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Neuroimaging mechanism of oxytocin improving social cognition in schizophrenia through regulating the prefrontal-amygdala neural network

Neuroimaging mechanism of oxytocin improving social cognition in schizophrenia through regulating the prefrontal-amygdala neural network

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058730
Enrollment
Unknown
Registered
2022-04-15
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

schizophrenia

Interventions

Schizophrenia oxytocin intervention group:Oxytocin intervention
Schizophrenia placebo intervention group:normal saline
Clinical high-risk population oxytocin intervention group:Oxytocin intervention
Clinical high-risk group placebo intervention group:normal saline
Healthy control oxytocin intervention group :Oxytocin intervention
Healthy control placebo intervention group :normal saline

Sponsors

First Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patient group: 1. Comply with DSM-5 clinical diagnostic criteria for schizophrenia; 2. Age 15-40 years; 3. Gender is not limited; 4. Han nationality; 5. Right handed; 6. At least two doctors at or above the level of attending should make diagnosis according to SCID-5 and meet DSM-5 diagnostic criteria for schizophrenia; 7. The patient and his/her family/guardian agreed to participate in the study and signed the informed consent. High risk group: 1. It is confirmed that it meets the diagnostic criteria of prodromal syndrome and has not received drug treatment through stereotyped interview of psychiatric risk syndrome; 2. The rest are the same as the patient group; Healthy control group: 1. No history of mental illness or family history of mental illness; 2. Age 15-40 years; 3. Gender is not limited; 4. Han nationality; 5. Right handed.

Exclusion criteria

Exclusion criteria: Patient group: 1. DSM-5 diagnosed as schizophrenic affective disorder, attention deficit and hyperactivity disorder, substance abuse induced mental disorder, mood disorder, mental retardation, generalized developmental disorder, delirium, dementia, memory disorder or other cognitive disorders; 2. Women are pregnant or lactating or have a pregnancy plan in the next six months; Suffering from severe unstable somatic diseases; 3. Color blindness, glaucoma or other eye diseases; 4. Persons with epilepsy history; 5. There are serious suicide attempts or serious excitement; 6. Those who cannot accurately understand the contents of various mental health assessment scales or complete computer operation, or have no guardians. High risk group: 1. DSM-5 patients diagnosed as schizophrenia, the rest are the same as the patient group. Healthy control group: 1. Have material dependence, or take drugs that may affect mental and cognitive functions, or have received antipsychotic treatment; 2. Suffering from nervous system diseases such as brain organic diseases, or other serious physical diseases; 3. Women are pregnant or lactating or have a pregnancy plan in the next six months; 4. Perceptual development disorder, color blindness, or other eye diseases that affect vision.

Design outcomes

Primary

MeasureTime frame
Yoni task;Chinese version of the Movie for the Assessment of Social Cognition(MASC-C);VR task;

Secondary

MeasureTime frame
Positive and negative symptom scale(PANSS);Clinical global impressions scale(CGI);Electroencephalogram(EEG);Multimodal NMR data;MATRICS Consensus Cognitive Battery(MCCB);Social support rating scale(SSS);Revised adult attachment scale(AAS);

Countries

China

Contacts

Public ContactWang xiao

Shanxi Medical University

515787163@qq.com+86 15120079832

Outcome results

None listed

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