Skip to content

Baduanjin Alleviates Chronic Stress in Military Personnel: Evidence from Subjective Reports to Objective Biomarkers and Cognitive Function

Baduanjin Alleviates Chronic Stress in Military Personnel: Evidence from Subjective Reports to Objective Biomarkers and Cognitive Function

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000285
Enrollment
Unknown
Registered
2026-02-03
Start date
2025-06-22
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Stress

Interventions

Positive Control Group:24-Form Simplified Tai Chi
Wait-List Control Group:They maintained their original daily lifestyle and received Baduanjin training guidance as compensation upon completion of the study.

Sponsors

No. 36, Jinqiansong East Road, Sujiatun District, Shenyang City, Liaoning Province, China
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Active-duty military personnel, aged 18 years or older; (2) Meeting the diagnostic criteria for chronic stress according to the ICD-11 (International Classification of Diseases, 11th Revision) [23] and relevant Chinese standards [24,25], and scoring = 43 points on the 14-item Perceived Stress Scale (PSS-14) (indicating high to very high perceived stress); (3) Being fully conscious, possessing normal communication skills, and able to cooperate in completing questionnaires; (4) Having been informed about the study and voluntarily agreeing to participate in the survey; (5) Not having undergone any other therapies beneficial to physical and mental rehabilitation (e.g., psychotherapy, yoga, Tai Chi, Qigong, sandplay, art therapy, etc.) in the past three months.

Exclusion criteria

Exclusion criteria: (1) Presence of contraindications to exercise (e.g., severe cardiovascular disease, bone/joint injuries, etc.); (2) Currently receiving psychotherapy or taking psychotropic medications; (3) Recent experience of major psychological trauma (e.g., bereavement, etc.); (4) Severe physical disabilities or mental disorders; (5) Participation in other research trials within the past three months that may affect the outcomes of this study; (6) Unwillingness to comply with the survey procedures or demonstrating a tendency of non-cooperation.

Design outcomes

Primary

MeasureTime frame
Chronic Stress;

Secondary

MeasureTime frame
Anxiety ;Depression;Human Salivary Cortisol (SC);Human Dehydroepiandrosterone (DHEA);Human C-Reactive Protein (CRP);Human Testosterone (T);

Countries

China

Contacts

Public ContactFeilong Wu

Department of Military Medical Psychology, Air Force Medical University

201607025@xaau.edu.cn18220872017

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026