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Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation

L

Lawson Health Research Institute

Status and phase

Completed
Phase 3

Conditions

Unstable Angina
Myocardial Infarction
Coronary Angioplasty
Coronary Artery Bypass Surgery

Treatments

Behavioral: Survey
Behavioral: Survey and videotape

Study type

Interventional

Funder types

Other

Identifiers

NCT00372671
R-02-144

Details and patient eligibility

About

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.

Full 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.

Sex

All

Ages

18+ years old

Volunteers

Accepts 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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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