Transdiagnotic internet-based and mobile-supported intervention for the treatment of depressio
Not Applicable
- Conditions
- F32F41.9F41.1F40Depressive episodeAnxiety disorder, unspecifiedGeneralized anxiety disorderPhobic anxiety disorders
- Registration Number
- DRKS00011690
- Lead Sponsor
- Friedrich-Alexander Universität Erlangen-Nürnberg, Lehrstuhl für Klinische Psychologie und Psychotherapie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Minimum age 18; Signed consent form; Clinical diagnosis of depression determined by diagnostic interview
Exclusion Criteria
Acute suicidal tendency determined by initial diagnostic interview; unwilling to sign the consent form; psychotherapeutical treatment in the last 6 months or on waiting list for psychotherapy; self-report on present psychosis or dissociative symptoms; bipolar disorder in the past or present
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Symptom severity of depression at time of post-measurement determined by: <br>• Diagnostic interview (QIDS-C, Rush, Trivedi, Ibrahim, Carmody, Arnow, et al., 2003), time of measurement at Baseline (t1), Post (t2) and 6 months follow-up (t3) <br>• Self-report (CES-D, Radloff, 1977; PHQ-9, Kroenke, Spitzer, Williams, 2001), CES-D on a weekly Basis (week 1 - 7), at t0, t1, t2, t3; PHQ at t1, t2, t3<br>t0 = Screening, before study inclusion<br>t1 = Baseline<br>t2 = Posttreatment (after completion of module 7 or after 8 weeks)<br>t3 = 6-month follow-up<br>
- Secondary Outcome Measures
Name Time Method