Ireland
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Recruiting Not applicable

Effects of Baduanjin Exercise on Improving Health in Sedentary Young and Middle-Aged Adults

NCT07482995 · tracked via the Priya Life Science Japan tracker
Phase
Not applicable
Started
2026-09-30
Last updated
2026-11-05

Condition(s) studied

Sedentary LifestyleBehavioral Intervention

Investigational drug(s) / intervention(s)

Baduanjin exerciseGeneral Health Education

Baduanjin exercise: A 12-week, standardized Baduanjin exercise program. Participants will complete 5 sessions per week, each lasting 60 minutes (including warm-up, Baduanjin practice, and cool-down). The program includes both supervised group sessions and guided home practice.

General Health Education: Participants will receive general health education (including recommendations on physical activity types and duration), but will not be enrolled in any structured or supervised exercise program. They will be instructed to maintain their usual lifestyle.

Study summary

The goal of this clinical trial is to learn if a 12-week Baduanjin exercise program can improve health in sedentary young and middle-aged adults. The main questions it aims to answer are:

1. Does the Baduanjin program improve participants' cardiorespiratory fitness (measured as peak oxygen uptake)?
2. Does it improve their body composition, muscle strength, balance, and flexibility?
3. Does it reduce their daily sitting time?

Researchers will compare the Baduanjin training group to a health education control group to see if Baduanjin is more effective in improving these health outcomes.

Participants will:

1. Be randomly assigned to one of the two groups.
2. If in the Baduanjin group, attend supervised group sessions and practice at home for 12 weeks.
3. Complete a series of assessments at the beginning, middle, and end of the study, including fitness tests, body measurements, and questionnaires.

Eligibility

Sex
ALL
Min age
18 Years
Max age
59 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Adults aged 18 to 59 years * Sedentary and physically inactive, defined as: (a) self-reported sitting time ≥ 8 hours per day, AND (b) not meeting the World Health Organization (WHO) recommended level of physical activity ( engaging in \< 150 minutes of moderate-to-vigorous intensity physical activity per week, assessed by the International Physical Activity Questionnaire \[IPAQ\]) * In good general health as self-reported, and free from any known diseases * Willing and able to provide written informed consent Exclusion Criteria: * Contraindications to cardiopulmonary exercise testing * Currently participating in, or planning to participate within the next 3 months, in any other structured exercise or behavioral intervention program * Pregnancy, lactation, or planning to become pregnant during the study period * Inability to understand or comply with the study procedures

Primary outcome measure(s)

  • Change in Peak Oxygen Uptake (VO₂peak) assessed by Cardiopulmonary Exercise Testing — at baseline and Week 13.
    Measured by Cardiopulmonary Exercise Testing (CPET).

Trial sites (1)

FacilityCityRegionStatus
China-Japan Friendship Hospital Beijing Beijing Municipality Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07482995 on ClinicalTrials.gov ↗ ← All trials in Japan