F63.3 F63.8 F63.9
Conditions
Interventions
Group 1: Interventional = self-help intervention "Habit Replacement " for the treatment of BFRBs, which is sent as a PDF file by e-mail
Group 2: Wait-list control group = no additional treatment durin
receives access to self-help intervention after completion of the post-assessment
Sponsors
Universitätsklinikum Hamburg-Eppendorf, Klinik und Poliklinik für Psychiatrie und Psychotherapie, Arbeitsgruppe Klinische Neuropsychologie
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
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. 20 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: • lifetime schizophrenia • acute suicidal tendencies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total score of the Generic Body-Focused Repetitive Behavior Scale 45 (GBS-45) after the six-week intervention period (t0, t1) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Patient Health Questionnaire-9 (PHQ-9): Self-rating questionnaire measuring depressive symptoms during the past week (t0, t1). - Quality of life (WHO-QOL-BREF): Questionnaire that measures the quality of life in the last two weeks (t0, t1) - Questionnaire on patient satisfaction in modified version (ZUF-8): Self-report questionnaire that measures the global patient satisfaction at the end of treatment (t1) - Questionnaire for the subjective evaluation (t1) | — |
Countries
Germany
Contacts
Public ContactSteffen Moritz
Universitätsklinikum Hamburg-Eppendorf, Klinik und Poliklinik für Psychiatrie und Psychotherapie, Arbeitsgruppe Klinische Neuropsychologie
Outcome results
None listed