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Mechanisms of anhedonic neurocircuitry in depression: a multimodal imaging-genomics integrated analysis

Mechanisms of anhedonic neurocircuitry in depression: a multimodal imaging-genomics integrated analysis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120156
Enrollment
Unknown
Registered
2026-03-10
Start date
2025-12-24
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Depression

Interventions

Normal control group:Non
Depression without anhedonia group:None
Depression with anhedonia group:None

Sponsors

Hangzhou Seventh People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patient group: 1.Age: 18-45 years old (inclusive); 2.Ethnicity: Han Chinese; 3.Handedness: Right-handed; 4.Episode: First-episode patients; 5.Education & functioning: Primary school graduate or above, with premorbidly normal social functioning; 6.Diagnosis: Meeting diagnostic criteria for major depressive disorder according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5); 7.Medication history: No prior use of any antipsychotics, antidepressants, benzodiazepines, or other central nervous system (CNS)-acting medications or antidepressant monotherapy for 5. Normal control group: 1.Age: 18-45 years old (inclusive); 2.Ethnicity: Han Chinese; 3.Handedness: Right-handed; 4.Education: Primary school graduate or above; 5.Functioning: Intact social functioning; 6.Consent: Voluntary participation and provision of informed consent.

Exclusion criteria

Exclusion criteria: Patient group: 1.History of organic brain disease, neurological disorders, or severe endocrine/metabolic diseases; 2.History of traumatic brain injury with associated coma; 3.Prior diagnosis of other psychiatric disorders according to DSM-5 criteria; 4.Non-cooperative or unable to effectively complete study examinations; 5.Presence of fixed metal dental prostheses, cardiac pacemakers, or other metal implants; 6.Pregnant or lactating women. Normal control group: 1.History of any psychiatric disorder diagnosed by DSM-5 criteria; 2.History of traumatic brain injury with associated coma; 3.Positive family history of mental illness (first- and second-degree relatives within three generations); 4.History of psychotropic medication use (e.g., antipsychotics, antidepressants); 5.Presence of fixed metal dental prostheses, cardiac pacemakers, or other metal implants; 6.Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Anhedonia scores;

Secondary

MeasureTime frame
Peripheral metabolite indicators;General and clinical information;Anxiety scores;Depressive symptom scores;Brain functional connectivity level;

Countries

China

Contacts

Public ContactSugai Liang

Hangzhou Seventh People's Hospital

sgl011@163.com+86 15928421891

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026