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A cross-sectional study on adolescent mental health risk early warning and screening in Nanjing

A cross-sectional study on adolescent mental health risk early warning and screening in Nanjing

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400085669
Enrollment
Unknown
Registered
2024-06-14
Start date
2024-06-17
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

depression

Interventions

A (adolescent male aged 12-15):None
B (adolescent male aged 16-18):None
C(Female women aged 12-15):None
D (adolescent women aged 16-18):None

Sponsors

Jiangsu Provincial Center for Disease Control and Prevention
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: (1) Samples must be stored at room temperature, centrifuged within 4 hours after collection, transferred to-60? within 10 hours, and then stored until testing; (2) The subject age is 12-18 years old, and the gender is not limited; (3) The subject and his legal guardian can communicate well with the investigator, understand and comply with the requirements of the study, participate voluntarily, and be willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) The sample showed blood coagulation or hemolysis phenomenon; (2) Incorrect collection or storage of samples; (3) The subject is known to have other psychiatric disorders; (4) Patients with neurological diseases, brain trauma, cardiovascular and cerebrovascular diseases, severe liver and kidney function abnormalities, diabetes mellitus and other major physical diseases; (5) Receiving oral treatment or injection of hormone drug therapy in the latest week; (6) Patients with a history of surgery within the recent 3 months and hospitalization for more than 1 week; (7) Samples considered by the investigator to have other inappropriate factors to participate in this trial.

Design outcomes

Primary

MeasureTime frame
The coincidence rate of "inferred positive" and "positive" of ten diagnostic biomarkers for depression;Reference interval of serum concentration of various metabolites (liquid chromatography-tandem mass spectrometry) in Nanjing adolescents;Concentration of various metabolites and results of omics analysis in adolescent serum samples from Nanjing.;

Countries

China

Contacts

Public ContactSun Xiang

Jiangsu Provincial Center for Disease Control and Prevention

sunstone1@163.com+86 153 6517 3126

Outcome results

None listed

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