Tai Chi Exercise in Patients With COPD

Tai Chi Exercise in Patients With Chronic Obstructive Pulmonary Disease

This is a pilot randomized controlled trial of feasibililty and prelimnary effects of a 12 week tai chi intervention vs. usual care in patients with chronic obstructive pulmonary disease

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Massachusetts
      • Boston, Massachusetts, United States, 02215
        • Beth Israel Deaconess Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

45 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • physician diagnosis of COPD
  • FEV1<65% of predicted and FEV1/FVC<70% of predicted
  • ≥45 years old

Exclusion Criteria:

  • COPD exacerbation requiring ER visit or hospitalization within past month
  • planned major pulmonary intervention in coming 3 months
  • severe peripheral vascular disease/claudication or other physical condition precluding walk test
  • inability to perform bicycle ergometry
  • severe cognitive dysfunction (MMSE ≤ 24)
  • inability to speak English
  • current participation in a pulmonary rehabilitation or regular practice of tai chi

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Usual Care
Experimental: Tai Chi Exercise

What is the study measuring?

Primary Outcome Measures

Outcome Measure
study feasibility

Secondary Outcome Measures

Outcome Measure
quality of life
exercise capacity

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gloria Y Yeh, MD, MPH, Beth Israel Deaconess Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

First Submitted

December 4, 2009

First Submitted That Met QC Criteria

December 4, 2009

First Posted (Estimate)

December 7, 2009

Study Record Updates

Last Update Posted (Estimate)

December 7, 2009

Last Update Submitted That Met QC Criteria

December 4, 2009

Last Verified

December 1, 2009

More Information

Terms related to this study

Other Study ID Numbers

  • K24AT000589 (U.S. NIH Grant/Contract)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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