Intervention for the Treatment of Depression in Virtual Reality (FlowVR)
Not Applicable
- Conditions
- F32F32.1F32.2F32.8F32.9F33F33.1F33.2F33.8F33.9
- Registration Number
- DRKS00034078
- Lead Sponsor
- Asklepois Klinikum Harburg Zentrum für seelische Gesundheit Klinik für Psychiatrie, Psychotherapie und Psychosomatik
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Meeting the criteria for Major Depression, Dysthymia, or Recurrent Depressive Disorder according to DSM-5 verified (M.I.N.I.) with current episode, proficient in German language, providing written consent for study participation and the ability to give informed consent.
Exclusion Criteria
Patients with psychosis (including affective disorder with psychotic features), bipolar disorder, post-traumatic stress disorder, acute suicidality, and substance use disorder (currently not abstinent), as well as (partial) inpatient psychotherapy during the study.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is the change in mindfulness from T0 to T1 and from T0 to T2 (secondary), which is measured by using the Five Facet Mindfulness Questionnaire (FFMQ-D).
- Secondary Outcome Measures
Name Time Method