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europhenomenology of Deep Brain Stimulation for Depressio

Conditions
F33.2
F33.3
F33.8
F33.9
Recurrent depressive disorder, current episode severe without psychotic symptoms
Recurrent depressive disorder, current episode severe with psychotic symptoms
Other recurrent depressive disorders
Recurrent depressive disorder, unspecified
Registration Number
DRKS00016688
Lead Sponsor
niversitätsklinikum Freiburg
Brief Summary

A variety of qualitative insights into the effects of DBS were gained. For a summary, see the reporting sheet. The complete results of the interviews in the form of the bachelor’s thesis that was the result of the project can be made available upon request to the student that performed the project: Lucca-jaeckel@gmx.de

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
5
Inclusion Criteria

Participation one of the following clinical trials assessing the efficacy of deep brain stimulation for depression: FORESEE (ClinicalTrials.gov NCT01095263), FORESEE II (ClinicalTrials.gov NCT01778790), FORESEE III (ClinicalTrials.gov NCT03653858); Active treatment with DBS over the duration of at least 2 weeks

Exclusion Criteria

Acute psychotic or manic episode

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The study aims to obtain qualitative data, to assess the phenomenology of deep brain stimulation for depression after a treatment duration of at least 2 weeks.
Secondary Outcome Measures
NameTimeMethod
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