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Behavioral and Pharmacological Treatment for Insomnia
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Study NCT00042146   Information provided by National Institute of Mental Health (NIMH)
First Received: July 24, 2002   Last Updated: November 17, 2005   History of Changes

July 24, 2002
November 17, 2005
December 2001
 
 
 
Complete list of historical versions of study NCT00042146 on ClinicalTrials.gov Archive Site
 
 
 
Behavioral and Pharmacological Treatment for Insomnia
Behavioral and Pharmacological Treatment for Insomnia

This study will evaluate the long- and short-term effects of cognitive-behavior therapy (CBT), alone and in combination with zolpidem (Ambien®), for chronic insomnia.

Insomnia is a prevalent health concern which is often associated with functional impairments, reduced quality of life, and increased health-care costs. The proposed study may provide useful information about optimal models for integrating behavioral and pharmacological therapies for the clinical management of insomnia.

Participants are randomly assigned to CBT or CBT plus medication. After the 6-week acute treatment phase, participants enter into a 6-month extended treatment phase. Of those treated with CBT alone initially, responders are randomized to extended CBT or no treatment. Of those receiving the combined CBT plus medication approach initially, responders are randomized to an extended treatment consisting of either CBT plus medication (used on an as needed schedule) or CBT alone (plus medication tapering). Outcome is evaluated across measures of sleep, clinical ratings, and several indices of daytime functioning. The measures are administered at baseline, at the end of the acute and extended treatment phases, and at 6, 12, and 24-month follow-up.

Phase IV
Interventional
Treatment, Randomized, Open Label, Parallel Assignment, Efficacy Study
Sleep Initiation and Maintenance Disorders
  • Behavioral: Cognitive-behavior therapy
  • Drug: zolpidem
 
Morin CM, Vallières A, Guay B, Ivers H, Savard J, Mérette C, Bastien C, Baillargeon L. Cognitive behavioral therapy, singly and combined with medication, for persistent insomnia: a randomized controlled trial. JAMA. 2009 May 20;301(19):2005-15.

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
160
 
 

Inclusion criteria:

  • Subjective complaint of difficulties initiating or maintaining sleep, accompanied by marked distress or daytime impairments due to insomnia
  • Sleep difficulties present 3 nights or more per week and lasting for more than 6 months

Exclusion criteria:

  • Major medical or psychiatric problems
Both
30 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT00042146
 
R01 MH60413, DATR A4-GPS
National Institute of Mental Health (NIMH)
 
 
National Institute of Mental Health (NIMH)
November 2005

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP