The HVIP+ Community Model
Purpose
The present study will use an optimization randomized control trial design to test the preliminary efficacy of a Hospital-based Violence Intervention Program (HVIP) in Central Arkansas.
Conditions
- Hospital-based Violence Intervention
- Community Firearm Violence
- Firearm Behaviors
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Be at least 18 years of age or older - Currently live in Central Arkansas - Currently being treated for a penetrating gun assault injury at a local hospital
Exclusion Criteria
Participants must not: - Report any medical problems that would limit their ability to express thoughts and answer questions (i.e. active intoxication, developmental delays, dementia, psychosis, etc.) - Be currently under arrest or in police custody
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Factorial Assignment
- Intervention Model Description
- The optimization randomized control trial design will entail a factorial experiment with eight experimental conditions to test the targeted outcomes. The eight conditions will include various combinations of four intervention components (brief bedside, peer support, case management, and group therapy), with the brief bedside serving as the constant and the other components being on or off across conditions. Additionally, we will maintain a hybrid effectiveness implementation approach by assessing health outcomes along with implementation outcomes.
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
- Masking Description
- Interventionists (peer community health workers, case managers) will only know which participants are assigned to their intervention component. Only the UAMS PI and research staff will know the interventions assigned to each participant.
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental BB, CM, G |
Participants receive brief bedside, case management+ voucher, and SELF group intervention components. |
|
|
Experimental BB, CM |
Participants receive brief bedside and case management+ voucher intervention components. |
|
|
Experimental BB, G |
Participants receive brief bedside and SELF group intervention components. |
|
|
Experimental BB |
Participants receive brief bedside intervention component. |
|
|
Experimental ALL |
Participants receive brief bedside, peer support, case management+ voucher, and SELF group intervention components. |
|
|
Experimental BB, PS, CM |
Participants receive brief bedside, peer support, and case management+ voucher intervention components. |
|
|
Experimental BB, PS, G |
Participants receive brief bedside, peer support, and SELF group intervention components. |
|
|
Experimental BB, PS |
Participants receive brief bedside and peer support intervention components. |
|
Recruiting Locations
Little Rock, Arkansas 72205
More Details
- Status
- Recruiting
- Sponsor
- University of Arkansas
Detailed Description
Arkansas is a rural southern state with a high toll of homicide relative to its total population (AR ranks 8th nationally in firearm homicide rates). This study will engage community partners throughout Central Arkansas in a multi-level, multi-faceted intervention to reduce the toll of violent assault on individuals and communities. An optimization randomized control trial (ORCT) design will be used to test the preliminary efficacy of a multi-level intervention with an explicit focus on secondary violence prevention through hospital-community partnerships to prevent escalation of firearm violence among survivors living in counties in Central Arkansas, the region of the state where violent assault is greatest. The study will also incorporate key implementation science metrics to evaluate the feasibility and reach of the proposed intervention.