Efficacy and feasibility of software for the treatment of obsessive compulsive disorder: a pilot study
Not Applicable
- Conditions
- Obsessive compulsive disorder
- Registration Number
- JPRN-UMIN000048120
- Lead Sponsor
- Kyoto University
- Brief Summary
Three patients participated in the study. The OCD symptoms and depression improved in all the patients(Y-BOCS 21 to 16, 21 to 6, 18 to 13; OCI 46 to 18, 23 to 14, 40 to 27; PHQ-9 4 to 1, 12 to 3, 16 to 10). The symptoms of anxiety did not change or worsen (OASIS 4 to 4, 2 to 3, 7 to 7). The sessions completed were 10 (25%), 19 (47.5%), 13 (32.5%).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 3
Inclusion Criteria
Not provided
Exclusion Criteria
High risk of suicide, self-harm, admission. Those who cannnot answer the questionnaire du to the lack of ability. Those who don't have computer or smartphone. Those who have received CBT or those who will receive CBT during this trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method