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Adult Trauma Centers RE-AIM at Gun Safety

ACTFAST: Urban and Rural Trauma Centers RE-AIM at Firearm Injury Prevention

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06302452
Acronym
ACTFAST
Enrollment
1776
Registered
2024-03-08
Start date
2024-10-30
Completion date
2028-04-30
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Firearm Injury, Safety Issues

Brief summary

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.

Interventions

Firearm access screening, brief firearm safe storage intervention, and referral to community and preventive health resources

Sponsors

Johns Hopkins University
Lead SponsorOTHER
National Institute on Minority Health and Health Disparities (NIMHD)
CollaboratorNIH
Rhode Island Hospital
CollaboratorOTHER
WellSpan Health
CollaboratorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

The trial uses a unidirectional crossover stepped wedge design with a sequential roll-out of the intervention, ACTFAST, RE-AIM implementation framework, over several discrete time points or "steps." Each of the three trauma centers will be randomly assigned to one step that will determine when they crossover from control to implementation. Data are collected over multiple wedges, each 4-6 months in length. During the first wedge, none of the participating trauma centers will receive ACTFAST. During the second wedge, the first trauma center completes the Adoption and Implementation period. Over the third wedge, the first center shifts to the Maintenance period, the second trauma center enters the Adoption and Implementation period, and the remaining cohort stays in the control condition. This pattern continues until all trauma centers have progressed from control condition through the active implementation period.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Electronic Medical Record (EMR) Participants: Inclusion Criteria: * trauma patients admitted to adult trauma inpatient services at participating institutions

Exclusion criteria

* none Patient participants Inclusion Criteria: * 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.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of admitted injured patients receiving each element of the ACTFAST Program48 weeksACTFAST 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 dischargeAmong 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 weeksThis outcome will be measured using the patient survey data adapted from prior work by the study team.

Secondary

MeasureTime frameDescription
Clinician firearm safety knowledge and confidence as assessed by survey48 weeksThis outcome will be measured using clinician survey data derived from multiple sources developed through the prior work of members of the study team.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKatherine Hoops, MD, MPH

Johns Hopkins University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026