Adult Trauma Centers RE-AIM at Gun Safety

Part of paid clinical trials in Baltimore, Maryland.

Sponsor
Johns Hopkins University
Study ID
NCT06302452
Status
Enrolling By Invitation

Conditions

  • Firearm Injury
  • Safety Issues

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Adopting Comprehensive Training for FireArm Safety in Trauma Centers — BEHAVIORAL
    Firearm access screening, brief firearm safe storage intervention, and referral to community and preventive health resources

Study Details

The goal of this interventional study is to evaluate the implementation and effectiveness of a comprehensive a universal firearm injury prevention program, ACTFAST (Adopting Comprehensive Training for FireArm Safety in Trauma centers), in level 1 trauma centers. The main aims of the study are: 1. (Primary Aim 1) Increase the adoption, implementation, and maintenance of a universal firearm injury prevention intervention at three participating trauma centers in the mid-Atlantic states; 2. (Primary Aim 2) Assess firearm injury prevention knowledge, attitudes, and safe storage practices among trauma patients treated within participating trauma centers.

Key Dates

Start date
Oct 30, 2024
Status verified
Mar 2026
Primary completion
Mar 1, 2028
Completion
Apr 30, 2028

Study Design

Enrollment
1,776 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER

Arms

  • No Intervention: No Intervention: Standard Care
    All trauma patients will receive standard routine care which may include some screening and counseling on gun safety.
  • Experimental: ACTFAST Intervention
    During the implementation and maintenance periods, all trauma patients will receive study activities including firearm access screening, counseling on safe storage practices, and referral to safe storage and other community resources as appropriate.

Primary Outcome Measure

Proportion of admitted injured patients receiving each element of the ACTFAST Program [ Time Frame: 48 weeks ]

Locations (3)

FacilityCityStateZIPSite coordinators
Johns Hopkins Bayview Medical CenterBaltimoreMaryland21287-
Johns Hopkins HospitalBaltimoreMaryland21287-
WellSpan HealthYorkPennsylvania17402-

Find similar trials in Baltimore, MD

By research site
Johns Hopkins Bayview Medical Center· Baltimore, MDJohns Hopkins Hospital· Baltimore, MDWellSpan Health· York, PA

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