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Multicenter Clinical Investigation on the Effectiveness of Machine Learning-Based Multimodal Features of Cardiac and Cerebral Electrophysiology in Auxiliary Diagnosis of Adolescent Depressive Disorder

Multicenter Clinical Investigation on the Effectiveness of Machine Learning-Based Multimodal Features of Cardiac and Cerebral Electrophysiology in Auxiliary Diagnosis of Adolescent Depressive Disorder

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125566
Enrollment
Unknown
Registered
2026-05-28
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

major depressive disorder

Interventions

Healthy Control Group:None

Sponsors

The First Affiliated Hospital of University of South China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. DD Group (Depressive Disorder Group): (1) Aged 12–18 years, male or female. (2) Meet the diagnostic criteria for depressive disorder according to DSM-5, with a total score of =7 on the 17-item Hamilton Depression Rating Scale (HAMD-17). (3) The patient voluntarily participates in this study, and both the patient and their legal guardian have signed the written informed consent form. 2. HC Group (Healthy Control Group): (1) Aged 12–18 years, male or female. (2) Total score <7 on the 17-item Hamilton Depression Rating Scale (HAMD-17). (3) No prior history of any mental illness. (4) The subject voluntarily participates in this study, and both the subject and their legal guardian have signed the written informed consent form.

Exclusion criteria

Exclusion criteria: (1) Presence of severe physical illness. (2) Previous history of mental illness. (3) Presence of cognitive impairment, hearing, visual, or intellectual disabilities that prevent cooperation in completing the 17-item Hamilton Depression Rating Scale (HAMD-17) assessment. (4) Women who are pregnant or breastfeeding. (5) Individuals with drug abuse or alcohol dependence. (6) Participation in a related clinical trial within the past 3 months. (7) Any other conditions that, in the investigator's opinion, make the subject unsuitable for participation in the clinical study.

Design outcomes

Primary

MeasureTime frame
17-Item Hamilton Depression Rating Scale Score;electrocardiogram;electroencephalogram;systolic blood pressure;diastolic blood pressure;heart rate;

Countries

China

Contacts

Public ContactHuifang Tang

The First Affiliated Hospital of University of South China

tanghuifang999@163.com+86 135 4850 5158

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026