- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00372671
Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation
August 24, 2017 updated by: Lawson Health Research Institute
Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation, the CR$P-2 Pilot Study.
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
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.
Study Type
Interventional
Enrollment
60
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
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London, Ontario, Canada, N6A 5A5
- London Health Sciences Centre
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Admission to hospital for MI, UA, PTCA or CABS
Exclusion Criteria:
- Inability to provide written informed consent or complete the survey for any reason
- Previous CRSP participation
- Patients who are scheduled to undergo coronary artery bypass surgery within 3 months following the index hospital discharge
- Patients with an inability to exercise due to musculoskeletal problems or previous stroke
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Expressed intent to participate in a CRSP program.
|
Secondary Outcome Measures
Outcome Measure |
---|
Number of patients who continue to adhere to the 6-month CRSP program beyond the initial expressed intent to participate.
|
Impact of other patient variables and how they influence participation in a CRSP program.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Neville Suskin, MBChB, MSc, University of Western Ontario and London Health Sciences Centre
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2005
Primary Completion (Actual)
August 1, 2005
Study Completion (Actual)
August 1, 2005
Study Registration Dates
First Submitted
September 6, 2006
First Submitted That Met QC Criteria
September 6, 2006
First Posted (Estimate)
September 7, 2006
Study Record Updates
Last Update Posted (Actual)
August 25, 2017
Last Update Submitted That Met QC Criteria
August 24, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R-02-144
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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