Taekwondo Program for Preventing Falls in Older Adults

April 6, 2026 updated by: Chih-Hsiang Yang, University of South Carolina

Evaluating a Taekwondo-based Fall Prevention Exercise Program in Older Adults: a Feasibility Study

Falls in older adults are a public health crisis, as 30% of older adults fall each year, with a mortality rate of 78%.1 Fall-related healthcare costs are over 50 billion dollars.1 Therefore, preventing older adults from falling is important in both individual and public health aspects by increasing their quality of life and reducing healthcare costs. However, the current fall-prevention exercise programs have a limitation in maintaining exercise adherence behaviors or increasing physical activities once the intervention is completed.2 The theory-based exercise program shows a higher adherence and retention rate.3,4 Taekwondo (TKD), one type of martial arts, can be a potential channel to deliver a theory-based fall prevention exercise program. Therefore, this study aims to test the feasibility of the potential 12 Taekwondo-based fall prevention exercise program for older adults and its preliminary efficacy using a randomized controlled trial.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

20

Phase

  • Early Phase 1

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

    • South Carolina
      • Columbia, South Carolina, United States, 29201
        • University of South Carolina

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Older adults ages 55 and above
  2. Adequate physical ability to perform walking independently
  3. Able to use a smartphone app without assistance
  4. Capable of providing informed consent
  5. Agree to be randomized to the group

Exclusion Criteria:

  1. Plan to have surgery or relocate outside the area within the next 3 months
  2. Currently participate in other studies involving physical activity or fall-prevention research studies
  3. Frail older adults screened by the FRAIL questionnaire

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

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Taekwondo exercise arm
Participants will received 12 sessions of Taekwondo-based fall prevention exercises. The exercise will be delivered twice a week for 6-weeks at the local recreational center. Each sessions includes three components: static and dynamic stretching warm-up, basic Taekwondo movement exercises, and kicking exercises. Static and dynamic warm-up was developed based on the evidence-based fall prevention exercise, The Otago Exercise Program. The basic Taekwondo movement exercises include three basic stances (walking, front, and horse riding stances) , and hand movements (low, middle, and high block, and middle punch). Kicking exercise includes target kicking using front kicks.
Current fall-prevention exercise programs have a limitation in maintaining exercise adherence behaviors or increasing physical activities once the intervention is completed.2 The theory-based exercise program shows a higher adherence and retention rate.3,4 Taekwondo (TKD), one type of martial arts, can be a potential channel to deliver a theory-based fall prevention exercise program. Therefore, this study aims to test the feasibility of the potential 12 Taekwondo-based fall prevention exercise program for older adults and its preliminary efficacy using RCT.
Active Comparator: Fall prevention education arm
Participants will received the Live Strong and Safe Program on Fall Prevention online education program. It includes three modules. Module1 has three sessions that providing overview of fall prevention such as fall statistics, and preventable risk factors. Module2 has eight sessions that provides tips to ensure home safety for fall prevention. Module3 has 12 sessions that provides tips for personal safety from nutrition to mental health. Participants will complete this module at their own pace, and report their progress through email or text message each week.
Live Strong and Safe Program on Fall Prevention online education includes three modules. Module1 has three sessions that provide overview of fall prevention such as fall statistics, and preventable risk factors. Module2 has eight sessions that provide tips to ensure the home safety for fall prevention. Module3 has 12 sessions that provide tips for personal safety from nutrition to mental health. Participants will complete this module at their own pace, and report their progress through email or text message each week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Recruitment Feasibility
Time Frame: Post-intervention at week 7.
The number of participants enrolled in the study per month; The number of participants who provided consent over the eligible participants.
Post-intervention at week 7.
Intervention Satisfaction
Time Frame: Post intervention at week 7
8-item questionnaire with 7-point Likert (adapted from Physical Activity Enjoyment Scale). The response scale ranges from 1-7, spanning from the lowest degree (=1) to the highest degree (=7).
Post intervention at week 7
Perceived feasibility
Time Frame: Post intervention at week 7
Using 5 points Likert Scale, and the response scale is (1): Completely disagree; (3) Neither agree or disagree; to (5): Completely agree. These items ask about participants' perceived program acceptability, appropriateness, and feasibility
Post intervention at week 7
Intervention fidelity
Time Frame: Every exercise session
Fidelity checklist scored by the independent rater
Every exercise session
Adherence rate
Time Frame: Post intervention (At Week 7)
Number of sessions each participant attended / total sessions provided (i.e., 12)
Post intervention (At Week 7)
Intention to reparticipate
Time Frame: Post intervention (At Week 7)
Use 4-item questionnaire with 5-point Likert Scale. The response scale is (1): Strongly disagree; (3) Neither agree or disagree, to Maximum (5): Strongly agree
Post intervention (At Week 7)
Adverse event
Time Frame: Anytime during the intervention period
The number of grade 1 adverse events occurred across all exercise sessions.
Anytime during the intervention period

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical function
Time Frame: Baseline (Week 0) and post-intervention (Week 7)
Static and dynamic balance: Balance Error Scoring System (Outcome unit: number of errors occurred) Functional Gait Assessment (Outcome unit: a score ranging from 0-30) Muscle strength: 30-second chair-stand tests (Outcome unit: number of successful trials) Gait speed: Timed-Up and Go (Outcome unit: total time (seconds) to complete the task)
Baseline (Week 0) and post-intervention (Week 7)
Fear of falling
Time Frame: Baseline (Week 0) and post-intervention (Week 7)
The Falls Efficacy Scale-International - 16 items with 4-point Likert Scale ranging from (1): Not at all concerned to (4): Very concerned.
Baseline (Week 0) and post-intervention (Week 7)
Activity and Sedentary fragmentation
Time Frame: Baseline (Week 0) and post-intervention (Week 7)
Activity fragmentation: Transition probability from activity behavior to sedentary behavior every minute. Sedentary fragmentation: Transition probability from sedentary behavior to activity behavior every minute.
Baseline (Week 0) and post-intervention (Week 7)

Collaborators and Investigators

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

Investigators

  • Study Chair: Chih-Hsiang Yang, PhD, 2. University of South Carolina

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 13, 2026

Primary Completion (Estimated)

September 30, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

February 23, 2026

First Submitted That Met QC Criteria

April 6, 2026

First Posted (Actual)

April 13, 2026

Study Record Updates

Last Update Posted (Actual)

April 13, 2026

Last Update Submitted That Met QC Criteria

April 6, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Pro00137158

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The study will be conducted from a restricted area and the participants will be recruited from local senior centers, which has high risk of identifying the personal information of study participants.

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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