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Research on the Effect of Depression Evaluation-Intervention-Health Promotion Based on Physical Examination Population

Research on the Effect of Depression Evaluation-Intervention-Health Promotion Based on Physical Examination Population

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061026
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

Subthreshold Depression

Interventions

subthreshold depression intervention group:health education/Internet-based Cognitive Behavioral Therapy
subthreshold depression control group:none

Sponsors

Peking University Sixth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Depression group (1) Aged 18-65 years; (2) Diagnosed as first-episode or recurrent depressive episode according to ICD-10; (3) Voluntarily participate and sign informed consent. 2. Subthreshold depression group (1) Aged 18-65 years; (2) Subthreshold depression determined according to MINI5.0, with any two to three symptoms, and does not meet the diagnostic criteria for depression; (3) Voluntarily signed informed consent. 3. Healthy control group (1) Aged 18-65 years; (2) Have one or no symptoms; (3) HAMD-17 < 8 points, PHQ-9 < 5 points, GAD-7 < 5 points; (4) No history of mental illness; (5) Voluntarily signed informed consent Book.

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding women, patients who are unwilling to take contraceptive measures during the study period; 2. Patients with severe or unstable diseases who are judged unsuitable for participation in this study by the researchers; 3. Patients with history of serious neurological diseases (including epilepsy, seizures, brain injury, multiple sclerosis, degenerative diseases such as acute lateral sclerosis, Parkinson's disease and ataxia).

Design outcomes

Primary

MeasureTime frame
SDS deduction rate;Kappa vale;Sensitivity;specificity;Youden Index;Receiver operator characteristic curve;

Secondary

MeasureTime frame
Knowledge awareness rate;positive predictive value;

Countries

China

Contacts

Public ContactDong Wentian

Peking University Sixth Hospital

dongwentian@126.com+86 13001186672

Outcome results

None listed

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