to walk independently
• Patient is willing to attend an onsite cardiac rehabilitation program twice weekly for 12 weeks;
• At least 40 years of age;
• Patient is willing and able to provide informed consent

Exclusion criteria

• Currently participating in routine exercise training (>2x/week) and/or using Nordic Walking poles;
• Active infection or inflammatory condition;
• Over 75 years of age;
• Persistent or permanent atrial fibrillation;
• Pregnant, lactating or planning to become pregnant during the trial period;
• Unstable angina or established diagnosis of chronic obstructive pulmonary disease, severe mitral or aortic stenosis, or hypertrophic obstructive cardiomyopathy;
• Unable to read and understand English or French;
• Unwilling or unable to return for follow-up visit at weeks 12 and 26;

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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135 participants in 3 patient groups

Moderate Intensity Continuous Exercise

Experimental group

Description:

Moderate Intensity Continuous Exercise Training

Treatment:

Behavioral: Moderate Intensity Continuous Exercise Training

Nordic Walking

Experimental group

Description:

Nordic Walking

Treatment:

Behavioral: Nordic Walking

High Intensity Interval Training

Experimental group

Description:

High Intensity Interval Training

Treatment:

Behavioral: High Intensity Interval Training