Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06596044

Suicide Prevention After Community Care Discharge

Led by VA Office of Research and Development · Updated on 2026-04-24

120

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

V

VA Office of Research and Development

Lead Sponsor

W

White River Junction Veterans Affairs Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

The study is of high importance to Veterans' health because it will study a suicide prevention intervention in a Veteran population that is at high risk of suicide but has not been a specific focus of the Veteran Affairs' (VA's) suicide prevention efforts. Specifically, a growing number of Veterans are now receiving acute mental health treatment in VA-purchased settings (commonly referred to as Community Care). While these Veterans are at high risk of suicide after discharge, very little is known about how to prevent suicide in these Veterans. This study will directly address this problem by looking at whether a promising suicide prevention strategy called the VA Brief Intervention and Contact Program (VA BIC) can decrease the risk of suicide in Veterans after they are discharged from a non-VA mental health treatment setting. The proposed research is highly pertinent to the VA's top clinical priority-to prevent suicide in Veterans.

CONDITIONS

Official Title

Suicide Prevention After Community Care Discharge

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Veteran who is eligible to receive VA services
  • 18 years or older
  • Able to speak English
  • Received acute psychiatric treatment in a non-VA setting affiliated with VA in Northern New England
  • Endorsed recent suicidal ideation (score 2 or higher on Beck Scale for Suicidal Ideation)
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Currently receiving assertive community treatment
  • Belongs to potentially vulnerable populations such as prisoners, institutionalized patients, or patients admitted under involuntary commitment
  • Deemed clinically inappropriate by study physician due to clinical status such as active psychosis or dementia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

White River Junction VA Medical Center, White River Junction, VT

White River Junction, Vermont, United States, 05001-3833

Actively Recruiting

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Research Team

N

Natalie Riblet, MD MPH

CONTACT

B

Bradley V Watts, MD MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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