- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02642224
Trauma Services Intervention to Prevent Violence (TSI)
June 28, 2018 updated by: Steven M. Albert, University of Pittsburgh
Primary outcome: Research participants and their network contacts will be followed over 6 months to assess whether a social work case management protocol results in reduction of trauma services recidivism and criminal violence arrests.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Allegheny County, PA continues to suffer between 100-120 homicides each year, with perhaps 2-3 times as many gunshot injuries that require hospitalization.
Firearm homicides overwhelmingly affect African American men aged 15-35.
Building on prior efforts in violence prevention, the investigators propose to launch a hospital trauma service intervention that will take advantage of a "teachable moment" in the emergency room.
All four hospitals providing Level I Trauma services in Allegheny County have agreed to host the program, an evidence-based effort developed by the National Network of Hospital Violence Intervention (NNHVI).
Adaptation of the NNHVI model will focus on the social networks of gunshot victims as well as the victims themselves.
Intervention efforts will range from job training and mentoring to relocation to different communities.
The investigators will offer the opportunity to participate in the research and receive the intervention to all gunshot victims identified in county Level I trauma services.
Participants in the research protocol will be asked to recruit their high-risk social network members for the intervention.
Study Type
Interventional
Enrollment (Actual)
111
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15261
- University of Pittsburgh, Graduate School of Public Health
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age 18+
- Gunshot victim treated and discharged from Level I trauma facility; or member of social network of gunshot victim who may be high risk of firearm violence -
Exclusion Criteria:
- Gunshot wound because of suicide attempt
- Gunshot wound because of non-violent episode (e.g., hunting accident)
- Unable to participate in research interview because of cognitive deficit
- Planning to leave community as result of shooting
- Discharged from trauma service to prison
- Unable to provide informed consent -
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Social work intervention
The National Network of Hospital Violence Intervention (NNHVI) suggests that intervening when gunshot victims are receiving treatment in hospital trauma services may be effective in linking high-risk individuals to appropriate case management services, and that this service linkage may lower the risk of further violence.
Our adaptation of the NNHVI model will focus on the social networks of gunshot victims as well as the victims themselves.
Intervention efforts will range from job training and mentoring to relocation to different communities.
|
The National Network of Hospital Violence Intervention (NNHVI) suggests that intervening when gunshot victims are receiving treatment in hospital trauma services may be effective in linking high-risk individuals to appropriate case management services, and that this service linkage may lower the risk of further violence.
Our adaptation of the NNHVI model will focus on the social networks of gunshot victims as well as the victims themselves.
Intervention efforts will range from job training and mentoring to relocation to different communities.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Trauma services recidivism
Time Frame: 6 months
|
Readmission to hospital trauma service because of firearm injury
|
6 months
|
Arrest for violent crime
Time Frame: 6 months
|
Arrests involving criminal violence noted in DA docket
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Social work case management goals
Time Frame: 6 months
|
Educational program enrollment, job training, receipt of drug and alcohol treatment, trauma counseling
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2014
Primary Completion (Actual)
May 1, 2018
Study Completion (Actual)
May 1, 2018
Study Registration Dates
First Submitted
December 27, 2013
First Submitted That Met QC Criteria
December 29, 2015
First Posted (Estimate)
December 30, 2015
Study Record Updates
Last Update Posted (Actual)
July 2, 2018
Last Update Submitted That Met QC Criteria
June 28, 2018
Last Verified
June 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UN2013-67786
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Data will be archived and made available to qualified investigators
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Skin Injury Due to Violence
-
Pusan National University HospitalCompletedDermatologic Disorders | Injury Due to LaserKorea, Republic of
-
Orthocare Innovations, LLCNational Institute on Disability, Independent Living, and Rehabilitation...RecruitingStroke | Upper Limb Amputation | Upper Limb Weakness Due to Central Neurologic Injury | Upper Limb Weakness Due to Peripheral Neurologic Injury | Upper Limb Weakness Due to Nerve Reconstruction | Upper Limb Weakness Due to Tendon Transfer SurgeryUnited States
-
Johann Wolfgang Goethe University HospitalKlinikum LudwigshafenCompletedComplications Due to Coronary Artery Bypass Graft | Injury of Internal Mammary ArteryGermany
-
Chang Gung Memorial HospitalCompletedVirus Diseases | Disorder Related to Transplantation | Injury Due to Exposure to External Cause
-
Pain ConcernThe Thistle Foundation; Health and Social Care Alliance Scotland (the ALLIANCE) and other collaboratorsCompletedChronic Pain | Chronic Pain Syndrome | Chronic Pain, Widespread | Chronic Pain Due to Trauma | Chronic Pain Due to Malignancy (Finding) | Chronic Pain Due to Injury | Chronic Pain Post-Procedural | Chronic Pain HipUnited Kingdom
-
University of ArizonaNational Cancer Institute (NCI)RecruitingOther Skin Changes Due to Chronic Exposure to Nonionizing RadiationUnited States
-
Prehospital Center, Region ZealandNot yet recruitingDrowning | Drowning, Near | Submersion | Submersion - Accidental | Submersion or Drowning Due to Being Washed Overboard | Submersion or Drowning Due to Being Thrown Overboard | Submersion or Drowning Due to Ship Sinking, Water Skier Injured | Submersion or Drowning Due to Boat Submerging, Swimmer... and other conditionsDenmark
-
Neuromed IRCCSCompletedToxicity Due to RadiotherapyItaly
-
University of Sao PauloFundação de Amparo à Pesquisa do Estado de São PauloCompletedPoor Metabolizer Due to Cytochrome P450 CYP2C9 Variant | Poor Metabolizer Due to Cytochrome p450 CYP2C19 VariantBrazil
-
DeviceFarm, Inc.Symbio, LLC; Center for Dermatology Clinical Research, Inc.CompletedOnychomycosis Due to Trichophyton Rubrum | Onychomycosis Due to Trichophyton MentagrophytesUnited States
Clinical Trials on Social Work Case Management
-
The Hong Kong Polytechnic UniversityCompleted
-
Genossenschaft Gesundheitsprojekt Mannheim e.GMerck Sharp & Dohme LLC; Heidelberg University; pfm medical Institute gGmbH,...Unknown
-
The Hong Kong Polytechnic UniversityRecruiting
-
Brown UniversityThe Miriam HospitalCompletedOptimizing PrEP Uptake & Adherence Among Male Sex Workers (MSW) Using a 2-stage Randomization DesignPreventionUnited States
-
Brown UniversityUniversity of California, Los Angeles; National Institute of Nursing Research... and other collaboratorsRecruiting
-
Children's Hospital of PhiladelphiaUniversity of Pennsylvania; Eagles Autism Challenge, IncCompleted
-
Alaine E Hernandez, PhDAmerican Music Therapy AssociationRecruitingDementia | Telemedicine | Aging WellUnited States
-
Medical College of WisconsinNational Institute of Nursing Research (NINR)Recruiting
-
National Taiwan University HospitalCompleted
-
Medical College of WisconsinCompleted