Online Prevention Program for Bereaved Siblings: A Randomised Controlled Trial
Not Applicable
- Conditions
- berreavement reactionsdepressionanxiety
- Registration Number
- DRKS00011514
- Lead Sponsor
- MSB Medical School Berlin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 86
Inclusion Criteria
1. Loss through death of a brother or a sister
2. Male and female
3. Adults (age 16-65)
4. Access to Internet
5. Germanspeaking
6. Signed letter of agreement
Exclusion Criteria
1. Suicidal tendency
2. High level of depression (BDI > 25)
3. Psychotic experiences
4. Increased use of alcohol, drugs or other substances
5. Persons attending a psychotherapeutical treatment
6. Selfinjuring behaviour
7. Borderline personality disorder
8. Bipolar disorder
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction of bereavement-specific symptoms (ICG, PTCI, IES), Depression (BDI-II) and Anxiety (PHQ-D) after the 6 weeks treatment.<br>
- Secondary Outcome Measures
Name Time Method Family cohesion (FB-K, EXIS), social support (BSSS), guilt (FIS) and working alliance (WAI) after the 6 weeks treatment and follow up (after 3, 6 and 12 months)<br>