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Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation

Primary Purpose

Myocardial Infarction, Unstable Angina, Coronary Angioplasty

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Survey
Survey and videotape
Sponsored by
Lawson Health Research Institute
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional other trial for Myocardial Infarction focused on measuring Cardiac Rehabilitation, Improving Cardiac Rehabilitation Participation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • London Health Sciences Centre

Outcomes

Primary Outcome Measures

Expressed intent to participate in a CRSP program.

Secondary Outcome Measures

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.

Full Information

First Posted
September 6, 2006
Last Updated
August 24, 2017
Sponsor
Lawson Health Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00372671
Brief Title
Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation
Official Title
Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation, the CR$P-2 Pilot Study.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
June 2005 (Actual)
Primary Completion Date
August 2005 (Actual)
Study Completion Date
August 2005 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lawson Health Research Institute

4. Oversight

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction, Unstable Angina, Coronary Angioplasty, Coronary Artery Bypass Surgery
Keywords
Cardiac Rehabilitation, Improving Cardiac Rehabilitation Participation

7. Study Design

Primary Purpose
Other
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
60 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Survey
Intervention Type
Behavioral
Intervention Name(s)
Survey and videotape
Primary Outcome Measure Information:
Title
Expressed intent to participate in a CRSP program.
Secondary Outcome Measure Information:
Title
Number of patients who continue to adhere to the 6-month CRSP program beyond the initial expressed intent to participate.
Title
Impact of other patient variables and how they influence participation in a CRSP program.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Neville Suskin, MBChB, MSc
Organizational Affiliation
University of Western Ontario and London Health Sciences Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5A5
Country
Canada

12. IPD Sharing Statement

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Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation

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