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NCT06302452

Adult Trauma Centers RE-AIM at Gun Safety

Enrolling by Invitation
NAAges 18+Interventional
Johns Hopkins University
~1,776 participants
Updated 2026-03-09 on ClinicalTrials.gov
What's tested:Adopting Comprehensive Training for FireArm Safety in Trauma Centers

At a glance

Recruiting sites
0 of 3 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Proportion of admitted injured patients receiving each element of the ACTFAST Program
Measured over 48 weeks
+2 more outcomes measured

Conditions

Firearm Injury
Safety Issues

Where it's being run

3 sites across 2 states
Maryland2
Pennsylvania1

Study leadership

  • Katherine Hoops, MD, MPH · PRINCIPAL_INVESTIGATOR · Johns Hopkins University

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

trauma patients admitted to adult trauma inpatient services at participating institutions
at least 18 years of age;
admitted to a participating trauma service for an injury;
fluent in English or Spanish;
able to provide informed consent.
trauma service physician, physician assistant, nurse practitioner, nurse or social worker at participating pediatric trauma center

Exclusion

none
prisoner or in police custody;
admitted due to suicide attempt
any acute conditions that would preclude provision of informed consent or assent (i.e., acute psychosis, altered mental status, cognitive impairment).
none

What this trial measures

  • Proportion of admitted injured patients receiving each element of the ACTFAST Program48 weeks

    ACTFAST components will be collected through retrospective data abstraction of each site's electronic medical record to determine if admitted injured patients received the Screening, Brief Intervention and Referral to Treatment (SBIRT) program components during the different phases of the study.

  • Percentage of admitted injured patients receiving elements of the ACTFAST ProgramAdmission, 2 weeks post discharge

    Among those eligible, compared to pre-implementation, there will be a difference in patients receiving each element of the ACTFAST program as measured by participant survey responses gathered during the participant's admission and 2-weeks post-discharge from survey data derived from multiple sources developed through the prior work of members of the study team.

  • Patient firearm safety attitudes and behaviors as assessed by survey48 weeks

    This outcome will be measured using the patient survey data adapted from prior work by the study team.