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Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation

Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation, the CR$P-2 Pilot Study.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00372671
Enrollment
60
Registered
2006-09-07
Start date
2005-06-30
Completion date
2005-08-31
Last updated
2017-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Angioplasty, Coronary Artery Bypass Surgery, Myocardial Infarction, Unstable Angina

Keywords

Cardiac Rehabilitation, Improving Cardiac Rehabilitation Participation

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.

Interventions

BEHAVIORALSurvey
BEHAVIORALSurvey and videotape

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Expressed intent to participate in a CRSP program.

Secondary

MeasureTime frame
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.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026