Community-based Tai Chi, Balance, and Fall Risk

Sponsor
University of North Carolina at Asheville (Other)
Overall Status
Completed
CT.gov ID
NCT04173936
Collaborator
(none)
405
1
41.1
9.9

Study Details

Study Description

Brief Summary

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).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: tai chi

Study Design

Study Type:
Observational
Actual Enrollment :
405 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Effects of a Community-based Tai Chi Program on Balance, Functional Outcomes, and Sensorimotor Function in Older Adults
Actual Study Start Date :
Jan 11, 2014
Actual Primary Completion Date :
Jun 15, 2017
Actual Study Completion Date :
Jun 15, 2017

Arms and Interventions

Arm Intervention/Treatment
Tai Chi

All participants enrolled in a 12 week community-based tai chi program.

Behavioral: tai chi
12-week community-based tai chi program

Outcome Measures

Primary Outcome Measures

  1. 30-second chair number [12 weeks]

    The number of times a person can stand up and sit down from a chair in 30 seconds

  2. Timed Up and Go [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

  3. 4 stage balance test [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

  4. Hip abductor muscle contraction time [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

  5. Brief-Balance Evaluation System Test [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.

  6. Activities-Specific Balance Confidence Scale (ABC) scale [12 weeks]

    the ABC scale assesses self-reported confidence during 16 activities related to mobility.

  7. Hip joint proprioception error [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years to 95 Years
Sexes Eligible for Study:
All
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).

Contacts and Locations

Locations

Site City State Country Postal Code
1 UNC Asheville Asheville North Carolina United States 28804

Sponsors and Collaborators

  • University of North Carolina at Asheville

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of North Carolina at Asheville
ClinicalTrials.gov Identifier:
NCT04173936
Other Study ID Numbers:
  • 1373542-1
First Posted:
Nov 22, 2019
Last Update Posted:
Nov 22, 2019
Last Verified:
Nov 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 22, 2019