Evaluation of an app for self-directed processing of therapeutic content for patients with unipolar depressio
Not Applicable
- Conditions
- F32.0F32.1F32.2F33.0F33.1F33.2Mild depressive episodeModerate depressive episodeSevere depressive episode without psychotic symptomsRecurrent depressive disorder, current episode mild
- Registration Number
- DRKS00033782
- Lead Sponsor
- niversitätsklinikum Bonn
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 62
Inclusion Criteria
Previous diagnosis of unipolar depression by experts or current diagnosis as part of the study assessment
Current minimum sum score of 9 on the GRID-HAMD17 rating
Ongoing medication, psychotherapy or other S3 guideline-compliant treatment for depression
Sufficient understanding of the German language
Exclusion Criteria
Signs of increased risk of suicidal tendencies (GRID-HAMD Item 3 score greater than 2)
Psychotic symptoms
Bipolar disorder/manic symptoms
Disorders belonging to the schizophrenia spectrum
Substance dependence
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in depression symptoms by means of PHQ-9 following a four-week intervention.
- Secondary Outcome Measures
Name Time Method sability measured by the System Usability Scale (SUS)<br>Satisfaction with the digital intervention (CSQ-I)<br>Change in Generalizied Anxiety Disorder Scale (GAD-7)<br>Change in behavioral activation (BADS)<br>Change in subjective perception of stress (PSS)<br>Change in psychological resilience (RS)<br>Change in self-esteem (RSES)<br>Change in bias due to negative interpretation (AST-D-II)<br>Change in subjective quality of life (WHOQoL)<br>Change in depressive symptoms according to ICD-11 criteria (IDQ)<br>Change in anxiety symptoms (IAQ) <br>Subjective assessment of efficacy of the respective modules<br>Survey of adverse events <br>Knowledge transfer of the therapy content