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N/A N=97 Randomized Triple-blind Treatment

Brief Interventions for Short-Term Suicide Risk Reduction in Military Populations

Suicide · Suicidal Ideation

Enrolled (actual)
97
Serious AEs
1.0%
Results posted
Aug 2017
Primary outcome: Primary: Estimated Proportion of Participants With Suicide Attempt — 0.19; 0.03; 0.06 estimated proportion of participants — p=.082

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Treatment As Usual (TAU) (Behavioral); Standard Crisis Response Plan (S-CRP) (Behavioral); Enhanced Crisis Response Plan (E-CRP) (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Utah
Primary completion
Sep 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Estimated Proportion of Participants With Suicide Attempt
0.19; 0.03; 0.06 .082
SECONDARY
Beck Scale for Suicide Ideation (BSSI)
8.4; 5.3; 3.5; 5.8; 6.0; 3.3 <0.001 sig
SECONDARY
Inpatient Psychiatric Hospitalization Days
2.5; 0.9; 1.2 <0.001 sig

Summary

The purpose of the proposed study is to identify the most effective brief interventions for reducing short-term risk for suicide attempts in "real world" military triage settings, and to identify potential mechanisms of change underlying the interventions' impact on subsequent suicide attempts. We will randomize 360 patients to one of three commonly-used crisis interventions delivered as routine care in the mental health triage system: (1) Treatment As Usual (TAU); (2) Standard Crisis Response Plan (S-CRP); or (3) Enhanced Crisis Response Plan with Reasons For Living (E-CRP). The following hypotheses will be tested: 1. The enhanced crisis response plan (E-CRP) intervention will contribute to significantly decreased risk for suicide attempts and hospitalization during follow-up relative to the standard crisis response plan alone (S-CRP) and treatment as usual (TAU). 2. The standard crisis response plan (S-CRP) intervention will contribute to significantly decreased risk for suicide attempts and hospitalization during follow-up relative to treatment as usual (TAU). 3. Greater ambivalence about suicide and faster recall of reasons for living will mediate the relationship between intervention and reduced risk for suicide attempt during follow-up.

Eligibility Criteria

Inclusion Criteria

  • Active duty
  • 18 years of age or older
  • Reporting current suicidal ideation with intent to die, or a suicide attempt within the past two weeks
  • Able to speak and understand the English language
  • Able to complete the informed consent process

Exclusion Criteria

  • Severe psychiatric or medical conditions that preclude the ability to provide informed consent or participation in outpatient treatment
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02042131). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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