Effects of Tai Chi on Frailty in Elderly Adults
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ClinicalTrials.gov Identifier: NCT01126723 |
Recruitment Status :
Completed
First Posted : May 20, 2010
Results First Posted : January 30, 2015
Last Update Posted : February 23, 2015
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Frailty | Other: Tai Chi Other: Education-Control | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 66 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | The Effects of Tai Chi on the Nonlinear Dynamics of Frailty in Elderly Adults |
Study Start Date : | September 2010 |
Actual Primary Completion Date : | September 2013 |
Actual Study Completion Date : | September 2013 |
Arm | Intervention/treatment |
---|---|
Experimental: Tai Chi group |
Other: Tai Chi
The Tai Chi intervention will consist of a 12 week, instructor-led, group-based Tai Chi training program (two, one-hour sessions per week). |
Active Comparator: Educational Control group |
Other: Education-Control
The Education-Control intervention consists of a 12 week, instructor-led attention control program consisting of health education and mind-body breathing exercises (two, one-hour sessions per week) |
- Frailty Index [ Time Frame: post-intervention ]Frailty is defined as the combination of unintentional weight loss, exhaustion, low physical activity, slow walking speed, and muscular weakness.

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Ages Eligible for Study: | 70 Years and older (Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Men and women over age 70 will be included if they are able to stand and walk unassisted, are free of any acute or unstable medical conditions, and are able to understand directions and participate in the protocol.
Exclusion Criteria:
- Potential subjects will be excluded 1) if they cannot stand and ambulate unassisted, 2) are experiencing any symptomatic cardiovascular or respiratory disease, or have 3) a myocardial infarction or stroke within 6 months, 4) painful arthritis, spinal stenosis, amputation, painful foot lesions, or neuropathy that limits balance and mobility, 5) systolic BP above 160 or diastolic BP above 100 mm Hg, 6) a cardiac pacemaker, 7) Parkinson's Disease or other neuromuscular disorder, 8) metastatic cancer or immunosuppressive therapy, or 9) have significant visual impairment.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01126723
United States, Massachusetts | |
Hebrew Rehabilitation Center | |
Roslindale, Massachusetts, United States, 02131 |
Principal Investigator: | Lewis Lipsitz, MD | Hebrew Rehabilitation Center |
Responsible Party: | Hebrew SeniorLife |
ClinicalTrials.gov Identifier: | NCT01126723 |
Other Study ID Numbers: |
10-005 R37AG025037 ( U.S. NIH Grant/Contract ) |
First Posted: | May 20, 2010 Key Record Dates |
Results First Posted: | January 30, 2015 |
Last Update Posted: | February 23, 2015 |
Last Verified: | February 2015 |
Frailty Pathologic Processes |