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Clinical Trials/NCT04084756
NCT04084756
Unknown
Not Applicable

Couples Intervention to Improve Mental Health

Wesleyan University1 site in 1 country200 target enrollmentAugust 1, 2019
ConditionsSuicide

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicide
Sponsor
Wesleyan University
Enrollment
200
Locations
1
Primary Endpoint
Change in suicidal thoughts and behaviors since baseline measured by the Scale for Suicidal Ideation
Last Updated
3 years ago

Overview

Brief Summary

Over the last decade, suicide rates have risen within the military and have remained high. Converging evidence suggests that suicide prevention efforts may be enhanced by explicitly including family members in treatment. The study's objectives are to test the effect of the CCRP, a targeted single session couples intervention on suicide ideation among military service members and Veterans, and to understand how the use of the CCRP impacts suicide risk during the 6 months immediately postdischarge from a psychiatric inpatient unit.

Detailed Description

Over the last decade, suicide rates have risen within the military and have remained high. Converging evidence suggests that suicide prevention efforts may be enhanced by explicitly including family members in treatment, however no couple-bases suicide-specific interventions exist. The study's objectives are to test the effect of the Couples Crisis Response Plan (CCRP), a targeted single-session couples intervention, on suicide ideation among military service members and Veterans, and to understand how the use of the CCRP impacts suicide risk during the period of time immediately post-discharge from a psychiatric inpatient unit. The CCRP will be compared to an active control condition (mental health education). The primary aim is to compare the effect of the CCRP to an active control condition on suicide ideation in the 6 months following treatment among military service members and Veterans who have been psychiatrically hospitalized for acute suicide risk and their partners. The CCRP is specifically adapted for use with partnered service members at elevated risk for suicide. A secondary aim is to determine how use of the CCRP skills impacts suicidal ideation over time and identify the role partners play in encouraging use of the plan and managing suicide risk.

Registry
clinicaltrials.gov
Start Date
August 1, 2019
End Date
September 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Alexis May

Assistant Professor

Wesleyan University

Eligibility Criteria

Inclusion Criteria

  • military service member (active duty or veteran) of any branch or component that has served since 9/11/2001 or the partner of such a service member;
  • that the service member reports active suicide ideation and/or a suicide attempt within the previous 30 days;
  • that the service member is in a committed, exclusive, cohabiting relationship of at least 6 months;
  • the willingness of the service member's partner to participate in research.

Exclusion Criteria

  • a psychiatric condition, medical condition, or cognitive disability/deficit that precludes the ability of either partner to provide informed consent
  • physical aggression within the past year reported by either partner on a behaviorally-anchored screener for moderate to severe partner violence or extreme relationship distress (a score of of less than 9 on the Couples Satisfaction Index-4)
  • inability of either partner to read or speak English

Outcomes

Primary Outcomes

Change in suicidal thoughts and behaviors since baseline measured by the Scale for Suicidal Ideation

Time Frame: Assessed at baseline and 1, 3 and 6-months follow ups

Self-report assessment of severity of suicidal thoughts and behaviors. Items 1-19 are summed (range: 0-38) and higher scores indicate greater suicide severity. Measured at baseline, hospital discharge, and 1, 3, and 6 month follow ups.

Secondary Outcomes

  • Change in number of suicide attempts from baseline(Assessed at baseline and 1, 3 and 6-months follow ups)

Study Sites (1)

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