Clinical trial Recruiting at 1 site Interventional Ages 16 and up

Evaluation of a hospital violence intervention program

Official title: Advancing the Evidence for HVIPs in the Southeast: Comprehensive Patient- Centered Outcomes & Stakeholder Insights

Run by Medical University of South Carolina · NCT06582953 · Data updated 2026-11-12

This study is testing a program designed to help young people aged 16-35 who have experienced violence to see if it can reduce repeat injuries, improve their mental health, and enhance their overall hospital experience.

Quick facts

Study typeInterventional
Ages16 Years and up
SexAll
Enrollment220 (estimated)
SponsorMedical University of South Carolina
Academic / other
Locations1 site (Charleston, South Carolina)
StatusRecruiting
StartedDecember 5, 2024
Main results expectedSeptember 30, 2027
Study endsNovember 30, 2027
Registry record updatedApril 9, 2026
Trial IDNCT06582953 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients aged 16-35 treated for injuries due to interpersonal or community violence at MUSC Charleston.

Probably not a fit

Patients who are non-English speaking, under 15 or over 35, or lack the capacity to consent due to mental health issues 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 evaluates the effectiveness of the Turning the Tide Violence Intervention Program at a Southeastern hospital, focusing on patient outcomes and stakeholder insights. It aims to assess how the program impacts violent injury recidivism, PTSD symptoms, and overall healthcare experiences for patients aged 16-35 who have suffered from violence. Additionally, the study seeks to gather perspectives from patients, family members, and healthcare providers to identify potential improvements and benefits of the program. By exploring these dimensions, the research aims to enhance the implementation and understanding of HVIPs in under-studied communities.

Why it matters

Potential benefit: If successful, this study could lead to improved outcomes for patients affected by violence, including reduced recidivism and enhanced support services.

How similar studies have gone: Other studies have shown success with hospital violence intervention programs, but this evaluation focuses on under-studied communities in the Southeast, making it a novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria (patients):

* Patients ages 16 and above treated at MUSC Charleston that experience an injury due to interpersonal or community violence
* Glasgow coma score (GCS) of 15 at the time of study enrollment

Exclusion Criteria (patients):

* Lack of capacity to consent due to altered mental status (AMS) or severe untreated mental illness
* Being under arrest or incarcerated at the time of assessment for enrollment
* Non-English speaking patients
* Ages under 16

Inclusion Criteria (loved ones/caregivers):

-Loved ones (partners), caregivers and family members of patients that enroll in the study that experienced violent injuries

Exclusion Criteria (loved ones/caregivers):

* Non-English speaking
* Cognitive impairment
* Under age 16

Inclusion Criteria (Healthcare Providers):

-Healthcare team members that cared for victims of violence in the past 6 months

Where it's running

  • Medical University of South Carolina
    Charleston, South Carolina, United States
    Recruiting

Study contacts

  • Principal investigator: Ashley Hink, MD — Medical University of South Carolina
  • Study coordinator: Ashley Hink, MD
  • Email: hink@musc.edu
  • Phone: 843-792-7082

Similar studies

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

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.