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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04306835
Other study ID # 143201836242
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 22, 2018
Est. completion date March 2020

Study information

Verified date March 2019
Source Universitair Ziekenhuis Brussel
Contact Jasper Molenberghs
Phone 0494182014
Email jasper.molenberghs@vub.be
Is FDA regulated No
Health authority
Study type Interventional

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date March 2020
Est. primary completion date March 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- All patients, male and female, with an OSAS diagnosed by full polysomnography and insomnia diagnosed by questionnaires.

- Age between 18 and 75 years

- Dutch as native language

Exclusion Criteria:

- Patients younger than 18 years and older than 75 years

- Patients with a burn-out

- Patients with restless legs

- Pregnant woman

- Patients who work as shift workers

- Patients with severe psychiatric disorder

- Patients who take sleep medication, unless it can be reduced and stopped during cognitive behavior therapy

- Patients with daily alcohol abuse (men > 3 drinks on any day or 14 per week, women > 2 drinks on any day or 7 per week)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive behavioural therapy for insomnia
a technique for treating insomnia without medications

Locations

Country Name City State
Belgium UZ Brussel Jette Brussels

Sponsors (1)

Lead Sponsor Collaborator
Universitair Ziekenhuis Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of drop-outs in patients participating in the study. Patiƫnt who don't use there CPAP anymore. 12 weeks
Primary CPAP habituation in patients participating in the study. The speed of CPAP habituation is determined by reading the CPAP device. 12 weeks
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