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Effects of Qigong, Tai Chi and Yoga Practice in Older Adults

Effects of Qigong, Tai Chi and Yog Practice on Indicators of Health and Quality of Life in Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00710853
Enrollment
50
Registered
2008-07-04
Start date
2008-05-31
Completion date
2009-06-30
Last updated
2009-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Geriatric, Qi gong, Yoga, Tai chi, Geriatric Assessment

Brief summary

The purpose of this study is to compare the effects of an 8-week intervention using YiRen Qigong, Tai Chi or Hatha yoga in older adults (age 70 and above) residing at a Gencare senior living facility. Outcome measures completed at the beginning and end of each intervention period will be blood pressure, heart rate, perceived quality of life (PQOL)and a symptoms questionnaire (SF-36), ability and speed of walking 20 feet (for ambulatory participants), and neck and arm range of motion.

Interventions

OTHERYiRen Qi gong

One hour weekly class for 8 week duration

OTHERTai Chi

One hour weekly class for 8 week duration

OTHERHatha yoga

One hour weekly class for 8 week duration

Sponsors

Gencare Incorporated
CollaboratorINDUSTRY
Bastyr University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Be a resident of a Gencare Senior Living facility in Granite Falls, Lynnwood, Renton, Ballard and Lake City, WA * Be at least 70 years of age * Be willing to participate in the tai chi, qi gong and/or yoga classes * Willing to complete study-related outcomes assessments

Exclusion criteria

* Not medically able to participate in the mild level of activity involved in the 3 interventions as determined by the resident's physician * Unable to complete study questionnaires or study procedures at screening

Design outcomes

Primary

MeasureTime frame
Blood pressureEnd of 8-week class
Heart rateEnd of 8-week class
Quality of life (SF-36 and PQOL)End of 8-week class

Secondary

MeasureTime frame
Adverse eventsEnd of 8-week class

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026