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fOCUS: intensief doorpakken met jongeren met OCD


- candidate number24073
- NTR NumberNTR5771
- ISRCTNISRCTN no longer applicable
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR7-mrt-2016
- Secondary IDsNL49574.072.14 
- Public TitlefOCUS: intensief doorpakken met jongeren met OCD
- Scientific TitleShort intensive 8 day CBT for children (age 15+) with OCD, who are nonremitter to regular CBT.
- ACRONYM
- hypothesisPatients will improve significantly on OCD symptoms and general functioning.
- Healt Condition(s) or Problem(s) studiedObsessive-compulsive disorder (OCD)
- Inclusion criteriaAge 15-19
A primary diagnosis of OCD (assessed with MINI)
Nonremitter to a adequate dose of regular CBT (with ERP).
CY-BOCS score of 16 (or 10 in case of pure obsessions)
- Exclusion criteriaSevere unstable mental disorder like depressive disorder, risk of suicide (assessed with MINI), severe autism spectrum disorders, severe family malfunctioning, severe cognitive malfunction, mental retardation; Patient (and family) are not able to focus on intensive treatment for 2 weeks because of social problems. Inability to read, write or speak in the Dutch language; Patient is not able to taper off drugs or alcohol use.
- mec approval receivedyes
- multicenter trialno
- randomisedyes
- masking/blindingNone
- controlNot applicable
- groupParallel
- TypeSingle arm
- Studytypeintervention
- planned startdate 1-mei-2016
- planned closingdate1-mei-2019
- Target number of participants10
- InterventionsIn the present study, intensive CBT treatment will be delivered in 8 days (in two weeks). CBT will take place in different locations, at home, etc. After the intensive phase, patients will receive 4 boostersessions of 90 minutes during the following 4 weeks and an evaluation session. There is a baseline phase, which is the control for the active phase.
- Primary outcomeOCD symptoms
- Secondary outcomeGeneral functioning
Quality of life
- TimepointsThe study consists of 4 phases, the baseline phase, the intervention phase, the post intervention phase and the follow-up. During the total study duration of 19 weeks, patiens have weekly assessments of their main symptoms. Before and after every phase the secondary outcome measures are assessed. (4 assessments in total.).
- Trial web site
- statusplanned
- CONTACT FOR PUBLIC QUERIES M Kampman
- CONTACT for SCIENTIFIC QUERIES M Kampman
- Sponsor/Initiator Pro Persona
- Funding
(Source(s) of Monetary or Material Support)
None
- Publications
- Brief summaryChildren (age 15-19) with OCD, who are noremitters on regular CBT, will receive an intensive 8-day CBT, followed by 4 weekly boostersessions, The study uses a multiple baseline design. primary outcomes are assessed in 4 phases. The patients are recruited in the Netherlands.
- Main changes (audit trail)
- RECORD7-mrt-2016 - 25-mei-2016


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