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A Brief Intervention to Reduce Suicide Risk in Military Service Members and Veterans- Study 1

A Brief Intervention to Reduce Suicide Risk in Military Service Members and Veterans- Study 1

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01334541
Acronym
SAFE VET
Enrollment
600
Registered
2011-04-13
Start date
2009-09-30
Completion date
2018-12-31
Last updated
2019-01-31

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

Conditions

Suicide Risk | Patient

Brief summary

The investigators propose to evaluate Suicide Assessment and Follow-up Engagement: Veteran Emergency Treatment (SAFE VET) which is currently being implemented in 4 VA ED/Urgent Care Units across the United States (Portland VA Medical Center (VAMC), Denver VAMC, Manhattan VAMC, and Philadelphia VAMC).

Detailed description

Background: In 2009, a novel clinical demonstration project entitled Suicide Assessment and Follow-up Engagement: Veteran Emergency Treatment (SAFE VET) was initiated as a potential standard of care for suicidal Veterans who receive treatment at Veterans Affairs (VA) emergency departments (ED). SAFE VET is designed to attenuate suicide risk by helping Veterans manage suicidal thoughts and behaviors, and adhere to prescribed clinical care; thereby promoting resiliency and increased capacity to cope with suicidal states. Objectives: Using a quasi-experimental design, the aim of this study is to compare the effectiveness of the SAFE VET intervention versus enhanced usual care (E-CARE)on the following: 1) the proportion of patients who attempt suicide within 6 months of index emergency department (ED) visit; 2) the severity of suicide ideation within 6 months after index ED visit; 3) the proportion of patients who attend \> 1 outpatient mental health or substance abuse treatment appointments within 30 days following index ED visit; and 4) the degree of suicide-related coping for attending treatment during the 6 month period. Methodology: Six hundred Veterans, up to 300 per condition (SAFE VET or E-CARE), who meet inclusion/exclusion criteria will be enrolled. E-CARE sites are as follows: Long Beach VAMC, Bronx VAMC, Milwaukee VAMC, and San Diego VAMC. All subjects will participate in an approximately 1-hour long baseline assessment battery (index ED visit) by phone, and will be contacted by phone at approximately 1, 3, and 6 months after the index ED visit to complete follow-up measures. Medical records will also be reviewed to determine VA health service usage in the six-month period after study enrollment.

Interventions

BEHAVIORALSAFE VET

All SAFE VET EDs provide a standardized intervention that is specifically adapted for use in the ED to mitigate suicide risk. Given that the SAFE VET intervention was developed for use in a busy ED setting, the length of the intervention is approximately 45 minutes. The SAFE VET intervention is administered by a clinical provider who has been specifically trained and consists of: 1. Risk Assessment 2. Safety Planning Intervention: Developed by Stanley and Brown (2008), Safety Planning Intervention consists of a hierarchically-arranged list of coping strategies identified for use during a subsequent suicidal crisis. 3. Clinical Follow-Up Protocol

Sponsors

US Department of Veterans Affairs
CollaboratorFED
United States Department of Defense
CollaboratorFED
Columbia University
CollaboratorOTHER
University of Pennsylvania
CollaboratorOTHER
Uniformed Services University of the Health Sciences
CollaboratorFED
VA Eastern Colorado Health Care System
Lead SponsorFED

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

Veterans will be enrolled who: 1. have received the SAFE VET intervention in VA SAFE VET EDs or treatment-as-usual in E-CARE EDs; 2. aged 18 years or older; 3. identified as being at risk for suicide based upon presenting complaints and/or the assessment of an ED clinician; 4. able to provide 2 contacts with telephone numbers for tracking purposes; and 5. able to provide a home/residential/shelter address where the participant resides and either a home, cellular, or other telephone number where the participant can be reached.

Exclusion criteria

Veterans will not be enrolled if they are: 1. unable to read and understand English; 2. unable or unwilling to give informed consent as determined either by the referring VA ED clinical staff or research personnel (see Mini Quiz below); and/or 3. admitted to the VA inpatient psychiatric unit from the ED.

Design outcomes

Primary

MeasureTime frame
Columbia Suicide-Severity Rating Scale (C-SSRS; Posner et al., 2006; Posner et al. 2008).Baseline and 1, 3, and 6 month follow-up assessments

Secondary

MeasureTime frame
Scale for Suicide Ideation (SSI; Beck, Kovacs, & Weissman, 1979).Baseline and 1, 3, and 6 month follow-up assessments

Countries

United States

Outcome results

None listed

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