We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00372671
First Posted: September 7, 2006
Last Update Posted: August 25, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Lawson Health Research Institute
  Purpose
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 3

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Primary Purpose: Other
Official Title: Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation, the CR$P-2 Pilot Study.

Resource links provided by NLM:


Further study details as provided by Lawson Health Research Institute:

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.

Estimated Enrollment: 60
Actual Study Start Date: June 2005
Study Completion Date: August 2005
Primary Completion Date: August 2005 (Final data collection date for primary outcome measure)
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.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00372671


Locations
Canada, Ontario
London Health Sciences Centre
London, Ontario, Canada, N6A 5A5
Sponsors and Collaborators
Lawson Health Research Institute
Investigators
Principal Investigator: Neville Suskin, MBChB, MSc University of Western Ontario and London Health Sciences Centre
  More Information

Responsible Party: Lawson Health Research Institute
ClinicalTrials.gov Identifier: NCT00372671     History of Changes
Other Study ID Numbers: R-02-144
First Submitted: September 6, 2006
First Posted: September 7, 2006
Last Update Posted: August 25, 2017
Last Verified: August 2017

Keywords provided by Lawson Health Research Institute:
Cardiac Rehabilitation
Improving Cardiac Rehabilitation Participation

Additional relevant MeSH terms:
Infarction
Myocardial Infarction
Angina, Unstable
Ischemia
Pathologic Processes
Necrosis
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases
Angina Pectoris
Chest Pain
Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms