F63.3 F63.8 F63.9 F98.8
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • consent to participate in study (informed consent) • internet access • sufficient command of the English language • willingness to participate in two anonymous online surveys • 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 (GBS). | — |
Secondary
| Measure | Time frame |
|---|---|
| • Repetitive Body Focused Behavior Scale (RBFBS), self-report scale, adapted for adults • Patient Health Questionnaire-9 (PHQ-9): Self-rating questionnaire measuring depressive symptoms during the past week (at baseline- and post-assessment). • Self-devised questionnaire asking for the differential efficacy of the three techniques conveyed (post only, only administered in those using the techniques). • Questionnaire for the subjective evaluation of the self-help measures • Quality of life (WHO-QOL-BREF): Global score of the self-assessment questionnaire; this measures the quality of life in the last two weeks (at baseline- and post-assessment). • Questionnaire on patient satisfaction in modified version (ZUF-8): Self-report questionnaire that measures the global patient satisfaction at the end of treatment (at post-assessment). | — |
Countries
Austria, Germany, Switzerland
Contacts
Universitätsklinikum Hamburg-Eppendorf, Klinik und Poliklinik für Psychiatrie und Psychotherapie, Arbeitsgruppe Klinische Neuropsychologie