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Clinical Trials/NCT02287740
NCT02287740
Completed
Not Applicable

Comparative Effectiveness and Cost-effectiveness of a Fall Prevention Intervention: Tai Ji Quan: Moving for Better Balance

Oregon Research Institute1 site in 1 country670 target enrollmentNovember 2014
ConditionsFall

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fall
Sponsor
Oregon Research Institute
Enrollment
670
Locations
1
Primary Endpoint
Change in the number of falls
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Objective: To conduct a comparative efficacy and cost-effectiveness study of an evidence-based fall prevention program-Tai Ji Quan: Moving for Better Balance (TJQMBB).

Detailed Description

To determine the effectiveness and cost-effectiveness of the two evidence-based exercise programs (Multimodal Exercise,TJQMBB) relative to stretching, a proxy for a minimum practice standard, in reducing falls among older adults at risk of falling.

Registry
clinicaltrials.gov
Start Date
November 2014
End Date
March 30, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • aged 70 years or older living independently in the community
  • at least one fall in the preceding 12 months and a referral from a healthcare provider indicating the participant is at risk of falls due to gait/balance impairment or medication use or impaired mobility as evidenced by Timed Up and Go result of \>13.5 seconds
  • no participation in daily and/or structured vigorous physical activity or walking for exercise that lasted 15 minutes or longer at a time or muscle-strengthening activities on 2 or more days a week in the previous 3 months
  • walking independently, with or without the use of an assistive device,
  • no severe cognitive impairment (Mini-Mental State Examination score ≥20)
  • able to exercise safely as determined by their healthcare provider,
  • a willingness to be randomly assigned to an intervention condition and complete the 6-month intervention and 6 month follow-up.

Exclusion Criteria

  • any medical or physical conditions deemed unacceptable by their physician or healthcare provider,
  • planned to leave the study area within the next 12 months.

Outcomes

Primary Outcomes

Change in the number of falls

Time Frame: Baseline, 6 Months

Using a daily diary "fall calendar," falls reported by participants across the 24-week surveillance period will be collected, starting from the date of first intervention class and continuing until participants withdrew, had died or were lost to follow-up.

Secondary Outcomes

  • Functional Reach(Baseline, 6 Months)
  • Cost per fall prevented(Baseline, 6 Months)
  • Instrumented Timed Up and Go(Baseline, 6 Months)
  • Physical Performance(Baseline, 6 Months)
  • Cognitive function(Baseline, 6 Months)

Study Sites (1)

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