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Clinical Trials/NCT00350922
NCT00350922
Unknown
Phase 1

A Psychoeducation Trial for People With Chronic Stable Angina

University of Toronto1 site in 1 country130 target enrollmentSeptember 2003
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ConditionsChronic Stable Angina

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Chronic Stable Angina
Sponsor
University of Toronto
Enrollment
130
Locations
1
Primary Endpoint
SF36
Last Updated
19 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this clinical trial was to determine the effectiveness of a supportive and educational self-management program for improving health-related quality of life (HRQOL), angina symptoms, and self-efficacy and resourcefulness to self-manage for chronic angina patients. 130 participants were enrolled in the trial for 3 months. The program, entitled the Chronic Angina Self-Management Program, (CASMP) was found effective for improving HRQOL, angina symptoms, and self-efficacy to manage symptoms, compared to usual care.

Registry
clinicaltrials.gov
Start Date
September 2003
End Date
November 2005
Last Updated
19 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Medical diagnosis of coronary artery disease CCS Class I-III Angina for at least 6 months Speak, read, understand English -

Exclusion Criteria

  • •MI/Bypass last 6 months CCS Class IV angina A major cognitive disorder -

Outcomes

Primary Outcomes

SF36

Seattle Angina Questionnaire

Secondary Outcomes

  • Self-Efficacy Scale
  • Self-Control Schedule

Study Sites (1)

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