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Sponsors and Collaborators: |
Lawson Health Research Institute Canadian Institutes of Health Research (CIHR) AstraZeneca |
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Information provided by: | Lawson Health Research Institute |
ClinicalTrials.gov Identifier: | NCT00336830 |
The purpose of this study is to determine the effect of a pre-discharge written personal endorsement to the patient by the patient's attending cardiologist or cardiac surgeon (MD endorsement) to take part in the Cardiac Rehabilitation and Secondary Prevention (CR) program, in addition to the standard CR referral, compared to the standard CR referral alone, on CR program enrollment within 2 months of index hospital discharge following admission for myocardial infarction, unstable angina, coronary angioplasty, or coronary artery bypass.
Condition | Intervention | Phase |
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Myocardial Infarction Unstable Angina Coronary Disease |
Behavioral: MD-endorsed Cardiac Rehabilitation referral Behavioral: Standard Cardiac Rehabilitation referral |
Phase III |
Study Type: | Interventional |
Study Design: | Randomized, Single Blind (Subject), Active Control, Parallel Assignment, Efficacy Study |
Official Title: | Improving Cardiac Rehabilitation Participation in Women and Men |
Estimated Enrollment: | 1035 |
Study Start Date: | May 2003 |
Estimated Study Completion Date: | December 2008 |
Primary Completion Date: | June 2007 (Final data collection date for primary outcome measure) |
There is compelling evidence that a comprehensive CR program comprising the delivery of lifestyle modifying education will reduce mortality, morbidity and improve quality of life in patients following myocardial infarction, angioplasty or, coronary artery bypass. However, less than 20% of eligible patients participate in CR programs. This study will look at a method of potentially improving enrollment and adherence to a CR program. It is expected that patients who receive the MD-endorsed referral will be more likely to attend the initial Orientation appointment and more closely adhere to the 6-month comprehensive CR program, as compared to the patients who receive a standard CR referral alone.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Canada, Ontario | |
London Health Sciences Centre | |
London, Ontario, Canada, N6A 5A5 |
Principal Investigator: | Neville Suskin, MBChB, MSc | University of Western Ontario & London Health Sciences Centre |
Responsible Party: | Lawson Health Research Institute ( Dr. Neville Suskin ) |
Study ID Numbers: | R-02-037, CIHR 56926 |
Study First Received: | June 13, 2006 |
Last Updated: | July 25, 2008 |
ClinicalTrials.gov Identifier: | NCT00336830 |
Health Authority: | Canada: Health Canada |
Cardiac Rehabilitation Improving Cardiac Rehabilitation Participation coronary angioplasty coronary artery bypass surgery |
Arterial Occlusive Diseases Heart Diseases Myocardial Ischemia Angina Pectoris Vascular Diseases Pain Arteriosclerosis Ischemia |
Chest Pain Coronary Disease Signs and Symptoms Necrosis Infarction Myocardial Infarction Angina, Unstable Coronary Artery Disease |
Pathologic Processes Cardiovascular Diseases |