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Completed

NCT Number: NCT05436457

Clinical Screening for Firearm Violence Risk

The purpose of the proposed work is to harness cutting-edge machine learning methods to optimize prediction of future firearm violence in youth ages 18-24 so that prevention resources can be allocated efficiently.

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Key information

Conditions

Age range

18 year–24 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hurley Medical Center, Flint, Michigan, United States

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About this study

Firearm violence is a public health crisis in the United States, and new epidemiological data suggest we may have reached a new endemic level of firearm mortality in recent years. Youth are disproportionately affected by firearm violence, with those age 18-24 being demonstrably the highest risk group. This study will recruit 1,500 youth age 18-24 from urban emergency departments (EDs) in three broadly different locales-Flint, Philadelphia, and Seattle-and administer a baseline survey covering several domains of potential risk factors for future violence, and follow up with those youth at 6- and 12-months to ascertain the primary outcome-firearm violence involvement (as victim or perpetrator, including threats and sub-clinical injuries)-as well as the secondary outcomes: high-risk firearm behaviors, non-firearm violence, and violent injury. This work will generate new insights into the prediction of firearm violence, and will lay the ground for future research involving the development and testing of interventions for interpersonal firearm violence both by identifying potential high-leverage modifiable predictive factors, and by focusing on youth most in need of intervention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Flint, Philadelphia, or Seattle Youth between the ages of 18-24 seeking care for any reason at Hurley Medical Center, the Hospital of University of Pennsylvania, Penn Presbyterian Medical Center, or Harborview Medical Center Emergency Department
  • Can provide consent for the study

Exclusion criteria

  • Do not understand English (<1% in prior work)
  • Unable to provide consent due to mental status (e.g., alcohol intoxication, acute psychosis) or medical instability.
  • ED visit requiring intensive psychosocial services (e.g., sexual assault, psychosis, active suicidal ideation, or child abuse)
  • In active police custody/prisoners (as they cannot provide consent)

Treatment and study plan

Primary outcomes

  1. Firearm Violence Involvement

    Time frame: 1 Year After Baseline ED Visit

    The primary outcome for this study is firearm violence involvement, as perpetrator or victim. This will be measured in part by the Conflict Tactics Scale 2, as established by Straus et al. CTS-2 is comprised of a 6-point scale, measuring how often the respondent has experienced each type of violence, ranging from never to more than 20 times. The primary outcome here will be a binary indicator comprised of any affirmative response to the questions asked as part of items 1-3 below, or any firearm events found from the objective chart review.

    • Two self-reported measurements of firearm violence perpetration adapted from the modified conflict tactics scale (CTS-2).
    • Two self-reported measurements of firearm violence victimization adapted from the modified conflict tactics scale (CTS-2).
    • Presentation to the emergency department for a firearm injury (ICD-10 codes: X72-X74, W32-W34, X93-X95), measured based on objective chart review during the one year following baseline.

Secondary outcomes

  1. Risky Firearm Behaviors

    Time frame: 1 Year After Baseline ED Visit

    As established by Carter et al based on a) twelve items from the Tulane Youth Study that measure firearm carriage and discharge in high-risky situations (e.g., discharging a firearm while committing a crime, or carrying a firearm while using drugs); b) the four firearm violence perpetration/victimization outcomes listed under the primary outcome; and c) firearm violence threats (as victim or perpetrator), as measured by the modified conflict tactics scale (CTS-2)

  2. Non-Firearm Violence

    Time frame: 1 Year After Baseline ED Visit

    22 self-reported measurements for non-firearm violence perpetration (11 for partner, 11 for non-partner) adapted from the CTS-2, 22 self-reported measurements for non-firearm violence victimization (11 for partner, 11 for non-partner) adapted from the CTS-2, and 6 items about fighting, adapted from the National Longitudinal Study of Adolescent Health.

  3. Violent Injury

    Time frame: 1 Year After Baseline ED Visit

    Presentation to the emergency department for any violent injury, measured based on objective chart review during the one year following baseline.

Sponsors and collaborators

Lead sponsor

University of Michigan

Other

Collaborators

  • Centers for Disease Control and Prevention

Registry information

Official study title

Multi-site External Validation and Improvement of a Clinical Screening Tool for Future Firearm Violence

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Jun 29, 2022
Registry last updated
Aug 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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