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A Study on the Baseline Survey of Mental Disorders in Children and Adolescents and the Evaluation of the Effect of "Non pharmacological Comprehensive Psychological Intervention Model" in Tongzhou District

A Study on the Baseline Survey of Mental Disorders in Children and Adolescents and the Evaluation of the Effect of "Non pharmacological Comprehensive Psychological Intervention Model" in Tongzhou District

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082599
Enrollment
Unknown
Registered
2024-04-01
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

Attention Deficit Hyperactivity Disorder

Interventions

ADHD-intervention group:The combination of biofeedback therapy, repetitive transcranial magnetic stimulation therapy and general family guidance program
ADHD-control group:The general family guidance program
Anxiety disorder-intervention group:Interview psychotherapy combined with general family guidance program
Anxiety disorder-control group:The general family guidance program

Sponsors

Tongzhou Maternal& Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 16 Years

Inclusion criteria

Inclusion criteria: (1) the abnormal children were investigated in the study design (1), and the children and adolescents aged 6 to 16 who took the initiative to see a doctor in our hospital because of mental health problems and met the diagnostic criteria of ICD-11 and/ or DSM-5. (2) the informed consent form signed by the patient and the guardian. (3) the patient and the guardian can cooperate to complete the scale evaluation.

Exclusion criteria

Exclusion criteria: (1) previously diagnosed mental disorders such as mental retardation, schizophrenia, schizophrenic affective disorder and other diseases. (2) patients who have been intervened by psychotropic drugs in the past year. (3) patients with contraindications to the use of intervention instruments. (4) patients with other conditions that the researchers believe are not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
SNAP-IV;Hamilton Anxiety Scale;

Secondary

MeasureTime frame
Conners;The Strengths and Difficulties Questionnaire;

Countries

China

Contacts

Public ContactYang Li

Tongzhou Maternal& Child Health Hospital

bjtzfy@126.com+86 136 8106 4933

Outcome results

None listed

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