Clinical trial Recruiting at 1 site Phase 2 Interventional Ages 18 and up

Comparing psychotherapy treatments for suicide risk in Veterans

Official title: Suicide Risk Interventions: A Comparison of Treatment Dose and Neural Markers of Treatment Outcome

Run by VA Office of Research and Development · NCT05931289 · Data updated 2026-11-12

This study is testing two different therapy options for Veterans who have been hospitalized for suicide risk to see which one helps them cope better and reduces their suicidal thoughts.

More Suicide trials

Quick facts

PhasePhase 2
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment136 (estimated)
SponsorVA Office of Research and Development
Federal
Locations1 site (Boston, Massachusetts)
StatusRecruiting
StartedMarch 3, 2025
Main results expectedDecember 31, 2027
Study endsDecember 31, 2027
Registry record updatedFebruary 17, 2026
Trial IDNCT05931289 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are Veterans who have recently been hospitalized for a suicidal crisis and are willing to participate in outpatient therapy sessions.

Probably not a fit

Patients with significant cognitive impairment or current psychotic or manic features 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 study aims to evaluate the effectiveness of two different psychotherapy treatments for Veterans who have been hospitalized due to suicide risk. Participants will be randomly assigned to receive either Enhanced Crisis Response Planning (ECRP) or Brief Cognitive Behavioral Therapy for Suicide Prevention (BCBT) after their hospital discharge. The study will assess whether a longer duration of therapy leads to better coping skills and reduced suicidal thoughts, particularly focusing on Veterans with a history of multiple suicide attempts. Additionally, neuroimaging scans will be conducted to explore the neurobiological mechanisms associated with suicide risk.

Why it matters

Potential benefit: If successful, this study could lead to more effective psychotherapy interventions that significantly reduce suicide risk among Veterans.

How similar studies have gone: Previous studies have shown that both ECRP and BCBT can reduce suicide attempts, but this direct comparison of their effectiveness is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* hospitalization for a recent suicidal crisis consisting of SI with intent to die within the past week and/or a suicide attempt within the past month
* Veteran status
* ability to speak English
* ability to complete the informed consent process
* willingness/ability to attend 12 outpatient treatment sessions and 3 fMRI sessions following hospital discharge

Exclusion Criteria:

* significant cognitive impairment
* current psychotic or manic features

Where it's running

  • VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
    Boston, Massachusetts, United States
    Recruiting

Study contacts

  • Principal investigator: Michael S Esterman, PhD — VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
  • Study coordinator: Michael S Esterman, PhD
  • Email: Michael.Esterman@va.gov
  • Phone: (857) 364-4362

Similar studies

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

  • Friends and family training for those at risk of suicide

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    Recruiting Unity Health Toronto · Toronto, Ontario · NCT07902089

  • Inhaled DMT for major depressive disorder

    This trial tests whether inhaled DMT can quickly ease depressive symptoms and reduce suicide risk in adults with major depressive disorder.

    Recruiting Phase 2 Universidade Federal do Rio Grande do Norte · Fortaleza, Ceará and 4 other locations · NCT07562191

  • Suicide risk and learned suicide ability in people with mood disorders

    This project will try to identify which biological, psychological, social, and clinical factors relate to suicide risk and the learned ability for suicide in people aged 16–60 with mood disorders by collecting blood, urine, and questionnaire data.

    Recruiting Tianjin Anding Hospital · Tianjin, Tianjin Municipality · NCT07523490

  • Combining the Youth-Nominated Support Team with CBT for Black adolescents at acute suicide risk

    This project will test whether adding a computer-assisted Youth-Nominated Support Team to Cognitive Behavioral Therapy for Suicide Prevention helps Black adolescents (ages 12-17) who come to an urban emergency setting with suicidal thoughts or self-injury.

    Recruiting at 2 sites University of Michigan · Detroit, Michigan and 1 other locations · NCT07506460

  • Remote case management to prevent suicide after psychiatric hospital discharge

    This project will test whether a 6-month remote program called Pathfinding helps active-duty Army soldiers reduce suicidal behavior after leaving inpatient psychiatric care.

    Recruiting Uniformed Services University of the Health Sciences · Bethesda, Maryland · NCT07404787

  • Text reminders to help parents keep teens safe after a suicide-related ED visit

    This study tests whether sending parents text messages can help them reduce their teen’s access to lethal means and increase safety practices after a suicide-related emergency visit.

    Recruiting University of Texas Southwestern Medical Center · Dallas, Texas · NCT07383714

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.