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Clinical Trial Summary

Patients follow the fully standard sleep test according to the normal procedure. This means that they undergo a polysomnography and fill in a questionnaire. If according to the questionnaire, there is insomnia, the patient also receives an intake interview to check whether this is indeed the case. If the patient has both disorders and meets the inclusion and exclusion criteria, they will be asked to sign the informed consent. If the patient agrees, the CPAP-therapy will be started as usual, simultaneously with CGT-i. The latter will last 7 weeks and will cover the following points: psycho-education, sleep restriction and sleep hygiene, cognition, relaxation and relapse prevention. Because of the design of this study (starting CGT-I as soon as possible after the diagnosis of OSAS) and the groups already planned for CBT-I, it is not possible for all participants to participate in group cognitive behavioral therapy, therefore individual sessions were provided for these participants. The patient comes for monitoring at set times.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04306835
Study type Interventional
Source Universitair Ziekenhuis Brussel
Contact Jasper Molenberghs
Phone 0494182014
Email jasper.molenberghs@vub.be
Status Recruiting
Phase N/A
Start date October 22, 2018
Completion date March 2020

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