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Study on Individual and Group Intervention Models of Yishu psychodrama Technology in the Treatment and Rehabilitation of Outpatient Depression

Study on Individual and Group Intervention Models of Yishu psychodrama Technology in the Treatment and Rehabilitation of Outpatient Depression

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071340
Enrollment
Unknown
Registered
2023-05-11
Start date
2019-01-15
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Depression

Interventions

Observation group:Yi Shu psychodrama treatment
Control group:first-line antidepressant (escitalopram oxalate) treatment

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Meeting the diagnostic criteria for single-phase depressive episodes in the tenth edition of the International Classification of Diseases (ICD-10), with a score of 5<BDI-13<16 (2) Junior high school or above education level (3) Never taken antidepressants before or withdrawal of more than a month (4) Ability to cooperate with pre-enrollment physical examinations, understand and cooperate with questionnaire filling, cranial fMRI, etc. (5)18.5=BMI<24kg/m2 (6) Voluntary participation and signing the consent inform

Exclusion criteria

Exclusion criteria: (1) Organic brain diseases and imaging data that are not qualified (2) Merging other mental illnesses, including persistent depressive episodes with psychotic symptoms, bipolar depression, post-traumatic stress disorder, and severe personality disorders (such as borderline personality) (3) Severe physical diseases, including hypertension, diabetes, coronary heart disease, thyroid disease, etc (4) Alcohol or substance dependence (5) Serious suicidal ideation, self-injurious behavior and suicide attempt (6) Electroconvulsive therapy within 6 months or other systemic psychotherapy or transcranial magnetic therapy (7) Major surgery within 3 months or history of cold and fever symptom within 2 weeks (8) Patients receiving glucocorticoid therapy (9) Pregnant or lactating women (10) Left-handedness (11) Having contraindication of MRI scanning, unable to complete MRI scanning or be alone in confined space for 1h (12) Diagnosis of other sleep disorders such as apnea syndrome

Design outcomes

Primary

MeasureTime frame
Beck Depression Inventory-13 Item;Beck Anxiety Inventory-21 Item;Automatic Thoughts Questionnaire;Connor Davidson Resilience Scale;Self-Esteem Scale;Cognitive Emotion Regulation Questionnaire Chinese Version ;Simplified Coping Style Questionnaire;Temporal Experience of Pleasure Scale;adult attachment scale;Pittsburgh sleep quality index;

Countries

China

Contacts

Public ContactHua Hu

The First Affiliated Hospital of Chongqing Medical University

594550751@qq.com+86 186 2318 6901

Outcome results

None listed

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