About this trial
This clinical trial is designed to evaluate the effectiveness of three interventions aimed at preventing violence and supporting those affected by it. Over next three years, the impact of these interventions on key areas will be measured, including the incidence of firearm injuries, the recovery of victims, the occurrence of retaliation and re-injury, and health economics. The interventions are developed based on data collected from a comprehensive needs assessment, community summit, retrospective medical chart reviews, and focus group sessions. The defined interventions are as follows:
Intervention A - Integration of an existing community-based intervention program with Hospital services intervention B - Unrestricted Cash Assistance Intervention C - Mobile Community Support Services
Additionally, the investigators will implement a detailed violence-focused survey for firearm survivors at the time of study enrollment. Follow-up is planned at 3,6 and 12 months. The results of this trial (including analyses of firearm injury rates, recovery outcomes, retaliation/re-injury occurrences, and economic data) will be shared with the affected communities and stakeholders to promote ongoing improvement and support.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 18 years or older
Firearm injury within the last 24 hours prior to their arrival at the University of Mississippi Medical Center
Residency/home address within one of the designated clusters.
Be approached by the research team within 72 hours of arrival.
Disqualifiers
Self-inflicted gunshot wounds
Less than 18 years of age
Patients who are incarcerated or in-custody
Patients who are unable to understand the clinical trial or sign consent (whether from intoxication, injury, or other cause)
Trial design
Sequential
Treatments tested in this trial
Hospital-Linked Violence Intervention Program
BehavioralActivation of Operation Good, our community partner with a history of direct violence interruption in the streets and longitudinal health and wellness services to firearm injured patient (i.e. linking and aiding those who have suffered from violent injury to mental healthcare, job services, educational services)
Mobile Community Event Support
BehavioralA menu of services provided to the community in an activated cluster where funding will be provided to assist that community in holding events that support overall health and wellness (community clean-up, legal advisory services, pop-up clinic for blood pressure checks).
Unrestricted Cash Assistance
BehavioralA participant in an activated cluster after firearm injury will receive two disbursements of 500$. One at the time of initial hospital evaluation and a second disbursement \~1 month later to offset the financial burden associated with firearm injury on the individual.
Treatment groups
Trial outcomes
Primary outcomes
Incidence of death and gunshot injuries
The data will be collected from hospital and JPD records. Excluding self-inflicted such as suicide or adjudicated to be accidental/unintentional.
Secondary outcomes
Incidence of PTSD, Score of perceived stress and social cohesion
Individual level longitudinal measure and includes "incidence of PTSD, score of perceived stress and social cohesion" collected by individual level surveys.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
University of Mississippi Medical Center
Lead sponsor
National Institutes of Health (NIH)
Collaborator
National Institute on Minority Health and Health Disparities (NIMHD)
Collaborator
This trial is not recruiting at the moment. You can still explore other options: