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

• Sponsor: University of Toronto (Other)
• Overall Status: Unknown status
• CT.gov ID: NCT00350922
• Collaborator: (none)
• Enrollment: 130
• Location: 1
• Duration (Months): 26
• Patients Per Site Per Month: 5

Study Details

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.

Condition or Disease	Intervention/Treatment	Phase
Chronic Stable Angina	Behavioral: Psychoeducation	Phase 1

Study Design

• Study Type: Interventional
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Psychoeducation Trial for People With Chronic Stable Angina
• Study Start Date: Sep 1, 2003
• Study Completion Date: Nov 1, 2005

Outcome Measures

Primary Outcome Measures

1. SF36 []

2. Seattle Angina Questionnaire []

Secondary Outcome Measures

1. Self-Efficacy Scale []

2. Self-Control Schedule []

Eligibility Criteria

Criteria

• Ages Eligible for Study: 0 Years and Older
• Sexes Eligible for Study: 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 -

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University of Toronto	Toronto	Ontario	Canada	M5T 1P8

Sponsors and Collaborators

• University of Toronto

Investigators

• Study Director: Judy H Watt-Watson, PhD, University of Toronto
• Principal Investigator: Michael H McGillion, PhD, University of Toronto

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• ClinicalTrials.gov Identifier: NCT00350922
• Other Study ID Numbers: 452639
• First Posted: Jul 11, 2006
• Last Update Posted: Jul 11, 2006
• Last Verified: Nov 1, 2005

• Additional relevant MeSH terms: Angina Pectoris; Angina, Stable

Study Results

No Results Posted as of Jul 11, 2006