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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01704352
Other study ID # 2012/1033
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2013
Est. completion date August 2018

Study information

Verified date November 2018
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with bipolar disorder suffer from sleep disturbances, even in euthymic phases. Changes in sleep are frequent signs of a new episode of (hypo)mania or depression. Cognitive behavioral therapy for insomnia is an effective treatment for primary insomnia, but has not been introduced to patients with bipolar disorder. The aim is to compare cognitive behavioral therapy added to 'treatment as usual' with just 'treatment as usual'. The investigators hypothesize that cognitive behavioral therapy will improve quality of sleep, stabilize minor mood variations and prevent new mood episodes in euthymic patients with bipolar disorder and insomnia.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date August 2018
Est. primary completion date August 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Fulfilling criteria for SCID-1-verified bipolar I or II disorder

- Euthymic, as defined by Montgomery Åsberg Depression Rating Scale (MADRS) not higher than eleven, and Young Mania Rating scale (YMRS) not higher than five.

- Fulfilling DSM-IV criteria for primary insomnia or insomnia related to another mental disorder, as assessed by the Insomnia Interview Schedule (IIS).

Exclusion Criteria:

- Being or having been in a defined affective episode the last month before inclusion

- Hospitalization in the last two months before inclusion

- Working night shifts

- Sleep apnea

- Medical conditions incompatible with participation.

- Inability to cooperate in the 3-week initial phase before randomization.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive behavioral therapy for insomnia
CBT-I will be given during 3-6 sessions according to need by two therapists being either psychiatrists or psychologists with clinical experience in CBT-I.

Locations

Country Name City State
Norway Østmarka Psychiatric Department, St Olavs Hospital Trondheim

Sponsors (2)

Lead Sponsor Collaborator
Norwegian University of Science and Technology St. Olavs Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in quality of sleep at 8 weeks As assessed by the Insomnia Severity Index (ISI) At 8 weeks from randomization
Primary Change from baseline in quality of sleep at 6 months follow-up As assessed by the Insomnia Severity Index (ISI) 6 months from end of treatment phase
Secondary Variation in sleep registration from baseline to 8 weeks Comparing registrations of sleep by sleep diaries, actigraphs and polysomnography. At 8 weeks
Secondary Variation in sleep registration from baseline to 6 months follow-up Comparing registrations of sleep by sleep diaries, actigraphs and polysomnography. At 6 months
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