- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04173936
Community-based Tai Chi, Balance, and Fall Risk
Effects of a Community-based Tai Chi Program on Balance, Functional Outcomes, and Sensorimotor Function in Older Adults
Aims: Examine the effects of a community Tai Chi program on measures of balance and sensorimotor function.
Methods: In a pre-test and post-test design, balance was measured in older adults (N=344; 73.4±7.4 years) with 30-second chair stand, timed-up and go, and 4-stage balance test following a 12-week community-based tai chi intervention. Balance measures and additional sensorimotor measures, including hip abductor electromechanical delay and hip proprioception, were measured in a smaller sample of older adults (n=11; 67.3±3.7 years).
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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North Carolina
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Asheville, North Carolina, United States, 28804
- UNC Asheville
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- age 60 years or older
- ability to independently ambulate
- self-described concern with stability and/or mobility.
Exclusion Criteria:
- Neurological diagnosis
- Participants body weight exceeds >450 pounds).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Tai Chi
All participants enrolled in a 12 week community-based tai chi program.
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12-week community-based tai chi program
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
30-second chair number
Time Frame: 12 weeks
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The number of times a person can stand up and sit down from a chair in 30 seconds
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12 weeks
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Timed Up and Go
Time Frame: 12 weeks
|
The time (in seconds) for a person to stand from a chair, walk 10 feet, turn 180 degrees and return to sit in the chair
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12 weeks
|
4 stage balance test
Time Frame: 12 weeks
|
How long (in seconds) can a person stand with feet together, stand with one foot forward and to the side, stand in tandem (one foot immediately in front of the other, and stand on one foot
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12 weeks
|
Hip abductor muscle contraction time
Time Frame: 12 weeks
|
Hip abductor muscle contraction speed as measured as the time (in milliseconds) between the onset of electromyography signal and torque onset from hip muscle abduction
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12 weeks
|
Brief-Balance Evaluation System Test
Time Frame: 12 weeks
|
The bBESTest is an 8-item, clinically-based assessment measuring anticipatory postural adjustments, compensatory postural responses, sensory orientation, stability in gait, and the timed up-and-go test.
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12 weeks
|
Activities-Specific Balance Confidence Scale (ABC) scale
Time Frame: 12 weeks
|
the ABC scale assesses self-reported confidence during 16 activities related to mobility.
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12 weeks
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Hip joint proprioception error
Time Frame: 12 weeks
|
The magnitude of proprioception error was measured on the participant's dominant lower extremity with a custom-built device25,51 that allows for rotation around the axis of a semi-goniometer to measure proprioception in the transverse plane at the hip joint.
Proprioception was assessed by measuring the accuracy of actively pointing a marked line on the second toe to target angles along the semi-goniometer during two conditions, a vision condition and an occluded vision condition.
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12 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Jason R Wingert, Phd, UNC Asheville
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1373542-1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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