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To study the clinical effect of Baduanjin combined with five-tone therapy on liver stagnation and spleen deficiency depression based on infrared heat map

To study the clinical effect of Baduanjin combined with five-tone therapy on liver stagnation and spleen deficiency depression based on infrared heat map

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086471
Enrollment
Unknown
Registered
2024-07-02
Start date
2024-07-02
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Depression

Interventions

Intervention group:Basic treatment (Sertraline hydrochloride tablets + Shugan Jieyu capsules) + Baduanjin + Wuyin therapy
Control group:Basic treatment (Sertraline hydrochloride tablets + Shugan Jieyu capsules)

Sponsors

Tsinghua University Yuquan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for "Yu's disease" (liver qi stagnation and spleen deficiency syndrome) in traditional Chinese medicine; (2) Meet the diagnostic criteria for mild to moderate depressive episode according to Western medicine; (3) HAMD-17 score > 17 points, and Hamilton Anxiety Scale (HAMA) score < 7 points; (4) Participants aged 18 years or older and under 70 years of age; (5) Without other serious somatic diseases or psychological disorders; (6) Completed questionnaires and other relevant clinical data; (7) Participants who are conscious and willing to participate in the study and sign informed consent forms. Anyone who meets the above criteria can be included.

Exclusion criteria

Exclusion criteria: (1) Individuals with a history or present tendency towards suicide and/or suicide attempts; (2) Individuals with serious or chronic diseases of the heart, brain, lungs, liver, kidneys, or blood system, or patients with mental illness; (3) Individuals with a history of alcohol or drug abuse; (4) Individuals whose questionnaires are incomplete or whose relevant clinical information is incomplete; (5) Individuals who do not agree to participate in this study. Individuals who meet any of the above criteria will be excluded.

Design outcomes

Primary

MeasureTime frame
Effective rate of disease treatment;

Secondary

MeasureTime frame
Heat value data of infrared heat map;

Countries

China

Contacts

Public ContactQingjie Yuan

Tsinghua University Yuquan Hospital

yuanqingjiedf@163.com+86 188 1046 5989

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026