obsessive-compulsive disorder OCD
Conditions
Interventions
One group will receive exposure with response prevention as usual, the other
group will receive exposure with response prevention with smartphone
application NiceDay.
Sponsors
Parnassia (Den Haag)
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameter is a difference in treatment outcome as measured with the Yale Brown Obsessive-Compulsive Scale (YBOCS) and the World Health Organization Quality of Life (WHOQOL-bref) | — |
Secondary
| Measure | Time frame |
|---|---|
| The 16-item self-report Quick Inventory of Depressive Symptomatology (QIDS) The Positive and Negative Affect Schedule (PANAS) The NEO Five Factor Inventory (NEO-FFI) The State-Trait Anxiety Inventory (STAI) General Self-Efficacy Scale (GSES) Treatment Credibility Questionnaire (TCQ) Technology Acceptance Model (TAM) Experience sampling data Log data NiceDay The Prodromal Questionnaire (PQ-16) The Trauma Screening Questionnaire (TSQ) Screener for Substance Abuse | — |
Countries
Netherlands
Outcome results
None listed