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A Brief Intervention to Reduce Suicide Risk in Military Service Members and Veterans - Study 2 (SAFEMIL)

A Brief Intervention to Reduce Suicide Risk in Military Service Members and Veterans - Study 2

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01360736
Acronym
SAFEMIL
Enrollment
102
Registered
2011-05-26
Start date
2009-09-30
Completion date
2018-12-31
Last updated
2020-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide, Suicide, Attempted

Keywords

Suicide Prevention, Suicide Attempt, Suicide Ideation, Randomized Controlled Trial, Safety Planning

Brief summary

The investigators propose to test the efficacy of a brief, readily accessible, and personalized treatment called the Safety Planning for Military (SAFE MIL; Stanley and Brown, 2012).

Detailed description

Background: Mental health related hospitalizations and suicide are both significant public health problems within the United States Department of Defense (DoD). There are limited evidence-based suicide prevention interventions that have been developed for military personnel and veterans who are experiencing suicide ideation or who have made a suicide attempt. Objectives: To evaluate the efficacy of the Safety Planning for Military (SAFE MIL) on suicide ideation, suicide-related coping, and attitudes toward help seeking for hospitalized military personnel at high suicide risk. Methodology: To test the efficacy of the adapted intervention, the investigators will randomize 186 patients to one of two conditions: Safety Planning for Military (SAFE MIL) or Enhanced Usual Care (E-CARE). The SAFE MIL condition (intervention) will consist of the Safety Planning Intervention to help the suicidal individual with a collaboratively generated personal plan to mitigate or prevent a future suicidal crisis. The E-Care will consist of the usual care patients receive at an inpatient facility during their hospitalization in addition to assessment services provided by independent evaluators who work directly with our research team. Primary outcomes include suicide ideation, suicide-related coping, and attitudes toward help-seeking \[acceptability and initiation of services\]. Patients in both conditions will be assessed on the dependent measures at the time of hospital admission (i.e., baseline), at the time discharge (Follow-Up Interval 1 \[FU-1\]), at 1-month (Follow-Up Interval 2 \[FU-2\]) and at 6-month (Follow-Up Interval 3 \[FU-3\]).

Interventions

BEHAVIORALSafety Planning - Military (SAFE MIL)

The Safety Planning Intervention (SPI) which is delivered in the SAFE MIL condition aims to help individuals lower their imminent suicide risk by having them collaborate with the study clinician to generate a detailed, hierarchically-arranged action plan for managing suicidal thoughts and urges.

Sponsors

U.S. Army Medical Research and Development Command
CollaboratorFED
United States Department of Defense
CollaboratorFED
US Department of Veterans Affairs
CollaboratorFED
University of Pennsylvania
CollaboratorOTHER
University of Rochester
CollaboratorOTHER
Columbia University
CollaboratorOTHER
Henry M. Jackson Foundation for the Advancement of Military Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Patient Admitted Due to Recent Suicide Intent and/or Suicide Attempt within past month * Baseline Assessment Completed within 48 Hours of Hospital Admission * Age of 18 years or older.

Exclusion criteria

* Medical Incapacity to Participate and/or Serious Cognitive Impairment * Expected Discharge within 72 Hours of Admission * Expected Deployment within 1-Month * Inability to read or understand English * Inability to provide Informed Consent

Design outcomes

Primary

MeasureTime frameDescription
Suicide Ideationdischarge, 1 month, and 6 months post-dischargeSuicide ideation will be measured using the Columbia Suicide Severity Rating Scale (C-SSRS) and the Scale for Suicide Ideation (SSI). Both measures assess for presence, intensity, frequency, and specificity of suicide related thoughts (ideations).
Acceptability and Initiation of Mental Health Care and Substance Use Treatmentdischarge, 1 month, and 6-months post-dischargeAttitudes toward help-seeking \[acceptability and initiation of services\] will be assessed by the following measures: Attitudes Toward Seeking Professional Psychological Help Scale: modified shortened version (ATSPPH); Cornell Services Index (CSI); Perceived Barriers to Care (PBTC); Brief SAFE MIL Intervention Survey.
Suicide-related Copingdischarge, 1 month, and 6 months post-dischargeCoping strategies will be measured using a checklist of tactics and coping strategies used by individuals to cope with suicidal thoughts, feelings, and urges.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026