NCT00350922UnknownPhase 1
A Psychoeducation Trial for People With Chronic Stable Angina
University of Toronto1 site in 1 country130 target enrollmentStarted: September 1, 2003Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 1
- Sponsor
- University of Toronto
- Enrollment
- 130
- Locations
- 1
- Primary Endpoint
- SF36
Study 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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 0 Years to — (Child, Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
Investigators
Study Sites (1)
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