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Nonpharmacologic Group Treatment of Secondary Insomnia - Article


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Insomnia


Clinical Trial: Nonpharmacologic Group Treatment of Secondary Insomnia

This study is not yet open for patient recruitment.
Verified by Norwegian University of Science and Technology October 2005

Sponsored by: Norwegian University of Science and Technology
Information provided by: Norwegian University of Science and Technology
ClinicalTrials.gov Identifier: NCT00235365

Purpose

The purpose of this study is to determine the effect of nonpharmacologic group treatment for patients with secondary insomnia.
Condition Intervention
Secondary Insomnia
 Behavior: Education about sleep and sleep hygiene
 Behavior: cognitive therapy
 Behavior: Sleep restriction
 Behavior: Relaxation techniques

MedlinePlus related topics:  Sleep Disorders

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study

Official Title: Nonpharmacologic Group Treatment for Patients With Psychiatric Disorders and Insomnia

Further study details as provided by Norwegian University of Science and Technology:
Primary Outcomes: Scores on rating scales for sleep quality
Secondary Outcomes: Scores on rating scales for depression, psychiatric symptom severity, and cognitive processing.
Expected Total Enrollment:  40

Study start: October 2005;  Expected completion: December 2008
Last follow-up: December 2007;  Data entry closure: December 2008

This study is a randomized controlled trial with 40 paitents with a psychiatric disorder and insomnia. The patients will be randimized into two groups of 20 patients. The first group recieve group therapy immediately, whereas the second group will be assigned to a waiting list control for five weeks before they also receive group therapy. The patients will be given six sessions of group therapy, twice a week for three weeks. The main topics will be: education about sleep and sleep hygiene, cognitive therapy, stimulus control, sleep restriction, and relaxation techniques.

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • Insomnia secondary to a primary psychiatric disorder

Exclusion Criteria:

  • substance abuse, psychotic symptoms, suicidal intentions, severe organic disorder or psychiatric disorder where sleep restriction is not adviced, organic sleep disorder.

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00235365

Knut Langsrud, Psychiatrist      +4773864500    knut.langsrud@ntnu.no
Bjarne Hansen, Psychologist      +4773864604    bjarne.hansen@ntnu.no

Norway
      Norwegian University of Science and Technology, Institute of Neuroscience, Trondheim,  Norway
Knut Langsrud, Psychiatrist  +4773864500    knut.langsrud@ntnu.no 
Bjarne Hansen, Psychologist  +47738664500    bjarne.hansen@ntnu.no 

Study chairs or principal investigators

Gunnar Morken, PhD MD,  Principal Investigator,  Norwegian University of Science and Technology   

More Information

Study ID Numbers:  S2005.2.gr
Last Updated:  December 8, 2005
Record first received:  October 7, 2005
ClinicalTrials.gov Identifier:  NCT00235365
Health Authority: Norway: Norwegian Social Science Data Services
ClinicalTrials.gov processed this record on 2006-01-10


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Page Updated: May 11, 2006
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