F63.3 F63.8 F63.9
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: · consent to participate in study (informed consent) · internet access · sufficient command of the German language · willingness to participate in two anonymous online surveys, each of which lasts approx. 25-30 minutes · willingness to participate in a 6-week training program · willingness to use the program on one's own responsibility · willingness to provide an e-mail address
Exclusion criteria
Exclusion criteria: · Diagnosis of schizophrenic or bipolar disorder · Acute suicidal tendencies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total score of the Generic Body-Focused Repetitive Behavior Scale (GBS-45) | — |
Secondary
| Measure | Time frame |
|---|---|
| · Patient Health Questionnaire-9 (PHQ-9): Self-rating questionnaire measuring depressive symptoms during the past week (at baseline- and post-assessment) · Quality of life (WHO-QOL-BREF): Global score of the self-assessment questionnaire; measures the quality of life in the last two weeks (at baseline- and post-assessment) · Rhode Island Change Assessment Scale (URICA): Self-rating questionnaire assessing the stages of change (at baseline- and post-assessment) · Patient satisfaction (ZUF-8): Self-assessment questionnaire measuring patient satisfaction regarding the treatment received (post-assessment) · Positive and Negative Effects of Psychotherapy Scale (PANEPS-I): Self-report questionnaire to measure positive effects and unwanted events (e.g., possible side effects) during the intervention (post-assessment) · Questionnaire for the subjective evaluation of the self-help measures and the website (post-assessment) | — |
Countries
Germany
Contacts
oUniversitätsklinikum Hamburg-Eppendorf, Klinik und Poliklinik für Psychiatrie und Psychotherapie, Arbeitsgruppe Klinische Neuropsychologie