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Clinical efficacy and mechanism study of Daoyin exercise based on Zhu Bing Yuan Hou Lun intervention for anxiety and depressive states among college students

Clinical efficacy and mechanism study of Daoyin exercise based on Zhu Bing Yuan Hou Lun intervention for anxiety and depressive states among college students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001737
Enrollment
Unknown
Registered
2026-07-13
Start date
2026-07-31
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Anxiety and depressive states

Interventions

Experimental group:Mental health education plus Daoyin exercise derived from Zhu Bing Yuan Hou Lun
healthy control group:no intervention

Sponsors

Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1.College students aged 18-35 years, of either sex, and right-handed; 2.Participants with anxiety or depressive states (8 = HAMA-14 < 29 and 8 = HAMD-17 < 24); 3.Good compliance, voluntary participation in this study, willingness to cooperate with the study procedures, and signed informed consent

Exclusion criteria

Exclusion criteria: 1.Diagnosed with a severe mental/psychiatric disorder (e.g., severe anxiety disorder, severe depressive disorder, bipolar disorder, schizophrenia, personality disorder, mood disorder, obsessive-compulsive disorder [OCD], eating disorder, organic brain disorder, etc.). 2.History of alcohol/substance dependence or abuse within the past year, or currently taking psychotropic medications. 3.Presence of severe depression and suicidal ideation/risk. 4.Suffering from severe cardiopulmonary disease, musculoskeletal injury, or other physical conditions that contraindicate exercise intervention. 4.Scalp injury or infection (which would interfere with the fitting of the optode cap and data acquisition). 5.Concurrently participating in another clinical study during the same period

Design outcomes

Primary

MeasureTime frame
Outcome Name: Change in Hamilton Anxiety Rating Scale (HAMA-14) score;Outcome Name: Change in Hamilton Depression Rating Scale (HAMD-17) score;

Secondary

MeasureTime frame
Outcome Name: Changes in sleep quality, perceived stress, general well-being, and self-reported depressive symptoms;

Countries

China

Contacts

Public ContactLi Yunxin

Shanghai University of Traditional Chinese Medicine

xinzj28@163.com13589946337

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026