A Clinical Trial of a Self-Management Education Program for People With Chronic Stable Angina

Phase 1

• Conditions: Chronic Stable Angina

• Registration Number: NCT00350922
• Lead Sponsor: University of Toronto

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2003-09
• Status Verified: 2005-11
• Study Completion: 2005-11
• Study First Submitted: 2006-07-08
• Study First Submitted QC: 2006-07-08
• Last Update Submitted: 2006-07-08
• Study First Posted: 2006-07-11
• Last Update Posted: 2006-07-11

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 130

Inclusion Criteria

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

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Exclusion Criteria

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

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
SF36
Seattle Angina Questionnaire

Secondary Outcome Measures

Name	Time	Method
Self-Efficacy Scale
Self-Control Schedule

Trial Locations

Locations (1)

University of Toronto; 🇨🇦 Toronto, Ontario, Canada