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

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified November 2005 by University of Toronto.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00350922
First Posted: July 11, 2006
Last Update Posted: July 11, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of Toronto
  Purpose
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 Intervention Phase
Chronic Stable Angina Behavioral: Psychoeducation Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Psychoeducation Trial for People With Chronic Stable Angina

Resource links provided by NLM:


Further study details as provided by University of Toronto:

Primary Outcome Measures:
  • SF36
  • Seattle Angina Questionnaire

Secondary Outcome Measures:
  • Self-Efficacy Scale
  • Self-Control Schedule

Estimated Enrollment: 130
Study Start Date: September 2003
Estimated Study Completion Date: November 2005
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
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 -

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00350922


Locations
Canada, Ontario
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
  More Information

ClinicalTrials.gov Identifier: NCT00350922     History of Changes
Other Study ID Numbers: 452639
First Submitted: July 8, 2006
First Posted: July 11, 2006
Last Update Posted: July 11, 2006
Last Verified: November 2005

Additional relevant MeSH terms:
Angina Pectoris
Angina, Stable
Chest Pain
Pain
Neurologic Manifestations
Nervous System Diseases
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases
Signs and Symptoms