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Stress, Obesity, Liver fat, Insulin resistance in Depressio

Conditions
F32
F33
Depressive episode
Recurrent depressive disorder
Registration Number
DRKS00004324
Lead Sponsor
Zentralinstitut für Seelische Gesundheit
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
58
Inclusion Criteria

Patients: depressive episode (unipolar), severity: HDRS >= 18

Exclusion Criteria

Patients and controls:
not competent for consent, insufficient german language, diabetes, dyslipidemia, contraindication for MRI

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
This is a non-interventional trial. The above-mentioned dependent variables will be compared between healthy controls and depressed patients as well as between subgroups of depressed patients (e.g. high vs. low activity of the HPA system): functional imaging of the brain (MRI), breast and abdominal imaging (MRI), blood analysis for metabolic and genetic parameters, dexamethasone suppression test, cortisol in saliva and urine. This is a cross-sectional trial.
Secondary Outcome Measures
NameTimeMethod
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