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| Sponsored by: |
National Center for Complementary and Alternative Medicine (NCCAM) |
| Information provided by: | National Center for Complementary and Alternative Medicine (NCCAM) |
| ClinicalTrials.gov Identifier: | NCT00051792 |
Purpose
The purpose of this study is to evaluate the safety and effectiveness of yoga in reducing shortness of breath in people with chronic obstructive pulmonary disease (COPD). Patients in this study must have moderate to severe COPD and be primarily limited by shortness of breath.
| Condition | Intervention | Phase |
|
Pulmonary Disease, Chronic Obstructive Lung Diseases, Obstructive Pulmonary Emphysema Chronic Bronchitis |
Behavioral: yoga |
Phase I Phase II |
| Genetics Home Reference related topics: | Emphysema |
| MedlinePlus related topics: | Bronchitis COPD (Chronic Obstructive Pulmonary Disease) Emphysema |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | Efficacy of Yoga for Self-Management of Dyspnea in COPD |
| Estimated Enrollment: | 36 |
| Study Start Date: | January 2003 |
| Estimated Study Completion Date: | July 2004 |
Management of dyspnea (shortness of breath) is a major concern for patients with COPD. The efficacy of complementary exercises to manage dyspnea is unknown. Complementary exercises may be more congruent with patients' lifestyles and values than traditional exercise programs and can be adapted to changes in illness severity and disability. Yoga practice is a complementary therapy that people use to manage their dyspnea. The aims of this study are to: 1) develop a safe and feasible yoga program for patients with COPD; 2) test the efficacy of this program; and 3) determine whether physical performance, psychological well being, and health-related quality of life are positively affected by yoga practice.
Patients in this study will be randomized to receive yoga training or usual care for 12 weeks. Patients will be evaluated at study entry, after each session, and immediately after the training program.
Eligibility
| Ages Eligible for Study: | 40 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion criteria:
Exclusion criteria:
Contacts and Locations| United States, California | |||||
| University of California | |||||
| San Francisco, California, United States | |||||
| Principal Investigator: | Virginia Carrieri-Kohlman, RN, DNSc | University of California, San Francisco |
More Information
| Study ID Numbers: | R21 AT001168-01 |
| First Received: | January 16, 2003 |
| Last Updated: | August 16, 2006 |
| ClinicalTrials.gov Identifier: | NCT00051792 |
| Health Authority: | United States: Federal Government |
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