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RecruitingNCT06580860PMNPUpdated Mar 13, 2026

Psychiatric Multi-omics and Neuroimaging Project

An observational study in Mental Disorders and Healthy Control, sponsored by mingjun Zhong. Recruiting at 1 site in China. Open to participants aged 13 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-13.

Sponsored by mingjun Zhong · Observational

From the registry’s dates

  • Started Jan 2016; still recruiting 10 years 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,899
Ages
13 Years to 35 Years
Sex
All
01

Study summary

This study focuses on the structure and function of the brain and gene expression in peripheral blood of patients with schizophrenia, to explore the interaction and influence between the three. Patients with mental disorders who have been recruited will take their medication regularly for 1 year and participate in baseline and follow-up assessments.

Read the detailed description

The study seeks to identify possible biological markers of schizophrenia and the effects of gene-environment interactions on brain structural and functional networks. So we can help doctors and scientific researchers better understand the neuropathological basis of schizophrenia.

02

Conditions studied

  • Mental Disorders
  • Healthy Control

Keywords

  • schizophrenia
  • major depressive disorder
  • autism spectrum disorder
  • bipolar disorder
  • magnetic resonance imaging
  • multi-omics
03

In context

Mental Disorders

2,107 studies on the registry are indexed under Mental Disorders; 416 are open to participants now.

This study's planned enrollment of 1,899 is above the median of 200 across 480 observational studies indexed under Mental Disorders.

Browse Mental Disorders studies →

Lead sponsor

This is the only study on the registry with mingjun Zhong as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Patients from inpatient and outpatient the second Xiangya Hosptial of Central South University, Healthy controls from community, school and street recruitment

Inclusion criteria

  • Age: 13-35 years old(Patients with healthy siblings can be extended to 14-35 years of age)
  • Course of disease: \<24 months
  • Priority is given to patients who have never taken medicine or duration of drug use \< 2 weeks
  • No nuclear magnetic contraindications.

Exclusion criteria

Exclusion Criteria:

  • Family history of psychotic disorders, history of psychoactive substances abuse, alcohol dependence, or nicotine dependence
  • Have a major physical disease or infectious disease
  • History of coma and serious neurological disease 4.MRI contraindications.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,899 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • PMNP-Healthy Norms

    Healthy Norms

    Drug: Antipsychotic drugs, antidepressants, mood stabilizers, and sleep aids

  • PMNP-Subclinical high-risk

    Subclinical high-risk

    Drug: Antipsychotic drugs, antidepressants, mood stabilizers, and sleep aids

  • PMNP-Schizophrenia and Psychosis

    Schizophrenia and Psychosis patient

    Drug: Antipsychotic drugs, antidepressants, mood stabilizers, and sleep aids

  • PMNP-MDD

    major depressive disorder patient

    Drug: Antipsychotic drugs, antidepressants, mood stabilizers, and sleep aids

  • PMNP-ASD

    autism spectrum disorder patient

    Drug: Antipsychotic drugs, antidepressants, mood stabilizers, and sleep aids

  • PMNP-BD

    bipolar disorder patient

    Drug: Antipsychotic drugs, antidepressants, mood stabilizers, and sleep aids

Interventions

  • DrugAntipsychotic drugs, antidepressants, mood stabilizers, and sleep aids

    Patients with mental disorders should take the appropriate medicine as prescribed by the doctor,and the health norms are not required to take medicine.This study will not interfere with the medication regimen of doctors.

06

What researchers measure

Primary outcomes

  1. cortical morphology

    Data were obtained using magnetic resonance scans

    Time frame: 40 minutes

  2. target gene charaacteristics

    10ml peripheral blood was extracted for gene analysis

    Time frame: 1 day

  3. scale scores

    The score of each dimension and the total score were calculated according to the scale.The scale includes three dimensions: negative symptom, positive symptom and general psychopathology, and the score range of each dimension is different. The total score ranges from 30 to 210, with higher scores indicating worse results.

    Time frame: 90 minutes.

07

Study locations

1 of 1 sites recruiting
  • The Second Xiangya hospital of central south univerity
    Changsha, Hunan 410000, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06580860
Lead sponsor
mingjun Zhong
Responsible party
mingjun Zhong (Principal Investigator, Second Xiangya Hospital of Central South University) — Sponsor-investigator
First posted
Aug 30, 2024
Start date
Jan 2016
Primary completion
Jan 2027 (estimated)
Completion
Jan 2027 (estimated)
Last update
Mar 13, 2026

Study contacts

Yunzhi Pan
Contact
panyunzhi@csu.edu.cn
15074818197

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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