Actively Recruiting

Phase Not Applicable
Age: 16Years +
All Genders
Healthy Volunteers
ID06582953

Advancing the Evidence for HVIPs in the Southeast: Comprehensive Patient-Centered Outcomes and Stakeholder Insights

Led by Medical University of South Carolina · Updated on 2026-04-09

220

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

Sponsors

M

Medical University of South Carolina

Lead Sponsor

K

Kaiser Permanente

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the Turning the Tide Violence Intervention Program (TTVIP), a hospital violence intervention program (HVIP) at a Southeastern academic trauma center. The study focuses on youth and young adults injured by community and interpersonal violence, primarily firearm injuries, in Charleston and nearby counties. It aims to understand comprehensive outcomes beyond injury recurrence, including healthcare experiences, mental health, violence risk, self-confidence, and stakeholder perspectives from patients, families, and healthcare providers. The program is integrated into routine care for patients aged 15 to 35 treated at the hospital who have experienced violent injuries or are at high risk. Participants may choose to receive services from TTVIP, which provides immediate support, communication assistance, anti-retaliation messaging, and long-term mentorship and referrals for services like education, employment, substance abuse treatment, injury recovery, housing, and mental health over up to one year. Family members and healthcare providers involved in care are also included to assess the program's broader impact. Participants will be assessed over time at enrollment and at 3, 6, and 12 months after for outcomes such as PTSD symptoms, depression, self-esteem, firearm violence risk, recovery service needs, repeat injuries, and perceptions of care quality. Surveys and assessments will also capture perceived benefits from the perspectives of patients, loved ones, and healthcare staff. The study will collect data to inform improvements and understand the program's effects in communities with high firearm violence. The research will continue until November 2027.

CONDITIONS

Brief Title

HVIP Outcomes and Stakeholder Insights

Who Can Participate

Age: 16Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 16 and above treated at MUSC Charleston with injuries from interpersonal or community violence
  • Glasgow coma score of 15 at enrollment
  • Loved ones, caregivers, and family members of enrolled patients
  • Healthcare team members who cared for victims of violence in the past 6 months
Not Eligible

You will not qualify if you...

  • Unable to consent due to altered mental status or severe untreated mental illness
  • Currently under arrest or incarcerated
  • Non-English speaking patients, loved ones, or caregivers
  • Patients under age 16
  • Loved ones or caregivers with cognitive impairment or under age 16

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Up to 1 year after injury

Participants who have experienced violent injuries receive services from the hospital violence intervention program integrated into their regular care, including immediate support, mentorship, service referrals, and mental health services for up to one year after injury.

Baseline enrollment and follow-up assessments at 3 months, 6 months, and 12 months

Long-term Monitoring

Duration - Up to 1 year after injury

Participants' health outcomes, violence risk, mental health, and service utilization are monitored over time to assess the benefits and impact of the intervention and standard care.

Assessments at baseline, 3 months, 6 months, and 12 months after enrollment

Trial Site Locations

Total: 1 location

1

Medical University of South Carolina

Charleston, South Carolina, United States, 29407

Actively Recruiting

Loading map...

Research Team

A

Ashley Hink, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

Similar Trials

BeSMART Secure Storage Counseling in the Inpatient Setting t...

Firearm Injury

Actively Recruiting

2 locations

Community Resiliency Collective Efficacy Intervention (CRCEI...

Violence, Physical

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

A descriptive exploration of the geographic and sociodemographic concentration of firearm homicide in the United States, 2004-2018.

Scott R Kegler, Linda L Dahlberg, Alana M Vivolo-Kantor

https://pubmed.ncbi.nlm.nih.gov/34416223