- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07629622
Tai-Chi Chuan and Frenkel Coordination Exercises in Elderly
June 1, 2026 updated by: Halic University
Investigation of the Short-Term Effects of Tai-Chi Chuan and Frenkel Coordination Exercises on Balance, Coordination, and Kinesiophobia in Healthy Elderly: A Randomised Controlled Trial
This study was aimed to investigated the short-term effects of Tai-Chi Chuan (TCC) and Frenkel Coordination Exercises (FCE) on balance, coordination, and kinesiophobia in elderly.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Participants were randomly divided into two groups: [Grup 1: TCC (n=15); Grup 2: FCE (n=15)].
Balance was assessed using test Four Square Step Test (FSST), coordination using test Plate Taping Test (PTT), and kinesiophobia using test Tampa Scale of Kinesiophobia (TSK).
Although there were a statistically significant difference in all parameters in both groups (p<0,05), there was significant difference between the groups (p>0,05).
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
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
-
-
-
Istanbul, Turkey (Türkiye)
- Halic Universiy
-
-
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
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- being between 65-74 years of age;
- being able to move without the need for an assistive device;
- having a Mini Mental State Examination (MMSE) score ≥24
Exclusion Criteria:
- having a serious systemic illness that would limit participation in low-to-moderate intensity exercise,
- having been involved in any exercise program within the last three months;
- having suffered a fracture due to balance problems within the six months prior to study.
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group 1
Tai-Chi Chuan (TCC)
|
The Tai Chi-10 form, which is easy to learn and apply, was preferred, since our population consisted of elderly.
The practice was performed only for participants in Group 1, twice a week for four weeks.
|
|
Experimental: Group 2
Frenkel Coordination Exercises (FCE)
|
The practice was performed only for participants in Group 2, twice a week for four weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Four Square Step Test (FSST)
Time Frame: at baseline and at week 4
|
Four Square Step Test (FSST), which has undergone validity and reliability studies, was used for balance assessment in elderly
|
at baseline and at week 4
|
|
Plate Taping Test (PTT)
Time Frame: at baseline and at week 4
|
Plate Taping Test (PTT) was used to assess coordination skills in elderly.
|
at baseline and at week 4
|
|
Tampa Scale of Kinesiophobia (TSK)
Time Frame: at baseline and at week 4
|
Tampa Scale of Kinesiophobia (TSK), for which Turkish validity and reliability studies have been conducted, was used to assess kinesiophobia in elderly
|
at baseline and at week 4
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Aysenur Cetinkaya, PT, PhD, Halic University
- Principal Investigator: Irem Cetinkaya, PT, PhD, Halic University
- Principal Investigator: Dilek Sahinoglu, PT, PhD, Halic Universitty
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.
Helpful Links
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)
May 1, 2025
Primary Completion (Actual)
May 30, 2025
Study Completion (Actual)
March 1, 2026
Study Registration Dates
First Submitted
June 1, 2026
First Submitted That Met QC Criteria
June 1, 2026
First Posted (Actual)
June 5, 2026
Study Record Updates
Last Update Posted (Actual)
June 5, 2026
Last Update Submitted That Met QC Criteria
June 1, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 300526
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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