Community-based Tai Chi, Balance, and Fall Risk

November 21, 2019 updated by: University of North Carolina at Asheville

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

Completed

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

405

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • North Carolina
      • Asheville, North Carolina, United States, 28804
        • UNC Asheville

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

60 years to 95 years (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Older adult volunteers willing to participate in a 12-week community-based tai chi program

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
12-week community-based tai chi program

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
30-second chair number
Time Frame: 12 weeks
The number of times a person can stand up and sit down from a chair in 30 seconds
12 weeks
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
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
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
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.
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.
12 weeks
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.
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jason R Wingert, Phd, UNC Asheville

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 11, 2014

Primary Completion (Actual)

June 15, 2017

Study Completion (Actual)

June 15, 2017

Study Registration Dates

First Submitted

November 18, 2019

First Submitted That Met QC Criteria

November 21, 2019

First Posted (Actual)

November 22, 2019

Study Record Updates

Last Update Posted (Actual)

November 22, 2019

Last Update Submitted That Met QC Criteria

November 21, 2019

Last Verified

November 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 1373542-1

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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