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

Status

Completed

Conditions

Intervention / Treatment

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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