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PERSONALIZED EXPOSURE AND ESM FEEDBACK VERSUS EXPOSURE AS USUAL FOR OCD

Recruiting
Conditions
obsessive-compulsive disorder
OCD
10002861
Registration Number
NL-OMON55600
Lead Sponsor
Parnassia (Den Haag)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
160
Inclusion Criteria

In order to be eligible to participate in this study, a subject must meet all
of the following criteria: A OCD diagnosis according to DSM 5 criteria, with
further psychometric profiling using non-DSM based (multidimensional) rating
scales.

Exclusion Criteria

Severe comorbidity in the psychiatric field (psychosis,
addiction/intoxication), insufficient fluency in the Dutch language, medication
use that has not been stable for 3 months.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main study parameter is a difference in treatment outcome as measured with<br /><br>the Yale Brown Obsessive-Compulsive Scale (YBOCS) and the World Health<br /><br>Organization Quality of Life (WHOQOL-bref)</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>The 16-item self-report Quick Inventory of Depressive Symptomatology (QIDS)<br /><br>The Positive and Negative Affect Schedule (PANAS)<br /><br>The NEO Five Factor Inventory (NEO-FFI)<br /><br>The State-Trait Anxiety Inventory (STAI)<br /><br>General Self-Efficacy Scale (GSES)<br /><br>Treatment Credibility Questionnaire (TCQ)<br /><br>Technology Acceptance Model (TAM)<br /><br>Experience sampling data<br /><br>Log data NiceDay<br /><br>The Prodromal Questionnaire (PQ-16)<br /><br>The Trauma Screening Questionnaire (TSQ)<br /><br>Screener for Substance Abuse</p><br>
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