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A Brief Behavioral Sleep Intervention for Depression Among Military Veterans

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01958541
Recruitment Status : Completed
First Posted : October 9, 2013
Last Update Posted : April 26, 2018
Sponsor:
Collaborator:
VA Palo Alto Health Care System
Information provided by (Responsible Party):
Rebecca Ann Bernert, Stanford University

Brief Summary:
This study investigates the impact of brief behavioral insomnia treatment on depressive symptoms among military veterans.

Condition or disease Intervention/treatment Phase
Insomnia Depression Suicidal Ideation Behavioral: Sleep Intervention I Behavioral: Sleep Intervention II Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 77 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Brief Behavioral Sleep Intervention for Depression Among Military Veterans
Study Start Date : March 2013
Actual Primary Completion Date : September 2017
Actual Study Completion Date : September 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Suicide

Arm Intervention/treatment
Experimental: Behavioral Intervention I
This non-medication group treatment (Sleep Intervention I) consists of four 90-minute sessions.
Behavioral: Sleep Intervention I
Insomnia-focused behavioral treatment (4 sessions).

Active Comparator: Behavioral Intervention II
This non-medication group treatment (Sleep Intervention II) consists of four 90-minute sessions.
Behavioral: Sleep Intervention II
Insomnia-focused behavioral treatment (4 sessions).




Primary Outcome Measures :
  1. Suicidal Ideation [ Time Frame: Change from Baseline in Suicidal Ideation at 7 weeks ]

Secondary Outcome Measures :
  1. Insomnia Symptoms [ Time Frame: Change from Baseline in Insomnia Symptoms at 7 weeks ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria
  • Age 18 or older
  • Veteran
  • Insomnia Symptoms
  • Depression

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01958541


Locations
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United States, California
VA Palo Alto Healthcare System
Palo Alto, California, United States, 94304
Stanford University
Stanford, California, United States, 94305
Sponsors and Collaborators
Stanford University
VA Palo Alto Health Care System
Investigators
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Principal Investigator: Rebecca A Bernert, Ph.D. Stanford University
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Responsible Party: Rebecca Ann Bernert, Principal Investigator, Stanford University
ClinicalTrials.gov Identifier: NCT01958541    
Other Study ID Numbers: 22427
W81XWH-10-2-0178 ( Other Grant/Funding Number: Department of Defense )
First Posted: October 9, 2013    Key Record Dates
Last Update Posted: April 26, 2018
Last Verified: April 2018
Keywords provided by Rebecca Ann Bernert, Stanford University:
Sleep
Insomnia
Suicidal Symptoms
Suicidal Ideation
Military Veteran
Service Member
Depression
Additional relevant MeSH terms:
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Sleep Initiation and Maintenance Disorders
Depression
Depressive Disorder
Suicidal Ideation
Behavioral Symptoms
Mood Disorders
Mental Disorders
Sleep Disorders, Intrinsic
Dyssomnias
Sleep Wake Disorders
Nervous System Diseases
Suicide
Self-Injurious Behavior