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Clinical Trials/NCT01958541
NCT01958541CompletedNot Applicable

A Brief Behavioral Sleep Intervention for Depression Among Military Veterans

Stanford University4 sites in 1 country77 target enrollmentStarted: March 2013Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
77
Locations
4
Primary Endpoint
Suicidal Ideation
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Behavioral Intervention I

Experimental

This non-medication group treatment (Sleep Intervention I) consists of four 90-minute sessions.

Intervention: Sleep Intervention I (Behavioral)

Behavioral Intervention II

Active Comparator

This non-medication group treatment (Sleep Intervention II) consists of four 90-minute sessions.

Intervention: Sleep Intervention II (Behavioral)

Outcomes

Primary Outcomes

Suicidal Ideation

Time Frame: Change from Baseline in Suicidal Ideation at 7 weeks

Secondary Outcomes

  • Insomnia Symptoms(Change from Baseline in Insomnia Symptoms at 7 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rebecca Ann Bernert

Principal Investigator

Stanford University

Study Sites (4)

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A Brief Behavioral Sleep Intervention for... | Clinical Trial