Yoga for Treating Shortness of Breath in Chronic Obstructive Pulmonary Disease (COPD)
Efficacy of Yoga for Self-Management of Dyspnea in COPD
1 other identifier
interventional
36
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_1
Started Jan 2003
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2003
CompletedFirst Submitted
Initial submission to the registry
January 16, 2003
CompletedFirst Posted
Study publicly available on registry
January 17, 2003
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2004
CompletedAugust 18, 2006
August 1, 2006
January 16, 2003
August 16, 2006
Conditions
Interventions
Eligibility Criteria
You may qualify if:
- Able to commit to a 12-week yoga class in San Francisco, California
- Moderate to severe COPD, clinically stable for at least 1 month prior to study entry
- Forced Expiratory Volume at one minute (FEV1) \< 49% predicted after inhaled bronchodilator
- Activities of daily living limited by shortness of breath
- Ability to speak English and sign consent
- Patients receiving supplemental oxygen will be acceptable if their O2 saturation can be maintained at \> 85% on \< 6 L/min of nasal oxygen
You may not qualify if:
- Symptomatic illness (e.g., cancer, left heart failure, ischemic heart disease, neuromuscular disease, psychiatric illness)
- Formal pulmonary rehabilitation training within 1 year prior to study entry
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of California
San Francisco, California, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Virginia Carrieri-Kohlman, RN, DNSc
University of California, San Francisco
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- NIH
Study Record Dates
First Submitted
January 16, 2003
First Posted
January 17, 2003
Study Start
January 1, 2003
Study Completion
July 1, 2004
Last Updated
August 18, 2006
Record last verified: 2006-08