Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Web-based intervention for reducing suicidal thoughts in veterans

Official title: Effects of a Targeted Web-Based Suicide Prevention Intervention on Suicidal Ideation and Self-Directed Violence: A Randomized Controlled Trial in Veterans

Run by VA Office of Research and Development · NCT05884476 · Data updated 2026-11-12

This study tests a web-based program that helps veterans learn skills to manage suicidal thoughts and see if it works better than regular healthcare visits.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment180 (estimated)
SponsorVA Office of Research and Development
Federal
Locations1 site (New Orleans, Louisiana)
StatusRecruiting
StartedJanuary 8, 2024
Main results expectedJune 30, 2027
Study endsJune 30, 2027
Registry record updatedDecember 18, 2025
Trial IDNCT05884476 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are veterans aged 18 and older who have experienced suicidal thoughts in the past two weeks.

Probably not a fit

Patients with active psychosis, unmedicated bipolar disorder, or those requiring inpatient detoxification for substance use disorders may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to evaluate a web-based intervention designed to help veterans cope with suicidal thoughts by teaching them adaptive skills to manage emotional distress. The intervention lasts approximately 40 minutes and will be compared to standard healthcare visits to assess its effectiveness in reducing suicidal ideation and behaviors. The study will measure changes in suicidal thoughts and behaviors over the course of one month, focusing on the unique needs of veterans who experience these challenges. By directly addressing psychological inflexibility, the intervention seeks to provide a more accessible and effective approach to suicide prevention.

Why it matters

Potential benefit: If successful, this intervention could significantly reduce suicidal thoughts and behaviors among veterans, improving their overall mental health and well-being.

How similar studies have gone: While there have been few existing interventions targeting psychological inflexibility in suicidality, this approach is relatively novel and aims to expand access to effective suicide prevention strategies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Veteran
* 18 years or older
* Past two-week suicidal ideation as indicated by positive reply to C-SSRS questions ("Have you had any actual thoughts of killing yourself," or, "Have you been thinking about how you might do this?")

Exclusion Criteria:

* Active psychosis
* Unmedicated bipolar disorder
* Instances in which a substance use disorder would indicate inpatient detoxification prior to engaging in other outpatient mental health interventions

Where it's running

  • Southeast Louisiana Veterans Health Care System, New Orleans, LA
    New Orleans, Louisiana, United States
    Recruiting

Study contacts

  • Principal investigator: Joseph W Boffa, PhD — Southeast Louisiana Veterans Health Care System, New Orleans, LA
  • Study coordinator: Joseph W Boffa, PhD
  • Email: joseph.boffa@va.gov
  • Phone: (504) 507-2000

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.