Can a weekend retreat help prevent suicide in women veterans?
NCT ID NCT07738445
First seen Jul 31, 2026 · Last updated Jul 31, 2026
Summary
This pilot study tests a 3-day retreat program called GRIT, designed for women veterans who have experienced violence. The goal is to see if the retreat is acceptable and feasible, and whether it can improve social functioning as a way to reduce suicide risk. Participants are randomly assigned to either the in-person retreat or a self-guided version of the program. The study will compare outcomes like satisfaction, loneliness, and social functioning between the two groups.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- GRIT, a 3-day in-person group retreat program
- What this could lead to
- If successful, this retreat-based program could offer a new way to reduce suicide risk by improving social connections among women veterans who have experienced violence.
- What could go wrong
- This is a small pilot study, so results may not apply broadly. The program's benefits are uncertain, and participation requires a significant time commitment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 48 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Experienced interpersonal violence as evidenced by endorsement of items 6, 7, 8, 9, or 11 from the Life Events Checklist for DSM-5® 2. Are willing and able to participate in a two overnight, three-day, retreat and complete pre- and post-retreat surveys 3. Are actively engaged in VHA mental healthcare (i.e., have a documented mental health visit with a VA provider within the last 90 days 4. Endorse some difficulties in social functioning as indicated by a score \>2 on at least two items of the social functioning questionnaire 5. Ability to speak, read, and understand spoken English sufficiently well to complete the procedures of the study 6. Have access to a mobile phone or computer device that will enable participation in virtual video sessions Exclusion Criteria: 1. Current suicidal thoughts and intent (using the Columbia Suicide Severity Rating Scale; C-SSRS, (i.e., endorses items 1, 2, and 4 or 5) 2. Diagnosis of alcohol or substance use dependence in medical record. In cases where alcohol or substance use is identified as problematic but not reaching the threshold for diagnosis of SUD dependence, additional consultation with mental health providers and chart review by the PI will be used to determine suitability for participation 3. Current psychosis or mania as indicated by electronic health records, or as identified during baseline administration of Quick SCID
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Providence VA Medical Center, Providence, RI
Providence, Rhode Island, 02908-4734, United States
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VA Connecticut Healthcare System West Haven Campus, West Haven, CT
West Haven, Connecticut, 06516-2770, United States
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VA Connecticut Healthcare System West Haven Campus, West Haven, CT
West Haven, Connecticut, 06516-2770, United States
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