Overcontrol and Suicide in PTSD

Completed

Conditions studied: Compulsive Personality Disorder, Stress Disorders, Post-Traumatic

In brief

High standards and self-discipline are prized in military culture, but drawbacks of overcontrol are often ignored. Overcontrol is characterized by over-regulated behavior and cognitive rigidity, driven by an intense need for perfection and control. It is frequently observed in people with obsessive-compulsive (OC) spectrum disorders, especially OC Personality Disorder (OCPD). Their inclination to set high expectations for others can strain social bonds. When grappling with mental health challenges, overcontrolled individuals often do so with limited social support, and as a result, tend to be at greater risk of developing more severe mental health symptoms, or suicidal thoughts and behaviors, over time. New treatments are needed to improve social functioning in these vulnerable Veterans. Adding brain stimulation to psychotherapy is one method that might speed learning of social skills discussed in therapy. However, before this technology can be developed and tested more broadly, the investigators must make sure that the methods used to measure social functioning and related brain circuits are acceptable to most potential patients and can be used consistently. In this pilot project, the investigators aim to recruit trauma-exposed Veterans with overcontrolled traits and study the feasibility and acceptability of: 1. Our recruitment strategy and social functioning and mental health symptom assessments 2. A three-session, weekly fMRI protocol. 3. A three-week online protocol for remote monitoring of social and emotional functioning.

Key facts

Study ID

NCT06355284

Run by

VA Office of Research and Development

People needed

59

Starts

2024-07-01

Expected to finish

2026-04-30

Last updated by the study team

2026-07-07

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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).

You may not qualify if…

• 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.

Where it is running

• Providence VA Medical Center, Providence, RI — Providence, Rhode Island, United States

Full record on ClinicalTrials.gov

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