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Research on Auxiliary Diagnosis of Adolescent Depression Based on Speech Emotion Recognition Screening and Biological Indicators

Research on Auxiliary Diagnosis of Adolescent Depression Based on Speech Emotion Recognition Screening and Biological Indicators

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125284
Enrollment
Unknown
Registered
2026-05-25
Start date
2025-04-26
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

Adolescents

Interventions

Adolescent major depressive disorder group (MDD):None
Adolescent major depressive disorder with suicidal behavior group (MDDSA):None

Sponsors

The Second People's Hospital Of Taizhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. MDD Group (1) Meet the inclusion and exclusion criteria for clauses A, B, and C of Major Depressive Disorder (MDD) according to DSM-5; (2) Gender and age: No gender restriction, aged 12-18 years (stratified by male and female); (3) No severe heart, liver, or kidney diseases, no history of tumors, hematological disorders, rheumatism, malnutrition, or neurodegenerative diseases; (4) No use of immunomodulators or hormonal preparations within at least the past 6 months, and no use of antipyretic analgesics within the past 2 weeks; (5) Signed informed consent form. 2. Major Depressive Disorder with Suicidal Behavior (MDDSA) Group (1) Meet the inclusion and exclusion criteria for clauses A, B, and C of Major Depressive Disorder (MDD) according to DSM-5; (2) Meet the inclusion and exclusion criteria for clauses A, B, C, D, and E of Suicidal Behavior Disorder according to DSM-5; (3) Clinical manifestations meeting clause A criteria within the past 3 days; (4) Presence of suicidal ideation; (5) Gender and age: No gender restriction, aged 12-18 years (stratified by male and female); (6) No severe heart, liver, or kidney diseases, no history of tumors, hematological disorders, rheumatism, malnutrition, or neurodegenerative diseases; (7) No use of immunomodulators or hormonal preparations within at least the past 6 months, and no use of antipyretic analgesics within the past 2 weeks; (8) Signed informed consent form. 3. Healthy Control (HC) Group (1) Psychologically and physically healthy. (2) No history of self-harm, suicidal thoughts, or suicidal behaviors; (3) No history of psychiatric or psychological disorders; (4) Gender and age: No gender restriction, aged 12-18 years (stratified by male and female); (5) No severe heart, liver, or kidney diseases, no history of tumors, hematological disorders, rheumatism, malnutrition, or neurodegenerative diseases; (6) No use of immunomodulators or hormonal preparations within at least the past 6 months, no use of antipyretic analgesics within the past 2 weeks, and no history of psychoactive substance abuse.

Exclusion criteria

Exclusion criteria: 1. MDD Group (1) Presence of severe heart, liver, or kidney diseases, or history of tumors, hematological disorders, rheumatism, malnutrition, or neurodegenerative diseases; (2) Use of immunomodulators or hormonal preparations within the past 6 months, or use of antipyretic analgesics within the past 2 weeks; (3) Failure to sign the informed consent form. 2. Major Depressive Disorder with Suicidal Behavior (MDDSA) Group (1) Presence of severe heart, liver, or kidney diseases, or history of tumors, hematological disorders, rheumatism, malnutrition, or neurodegenerative diseases; (2) Use of immunomodulators or hormonal preparations within the past 6 months, or use of antipyretic analgesics within the past 2 weeks; (3) Failure to sign the informed consent form. 3. Healthy Control (HC) Group (1) Presence of severe heart, liver, or kidney diseases, or history of tumors, hematological disorders, rheumatism, malnutrition, or neurodegenerative diseases; (2) Use of immunomodulators or hormonal preparations within the past 6 months, use of antipyretic analgesics within the past 2 weeks, or history of psychoactive substance abuse; (3) Failure to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Speech emotion recognition model (based on continuous affective description model with AI learning);False positive rate and false negative rate of adolescent MDD screening;EEG rhythm characteristics (including power spectrum, symmetry of alpha band distribution, and nonlinear dynamical parameters);Event-related potential (ERP);Exosomal miRNA expression levels;Beck Suicide Ideation Scale (BSI-CV);Ottawa Self-Harm Inventory (OSI-CV);Patient Health Questionnaire-9 (PHQ-9);Generalized Anxiety Disorder-7 (GAD-7);Adolescent Stressful Life Events Checklist (ASLEC);Demographic characteristics (age, sex, body weight, height, education level, economic status, family members' self-harm or suicide history, parental marital status);

Secondary

MeasureTime frame
Clinical characteristics data (early trauma, diagnosis, treatment status, life events, depression, anxiety, self-harm and suicide behaviors, and suicide ideation);

Countries

China

Contacts

Public ContactTang Yiping

The Second People's Hospital Of Taizhou

zjtttyp@163.com+86 576 83979126

Outcome results

None listed

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