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NCT01006447 Clinical Trial

Tai Chi/Qigong Exercise Persistence Among Residents of Senior Housing

Physical Activity Clinical Trial

Official title:
Tai Chi/Qigong Exercise Persistence Among Residents of Senior Housing: a Randomized Field Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01006447
Other study ID # DYC-023
Secondary ID
Status Completed
Phase Phase 1
First received November 1, 2009
Last updated November 1, 2009
Start date August 2009
Est. completion date October 2009

Study information
Verified date November 2009
Source D'Youville College
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This randomized field trial uses a self-report daily exercise log to answer the research question: Does frequency of instruction influence tai chi/qigong home practice exercise persistence among residents of Senior housing?

Recruitment information / eligibility
Status Completed
Enrollment 77
Est. completion date October 2009
Est. primary completion date October 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Resident of Senior housing,

- Ability to engage in mild exercise

- Vision sufficient to view TV medium

- Willingness to engage in tai chi/qigong training and practice.

Exclusion Criteria:

- Unable to provide informed consent

- Unable to attend initial training session

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

Intervention

Behavioral:
• Instructor contact

• Instructor contact

Locations
Country Name City State
United States D'Youville College Buffalo New York
United States People, Inc Senior Housing Buildings Williamsville New York

Sponsors (3)
Lead Sponsor Collaborator
D'Youville College Community Health Foundation Western NY, People. Inc

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary exercise persistence 3 months No
Secondary perceived benefits 3 months No
Secondary barriers to exercise 3 months Yes
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