Internet-delivered Attention Training for Obsessive-Compulsive Disorder
- Conditions
- Obsessive-Compulsive Disorder
- Registration Number
- NCT02018848
- Lead Sponsor
- Humboldt-Universität zu Berlin
- Brief Summary
The goal of this study is to investigate an attention training program for participants with Obsessive-Compulsive Disorder. The attention training consists of a modified dot probe task with picture stimuli related to washing and checking paired with neutral pictures.
Participants are randomly assigned to an experimental and a placebo-control group. After a minimum of 4 weeks of attention training we expect to find differences between participants of the experimental and the control group in terms of attention bias, OCD symptoms, anxiety and depression.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 108
- diagnosis of primary OCD according to OCI-R self report (cut-off >=18)
- suicidal
- substance abuse or addiction
- psychotic symptoms
- visual impairment if not compensated with optical aid
Current treatment is not an exclusion criterion, but data on treatment status (current psycho- or pharmacotherapy for OCD) will enter our statistical analyses.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Yale-Brown Obsessive-Compulsive Scale Self-Report Scale (Y-BOCS-SRS) T1 pre-treatment, estimated: between day 1 and day 7 after enrolment (no time limit set) The Y-BOCS-SRS measures severity of OCD symptoms.
Yale-Brown Obsessive-Compulsive Scale Self-Report Scale (Y-BOCS-SRS) T2 post-treatment, between day 1 and 6 after T2 Bias Assessment (time limit set) The Y-BOCS-SRS measures severity of OCD symptoms.
Yale-Brown Obsessive-Compulsive Scale Self-Report Scale (Y-BOCS-SRS) T3 follow-up, between day 27 and 50 after T2 questionnaires (time limit set) The Y-BOCS-SRS measures severity of OCD symptoms.
- Secondary Outcome Measures
Name Time Method Obsessive-Compulsive Inventory-Revised (OCI-R) T1 pre-treatment, estimated: between day 1 and day 7 after enrolment (no time limit set) The OCI-R measures severity of OCD symptoms.
Obsessive-Compulsive Inventory-Revised (OCI-R) T2 post-treatment, between day 1 and 6 after T2 Bias Assessment (time limit set) The OCI-R measures severity of OCD symptoms.
Obsessive-Compulsive Inventory-Revised (OCI-R) T3 follow-up, between day 27 and 50 after T2 questionnaires (time limit set) The OCI-R measures severity of OCD symptoms.
Trial Locations
- Locations (1)
Humboldt-Universität zu Berlin
🇩🇪Berlin, Germany
Humboldt-Universität zu Berlin🇩🇪Berlin, Germany