Effectiveness of Imagery Rescripting for depression - a one-armed pilot study
Not Applicable
- Conditions
- F32Depressive episode
- Registration Number
- DRKS00034273
- Lead Sponsor
- niversität zu Lübeck
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Primary diagnosis of depression, with at least moderate severity (> 16 points in the Hamilton Rating Scale for Depression (HRSD-24) and aversive childhood experiences (recorded with the Childhood Trauma Questionnaire (CTQ): Sum score on at least one of the CTQ subscales for sexual, physical, emotional abuse or emotional neglect above the cut-off for moderate abuse), 18-65 years, informed consent, sufficient knowledge of German (also in writing)
Exclusion Criteria
Post-traumatic stress disorder, psychotic/bipolar disorder, IQ < 85, acute suicidal tendencies/substance dependence, use of benzodiazepines/opiates, severe physical illness that impairs learning ability, previous Imagery Rescripting treatment (> 2 sessions)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is the severity of depressive symptoms at follow-up 1 (six month after start of treatment) assessed with Hamilton Rating Scale for Depression (HRSD-24)
- Secondary Outcome Measures
Name Time Method