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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01007903
Other study ID # 2007P000065
Secondary ID
Status Completed
Phase Phase 1
First received November 3, 2009
Last updated February 23, 2017

Study information

Verified date February 2017
Source Beth Israel Deaconess Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 45 Years and older
Eligibility Inclusion Criteria:

- physician diagnosis of COPD

- FEV1<65% of predicted and FEV1/FVC<0.70

- =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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Tai Chi exercise
12-week tai chi exercise class

Locations

Country Name City State
United States Beth Israel Deaconess Medical Center Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Beth Israel Deaconess Medical Center National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Study feasibility
Secondary Quality of life
Secondary Exercise capacity
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