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Evaluation of a Trauma-Informed Partner Violence Intervention Program

StatusEnrolling by Invitation
PhaseNot applicable
Started
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Record History

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  1. Enrollment increased: 800 → 1000 participants
  2. Secondary endpoints: details revised at 4 of 4 entries
    • Study description expanded, about 7 words
    • Site details revised
    • Eligibility criteria expanded, about 2 words
  3. Study sites: 2 to 1
    • Collaborators: 2 to 1
    v7
  4. Re-verified, no change to tracked fieldsv6
  5. Trial status: Recruiting to Enrolling by Invitation
    • Start date changed from estimate of Apr 2025 to Feb 13, 2025
    • Site details revised at 2 of 2 sites
    v5
Show 3 earlier versionsHide 3 earlier versions
  1. Trial status: Not Yet Recruiting to Recruiting
    • Site details revised at 2 of 2 sites
    v4
  2. Start date: Feb 2025 to Apr 2025v3
  3. Study title shortened, about 4 wordsv2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Boston University
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PTSD
889 trials monitored
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The goal of this study is to conduct a randomized controlled trial (RCT) comparing outcomes between two programs to reduce intimate partner violence (IPV)- the Strength at Home (SAH) program and a standard, state-approved IPV intervention program, Treatment as Usual (TAU). Primary outcomes will include self- and partner-reported physical and psychological IPV. Secondary outcomes will include self-reported PTSD symptoms, alexithymia, alcohol use problems, and treatment satisfaction, assessed across five time points.
Trial Details
NCT Number NCT06803043
Lead Sponsor Boston University
Collaborators: Patient-Centered Outcomes Research Institute
Conditions
(from sponsor)		 Domestic Violence, Post Traumatic Stress Disorder
Related terms Affective Symptoms, Alcohol Drinking, Stress Disorders, Post-Traumatic
Enrollment 1,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov