Yoga for Treating Shortness of Breath in Chronic Obstructive Pulmonary Disease (COPD)

NCT ID: NCT00051792

Last Updated: 2006-08-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1/PHASE2

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-01-31

Study Completion Date

2004-07-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Pulmonary Disease, Chronic Obstructive Lung Diseases, Obstructive Pulmonary Emphysema Chronic Bronchitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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yoga

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* 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
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Center for Complementary and Integrative Health (NCCIH)

NIH

Sponsor Role lead

Principal Investigators

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Virginia Carrieri-Kohlman, RN, DNSc

Role: PRINCIPAL_INVESTIGATOR

University of California, San Francisco

Locations

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University of California

San Francisco, California, United States

Site Status

Countries

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United States

Other Identifiers

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R21AT001168-01

Identifier Type: NIH

Identifier Source: org_study_id

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