NL-OMON49752CompletedNot Applicable
Confidence in context in obsessive-compulsive disorder. - Confidence in context
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Academisch Medisch Centrum
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 to 99 (—)
Inclusion Criteria
- •Inclusion process: Potential participants are informed about the study and will
- •receive an information letter. After this, they are contacted by telephone. If
- •interested to participate, screening for inclusion and exclusion criteria is
- •performed. In order to be eligible to participate in this study, a subject must
- •meet all of the following criteria:
- •OCD subject:
- •- DSM-5 diagnosis of OCD
- •- No other psychiatric disorder
- •- Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) score cut-off of 12
- •- 18-65 years of age
- •- Willingness and ability to give written informed consent and willingness and
- •ability to understand, to participate and to comply with the study requirements
- •HC subject:
- •- No current psychiatric diagnosis or history of OCD.
- •- 18-65 years of age
- •- Willingness and ability to give written informed consent and willingness and
- •ability to understand, to participate and to comply with the study requirement
Exclusion Criteria
- •All groups:
- •- Current major depressive disorder, bipolar disorder, psychotic disorder,
- •alcohol or substance dependence, or any cognitive disorder as assessed with the
- •MINI neurological disorders section
- •- IQ below 80
- •- Insufficient command of the Dutch language
- •- recent (<2 weeks) use of psychotropic medication other than naltrexone
- •(smoking and nicotine dependence is allowed in all groups).
- •- Endocrinological disorders or regular use of corticosteroids
- •- Current treatment with SSRIs, tricyclic antidepressant or antipsychotic
- •- Use of other psychotropic medication or recent use of recreational drugs over
- •a period of 72 hours prior to each test session, and use of alcohol within the
- •last 24 hours before each measurement.
Investigators
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