Back to resultsA Clinical Trial of a Self-Management Education Program for People With Chronic Stable Angina
Primary Purpose
Chronic Stable Angina
Status
Unknown status
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Psychoeducation
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Stable Angina
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 -
Sites / Locations
- University of Toronto
Outcomes
Primary Outcome Measures
SF36
Seattle Angina Questionnaire
Secondary Outcome Measures
Self-Efficacy Scale
Self-Control Schedule
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00350922
Brief Title
A Clinical Trial of a Self-Management Education Program for People With Chronic Stable Angina
Official Title
A Psychoeducation Trial for People With Chronic Stable Angina
Study Type
Interventional
2. Study Status
Record Verification Date
November 2005
Overall Recruitment Status
Unknown status
Study Start Date
September 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2005 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
University of Toronto
4. Oversight
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Stable Angina
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
130 (false)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
Psychoeducation
Primary Outcome Measure Information:
Title
SF36
Title
Seattle Angina Questionnaire
Secondary Outcome Measure Information:
Title
Self-Efficacy Scale
Title
Self-Control Schedule
10. Eligibility
Sex
All
Minimum Age & Unit of Time
0 Years
Accepts Healthy Volunteers
No
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 -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Judy H Watt-Watson, PhD
Organizational Affiliation
University of Toronto
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Michael H McGillion, PhD
Organizational Affiliation
University of Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Toronto
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5T 1P8
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
A Clinical Trial of a Self-Management Education Program for People With Chronic Stable Angina
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