Microvascular Angina Clinical Trial
Official title:
The Impact of Cardiac Rehabilitation on Angina Frequency, Psychological Morbidity and Quality of Life in Women With Syndrome X
The study is designed to test the hypothesis that participation in a standard phase III group based cardiac rehabilitation programme will improve psychological morbidity, quality of life and cardiovascular risk factors, along with chest pain severity and frequency in women with cardiac syndrome X.
Status | Completed |
Enrollment | 64 |
Est. completion date | May 2005 |
Est. primary completion date | May 2005 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 30 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Women - Aged 30 to 80 years - Postmenopausal > 1 year since last menstrual period - Angiographically normal coronary arteries - Positive treadmill exercise test for myocardial ischemia - Reported angina pectoris > 2 episodes per week - Diagnosis > 6 months - Willing to give written informed consent Exclusion Criteria: - History of psychiatric illness - History of any other chronic illness - Participation in another research study within the previous 60 days - Suffer any physical condition for which exercise is a contra-indication. - Unwilling to give written informed consent |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United Kingdom | National Heart and Lung Institute, Imperial College London | London |
Lead Sponsor | Collaborator |
---|---|
National Heart and Lung Institute | Royal Brompton & Harefield NHS Foundation Trust |
United Kingdom,
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* Note: There are 31 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Anxiety | Measured at baseline then every 8 weeks for 16 weeks | No | |
Primary | Depression | Measured at baseline then every 8 weeks for 16 weeks | No | |
Primary | Health anxiety | Measured at baseline then every 8 weeks for 16 weeks | No | |
Primary | Cardiac anxiety | Measured at baseline then every 8 weeks for 16 weeks | No | |
Primary | Quality of life | Measured at baseline then every 8 weeks for 16 weeks | No | |
Primary | Symptom severity | Measured at baseline then continuously for 16 weeks | Yes | |
Primary | Symptom frequency | Measured at baseline then continuously for 16 weeks | Yes | |
Secondary | Cardiovascular risk factors | Measured at baseline, 8 weeks and 16 weeks. | No | |
Secondary | Physical ability | Baseline and at 8 weeks | No | |
Secondary | Time to pain | Baseline and 8 weeks | No |
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