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The development and application of diagnosis and treatment technology for adolescent emotional and behavioral disorders

The development and application of diagnosis and treatment technology for adolescent emotional and behavioral disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081375
Enrollment
Unknown
Registered
2024-02-29
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Adolescent emotional and behavioral disorders(Schizophrenia, Depression, Bipolar disorder)

Interventions

Schizophrenia group:Selecte one of the three antipsychotic drugs for treatment: risperidone, aripiprazole and olanzapine
Depression group:Selecte a single antidepressant of SSRI for treatment
BD group:Selecte one of the three mood stabilizers for treatment: risperidone, aripiprazole and olanzapine
healthy controls:none
Common rTMS treatment group:Common rTMS treatment
Image navigation accurate rTMS treatment group:Image navigation accurate rTMS treatment

Sponsors

He'nan Mental Hosptial
Lead Sponsor

Eligibility

Sex/Gender
All
Age
11 Years to 18 Years

Inclusion criteria

Inclusion criteria: SCZ inclusion criteria: 1. In the first acute stage of the disease, the duration of the disease is less than 3 years (the interval is not more than 6 months), which meets the DSM-5 diagnostic criteria of SCZ; 2. 11-18 years old, and at least one guardian shall monitor the patient within one year; 3. It is expected that there will be no problems such as relocation of residence, inconvenient transportation and difficulty in seeing a doctor during the whole study; 4. Obtain the informed consent from patients and guardians, and sign the informed consent form; 5. Selecte one of the three antipsychotic drugs for treatment: risperidone, aripiprazole and olanzapine. Depression inclusion criteria: 1. In the first acute stage of the disease, the duration of the disease is less than 3 years (the interval is not more than 6 months), which meets the DSM-5 diagnostic criteria of Depression; 2. 11-18 years old, and at least one guardian shall monitor the patient within one year; 3. It is expected that there will be no problems such as relocation of residence, inconvenient transportation and difficulty in seeing a doctor during the whole study; 4. Obtain the informed consent from patients and guardians, and sign the informed consent form; 5. Selecte a single antidepressant of SSRI for treatment. Bipolar Disorder inclusion criteria : 1. In the first acute stage of the disease, the duration of the disease is less than 3 years (the interval is not more than 6 months), which meets the DSM-5 diagnostic criteria of BD; 2. 11-18 years old, and at least one guardian shall monitor the patient within one year; 3. It is expected that there will be no problems such as relocation of residence, inconvenient transportation and difficulty in seeing a doctor during the whole study; 4. Obtain the informed consent from patients and guardians, and sign the informed consent form; 5. Selecte one of the three mood stabilizers for treatment: risperidone, aripiprazole and olanzapine. High-risk groups inclusion criteria: 1.Mild psychotic symptoms/short history of self-limited psychotic symptoms (self-resolution within 7 days)/positive family history of mental disorders and decreased social functioning; 2.No current physical illness; 3.11-18 years old, gender, education matched with patient groups; 4.Be able to cooperate with the completion of the project evaluation content; 5.Obtain the informed consent from patients and guardians, and sign the informed consent form; Healthy controls inclusion criteria: 1.Be in good health and have no mental illness meeting DSM-5 diagnostic criteria,screened for SCID; 2.No history of mental illness; 3.No current physical illness; 4.11-18 years old, gender, education matched with patient groups; 5. Be able to cooperate with the completion of the project evaluation content; 6.Obtain the informed consent from subjects and guardians, and sign the informed consent form; 7.No contraindication of magnetic resonance imaging (MRI).

Exclusion criteria

Exclusion criteria: SCZ/depression/BD patients exclusion criteria: 1.Serious somatic diseases or alcohol abuse; 2.Serious physical disability, unable to complete follow-up; 3.People suffering from other serious mental diseases, mental retardation, dementia and severe cognitive impairment; 4.Currently receiving or preparing to receive other clinical studies; High-risk groups exclusion criteria: 1.People with autism spectrum disorders; 2.Have a history of substance dependence; 3. Brain trauma, epilepsy or other organic brain diseases; 4. Laboratory examination shows liver and kidney function damage or other serious physical diseases and metabolic disorders; Healthy controls exclusion criteria: 1.Have a history of substance dependence; 2.Brain trauma, epilepsy or other organic brain diseases; 3.Have definite physical diseases such as hypertension and diabetes; 4.Laboratory examination shows liver and kidney function damage or other serious physical diseases and metabolic disorders; 5. Pregnant women or breast-feeding period.

Design outcomes

Primary

MeasureTime frame
Diagnostic evaluation;Adolescent behavioral and emotional assessment;Evaluation of psychiatric symptoms;Cognitive function assessment;Genetic Testing;Proteomic detection;Metabolomics detection;Neuroimaging detection;Neuroelectrophysiological tests;

Secondary

MeasureTime frame
Adverse reaction evaluation;Biochemical detection;Expressions, eye movements, language collection;

Countries

China

Contacts

Public ContactLi Wenqiang

He'nan Mental Hospita, the Second Affiliated Hospital of Xinxiang Medical University

lwq781603@163.com+86 185 3733 9679

Outcome results

None listed

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