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Changes and mechanisms of HPA axis and brain function in female patients with depression following childhood trauma

Changes and mechanisms of HPA axis and brain function in female patients with depression following childhood trauma

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000032078
Enrollment
Unknown
Registered
2020-04-19
Start date
2020-04-20
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

depression

Interventions

female depression with childhood trauma group:N/A
female depression without childhood trauma group:N/A
Healthy control group:N/A

Sponsors

Department of Psychosomatics and Psychiatry, Zhongda Hospital, School of Medicine, Southeast University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for the patient group: 1) female; 2) meet the diagnostic criteria of MDD in DSM-IV; 3) 17-item Hamilton depression scale (HAMD-17) score >= 17; 4) aged from 20 to 40 years; 5) history of electroconvulsive therapy; 6) right-handedness. Inclusion criteria for the healthy control group: 1) healthy women with age and education level matching the patient group were selected, and the HAMD-17 rating was < 8 (and the "depression mood" score was 0); 2) no history of serious heart, brain or kidney disease, no history of alcohol or drug abuse, no family history of mental illness; 3) no pacemaker or metal material in the body, and no t2-weighted MRI showed cerebral infarction or other vascular injuries in patients who were able to receive MRI examination; 4) right-handedness.

Exclusion criteria

Exclusion criteria: 1) severe suicidal tendencies; 2) had taken mood stabilizers, antipsychotics, or any antidepressant for treatment or drugs that may affect the activity of the HPA axis within 2 weeks prior to enrollment; 3) the previous history of other mental illness; 4) obvious abnormality in laboratory and auxiliary examination; 5) those who fail to cooperate with the examination or cannot complete the examination due to consciousness impairment or visual, hearing, speech and understanding impairment; 6) patients with a primary brain tumor, metastatic brain cancer, brain trauma, multiple sclerosis or severe physical diseases (including severe cardiopulmonary, liver and kidney dysfunction, shock, malignant tumor or blood disease, and autoimmune diseases); 7) t2-weighted MRI showed cerebral infarction or other vascular injuries; 8) patients with a pacemaker or metal material in the body cannot be examined by MRI.

Design outcomes

Primary

MeasureTime frame
MRI index;peripheral protein index;clinical scales;

Countries

China

Contacts

Public ContactYuan Yonggui

Zhongda Hospital, School of Medicine, Southeast University

yygylh2000@sina.com+86 025-83285124

Outcome results

None listed

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