Veterans' brain scans could unlock new suicide prevention strategies
NCT ID NCT06355284
First seen Jun 25, 2026 · Last updated Jul 08, 2026 · Updated 3 times
Summary
This pilot study uses functional MRI to examine brain activity in trauma-exposed veterans with obsessive-compulsive personality traits, known as overcontrol. Overcontrol can strain relationships and increase suicide risk. The study aims to test whether the brain scanning methods and remote monitoring tools are practical and acceptable for future research. If the methods work, they could help develop new treatments that combine brain stimulation with therapy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Functional MRI (brain scanning during cognitive tasks)
- What this could lead to
- If successful, this study could pave the way for new treatments that combine brain stimulation with therapy to improve social skills and reduce suicide risk in veterans.
- What could go wrong
- This is a very early pilot study with only 59 participants, focused on testing methods, not treatment. The results may not apply to all veterans or lead directly to new therapies.
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.
- Participants
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59 people
The number who actually took part.
- Started
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Jul 2024
- Finished
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Apr 2026
- 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.
Who is studied
The study population will include Veterans 18-65 years old. They will be men or women from the greater Providence area receiving care at the VA who have been discharged from active duty, or who served in the National Guard or reserve units. Over 15 months, the investigators plan to screen 74 Veterans aged 18-65 receiving care in VAPHS's Trauma Recovery Clinic (TRC) and Women's Health Clinic (WHC), the latter included to boost female participation.
- Ages
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18 to 65 years
- Sex
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Anyone
- 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: General Inclusion: * All prospective participants must be able to comprehend the study's procedures and associated risks and be capable of providing informed consent. * Mean scores on at least three subscales of the Pathological Obsessive Compulsive Personality Scale (POPS) must be greater than an average score of four (4 = "slightly agree") across subscale items. * The POPS is a 49-item self-report assessment of maladaptive behaviors and thought patterns associated with OCPD. * While Veterans with primary psychotic disorders will be excluded, the presence of other disorders related to obsessive-compulsive tendencies or personality will not be grounds for exclusion. * Psychiatric medication usage will be assessed during enrollment, but this will not serve as an inclusion or exclusion criterion (with an additional stipulation outlined below for the MRI subsample). Exclusion Criteria: General Exclusion: * The Mini International Neuropsychiatric Interview (M.I.N.I.) will be used to exclude participants with current psychosis or with past psychosis that was unrelated to depression. Additional MRI Criteria: * Participants interested in taking part in the MRI portion of the study will undergo a thorough screening to ensure MRI compatibility (e.g., absence of metal in the body, absence of claustrophobia). * Interested participants must meet the following additional criteria: * no medical contraindications for MRI (e.g., pacemakers, non-MRI safe implanted devices) * absence of neurological disorders * no moderate-to-severe traumatic brain injury (e.g., head trauma with loss of consciousness \>5 minutes) * no ongoing poorly controlled substance use disorder. * Lifetime history of seizures, primary or secondary CNS tumors, stroke, or cerebral aneurysm will also be exclusionary. * For participants in the MRI segment of the study, continued medication use will not be a disqualifying factor if the medication regimen has remained stable for the past month, with no intentions of altering dosages during the study duration. * This medication criterion will not be applied to participants who do not complete MRI scans. * For this feasibility trial, individuals exhibiting active suicidal behavior or a score \>3 on the suicidal ideation module of the Columbia-Suicide Severity Rating Scale will be ineligible.
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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.
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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Other studies related to the condition(s) this trial covers.
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