- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06550661
Effects of Ba Duan Jin Training for Older People
August 3, 2025 updated by: Chiu Shu-Ching, Central Taiwan University of Science and Technology
Effects of Ba Duan Jin on Muscle Strength, Balance, Cardiorespiratory Endurance, Body Composition and Quality of Life of Older People
Baduanjin is one of the widely circulated fitness methods.
The Ministry of Health, the Ministry of Education and the General Administration of Sports of China have vigorously promoted it as one of the contents of health and physical education classes, and promoted it as a health Qigong method throughout mainland China.
It can be seen that Baduanjin's gentle and non-aggressive movements are suitable for physical training for people of all ages.
Study Overview
Study Type
Interventional
Enrollment (Actual)
78
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
-
-
-
Taichung, Taiwan
- Show Chwan Memorial Hospital
-
-
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) old person able to communicate and follow instructions, (2) stable and with sufficient physical strength: able to maintain at least one sitting position in a wheelchair or on the edge of a bed.
Exclusion Criteria:
- (1) Difficulty standing or walking and obvious musculoskeletal disease, (2) Diagnosed and recommended by a physician Those who are not suitable for sports activities, (3) serious diseases/unstable conditions, such as severe cardiopulmonary, liver and kidney diseases, severe malignant tumors, severe malnutrition, severe dementia, (4) more than 180 minutes of exercise per week in the past month time, (5) severe arrhythmia, (6) no intention to participate.
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Ba duan jin training
twice a week
|
a kind of exercise
|
|
No Intervention: usual care
once a week with video
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Chang in muscle strength from baseline to 12 weeks
Time Frame: Baseline and 12 weeks
|
pinch, grip and quadriceps strength.
A Higher score means a better outcome.
|
Baseline and 12 weeks
|
|
Chang in weight of muscle and fat from baseline to 12 weeks
Time Frame: Baseline and 12 weeks
|
muscle mass(kg/%), fat mass (kg/%)
|
Baseline and 12 weeks
|
|
Chang in Activities of Daily Living from baseline to 12 weeks
Time Frame: Baseline and 12 weeks
|
This is a scale of physical function.
The range for total score is 0-100.
A Higher score means a worse outcome.
|
Baseline and 12 weeks
|
|
Chang in Instrumental activities of daily living from baseline to 12 weeks
Time Frame: Baseline and 12 weeks
|
This is a scale of physical function.
The range for total score is 0-24.
A Higher score means a better outcome.
|
Baseline and 12 weeks
|
|
Chang in short form Berg balance scale from baseline to 12 weeks
Time Frame: Baseline and 12 weeks
|
Balance Assessment.
The range is 0-4.
A Higher score means a better outcome.
|
Baseline and 12 weeks
|
|
Chang in Gait analyses from wearable sensors from baseline to 12 weeks
Time Frame: Baseline and 12 weeks
|
MTC mean magnitude and variability, as well as the stride-to-stride variability, stride time and length, lower limb peak angular velocity, and foot forward linear speed
|
Baseline and 12 weeks
|
|
Chang in EQ5D from baseline to 12 weeks
Time Frame: Baseline and 12 weeks
|
This is a scale of quality of life.
The range for total is 0-20.
A higher score means a worse outcome.
|
Baseline and 12 weeks
|
|
Chang in WHOBREF from baseline to 12 weeks
Time Frame: Baseline and 12 weeks
|
This is a scale of quality of life.
A higher score means a better outcome.
|
Baseline and 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
age, gender, married, religion, sleep, fall, disease status, education
Time Frame: Baseline
|
Demographic basic data
|
Baseline
|
|
height, weight
Time Frame: Baseline
|
height(cm), weight(kg)
|
Baseline
|
|
Clinical Dementia Rating
Time Frame: Baseline
|
Mental Function Assessment.
The range is 0-3.
A Higher score means a worse outcome.
|
Baseline
|
|
Chang in Cumulative Illness Rating Scale
Time Frame: Baseline
|
A Higher score means a worse outcome.
Range Min and Max to 0-56.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Chiu, Central Taiwan University of Science and Technology
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 3, 2024
Primary Completion (Actual)
September 12, 2024
Study Completion (Actual)
April 30, 2025
Study Registration Dates
First Submitted
August 6, 2024
First Submitted That Met QC Criteria
August 8, 2024
First Posted (Actual)
August 13, 2024
Study Record Updates
Last Update Posted (Actual)
August 6, 2025
Last Update Submitted That Met QC Criteria
August 3, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- CTU112-SHOW-002
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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