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University of Michigan Youth Violence Prevention Emergency Department Brief Intervention (Project Sync)

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University of Michigan

Status

Completed

Conditions

Violence

Treatments

Behavioral: Project Sync

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT02586766
5U01CE001957-05

Details and patient eligibility

About

The purpose of this study is to determine whether a brief motivational interviewing intervention given during emergency department care to 14-20 year olds seeking treatment, could reduce youth violence.

Full description

This Emergency Department (ED) based study will test the effectiveness of a tailored therapist delivered motivational interviewing intervention, and an informational pamphlet control condition (IC) on reducing violence in 14-20 year olds who present to the Hurley Medical Center (HMC). Eligible adolescents at the Hurley Medical Center (HMC) emergency department (ED) (based on eligibility criteria) will complete a computerized online survey. The goal of the intervention was to examine ways to reduce and prevention youth violence using techniques to change behavior in a respectful, non-confrontational, and non-judgmental manner. This one-on one counseling approach emphasizes individual choice and responsibility and differentiates between future goals/values and current behavior. At 2-months following their ED visit, eligible adolescents (both from the intervention group and control group) will meet with a research assistant and self-administer an online computerized follow-up survey. An online survey tool will be used for baseline, follow up and post-test surveys. Participants will self-administer the survey at the time of follow up, post-test and baseline.

Enrollment

409 patients

Sex

All

Ages

14 to 20 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. adolescents (ages 14-20) presenting to the Hurley Medical Center for a medical injury or illness (except exclusions noted below);
  2. adolescents will the ability to provide informed assent/consent depending on age;
  3. access to a parent or guardian in person or by telephone for parental consent for adolescents ages 14-17 (over 90% of adolescents had a parent/guardian present based on our prior work);
  4. currently residing in the intervention or control area;

Exclusion criteria

  1. adolescents who do not understand English;
  2. prisoners;
  3. adolescents with abnormal vital signs;
  4. adolescents deemed unable to provide informed consent by Emergency Department or research staff (e.g., intoxication, mental incompetence);
  5. adolescents treated in the Emergency Department for suicide attempts or sexual assault (because they present in high psychological distress requiring intensive attention and intervention by Emergency Department staff).

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

409 participants in 2 patient groups

Behavioral: Project Sync
Experimental group
Description:
Brief 30 minute on-on-one private motivation interviewing intervention during emergency department care
Treatment:
Behavioral: Project Sync
Comparison Group
No Intervention group
Description:
This group did not receive an intervention, but did receive an informational pamphlet of resources in the area (enhanced usual care).

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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