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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06388486
Other study ID # UMCGoettingen9/9/16
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date January 1, 2024

Study information

Verified date April 2024
Source University Medical Center Goettingen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to measure the levels of cytokine-induced transcription factor activation in a cohort of depressed inpatients undergoing psychotherapy. The study aims to answer the following main questions: - Do psychological traits (i.e.: social inhibition, negative affectivity, ...) affect the activation of immunomodulatory transcription factors (STAT3, NFkB) in depressed patients? - Are subjects with these psychological traits affected differently by psychotherapeutic intervention? Study subjects are assessed for their psychological and behavioral traits and receive psychotherapeutic care over several weeks during hospital treatment. Peripheral blood mononuclear cells are isolated from the study subjects, and activation of transcription factors is measured by flow cytometry.


Description:

Study subjects are assessed for their psychological and behavioral traits and receive psychotherapeutic care over several weeks during hospital treatment. Peripheral blood mononuclear cells are isolated from the study subjects, and activation of transcription factors is measured by flow cytometry.


Recruitment information / eligibility

Status Completed
Enrollment 63
Est. completion date January 1, 2024
Est. primary completion date March 9, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Diagnosis of current depression Exclusion Criteria: - inadequate knowledge of the German language - unable to give informed consent - severe psychiatric comorbidities, such as drug abuse and psychotic diseases - deemed critically unstable by their treating physician

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Psychotherapy
Subject receive psychotherapy during hospital treatment.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Medical Center Goettingen

Outcome

Type Measure Description Time frame Safety issue
Primary Change in depression Hospital Depression and Anxiety Scale (HADS). The HADS instrument is a 14-item scale, with seven items relating to anxiety and seven relating to depression item. Each item on qestionnaire is scored from 0-3 resulting in a score between 0 and 21 for either anxiety or depression with higher scores meaning a worse outcome. 6 weeks
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