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NCT02257944 Clinical Trial

Assessing and Reducing Risk of Violent Re-Injury Among Victims of Urban Violence

Violence Clinical Trial

— VOV-RCT  

Official title:
Assessing and Reducing Risk of Violent Re-Injury Among Victims of Urban Violence: A Randomized Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT02257944
Other study ID # LSUHSC-8692
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 2, 2014
Last updated October 6, 2014
Start date October 2014
Est. completion date January 2016

Study information
Verified date October 2014
Source Conrad, Erich J., M.D.
Contact Erich J Conrad, MD
Phone 504-903-3417
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of the study is to develop a program to help people to lower their chances of being violently injured again.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 100
Est. completion date January 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- age between 18-65 years

- intentionally injured in community violence.

- admitted to a Level 1 trauma center

- able to provide voluntary informed consent

Exclusion Criteria:

- under the age of 18 or over the age of 55.

- not fluent in the English language

- patients with suspected mental retardation or active psychosis as determined by brief clinical screen.

- patients currently in legal detention status

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Motivational Interviewing
Brief hospital-based intervention, rooted in motivational interviewing
Other:
• Treatment as Usual
treatment as usual

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Conrad, Erich J., M.D.

Outcome
Type Measure Description Time frame Safety issue
Primary Risk Factors for Violence interview of risk factors 3 months No
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