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Sponsored by: |
Lawson Health Research Institute |
Information provided by: | Lawson Health Research Institute |
ClinicalTrials.gov Identifier: | NCT00372671 |
The purpose of this study is to determine whether a pre-discharge videotape introducing the concept and benefit of a Cardiac Rehabiliation & Secondary Prevention (CRSP) program will increase intent to participate in a CRSP program in post myocardial infarction, unstable angina, coronary artery bypass surgery, or coronary angioplasty patients.
Condition | Intervention | Phase |
Myocardial Infarction Unstable Angina Coronary Angioplasty Coronary Artery Bypass Surgery |
Behavioral: Survey Behavioral: Survey and videotape |
Phase III |
MedlinePlus related topics: | Angina Angioplasty Coronary Artery Bypass Surgery Heart Attack Rehabilitation |
Study Type: | Interventional |
Study Design: | Educational/Counseling/Training, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study |
Official Title: | Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation, the CR$P-2 Pilot Study. |
Estimated Enrollment: | 60 |
Study Start Date: | June 2005 |
Estimated Study Completion Date: | August 2005 |
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, unstable angina, angioplasty or coronary artery bypass. However less than 20% of eligible patients participate in CRSP programs. This study will look at a method of potentially improving enrollment and adherence to a CRSP program. Patients will be randomized into two groups. One group will complete a survey and view a videotape introducing the concept of a CRSP program. The second group will be requested to complete a survey only, but will not be exposed to the videotape. It is expected that the patients who view the videotape will be more likely to express intent to participate in CRSP versus those patients who do not view the videotape.
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 |
Lawson Health Research Institute |
Principal Investigator: | Neville Suskin, MBChB, MSc | University of Western Ontario and London Health Sciences Centre |
Study ID Numbers: | R-02-144 |
First Received: | September 6, 2006 |
Last Updated: | September 6, 2006 |
ClinicalTrials.gov Identifier: | NCT00372671 |
Health Authority: | Canada: Health Canada |
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