Adult Trauma Centers RE-AIM at Gun Safety (ACTFAST) Prevention
- Conditions
- Firearm InjurySafety Issues
- Interventions
- Behavioral: Adopting Comprehensive Training for FireArm Safety in Trauma Centers
- Registration Number
- NCT06302452
- Lead Sponsor
- Johns Hopkins University
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 1776
- trauma patients admitted to adult trauma inpatient services at participating institutions
- 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 written consent.
Exclusion Criteria:
- 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).
Staff participants
Inclusion Criteria:
- trauma service physician, physician assistant, nurse practitioner, nurse or social worker at participating pediatric trauma center
Exclusion Criteria:
- none
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description ACTFAST Intervention Adopting Comprehensive Training for FireArm Safety in Trauma Centers 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 Measures
Name Time Method Percentage of admitted injured patients receiving elements of the ACTFAST Program Admission, 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 survey 48 weeks This outcome will be measured using the patient survey data adapted from prior work by the study team.
Proportion of admitted injured patients receiving each element of the ACTFAST Program 48 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.
- Secondary Outcome Measures
Name Time Method Clinician firearm safety knowledge and confidence as assessed by survey 48 weeks This outcome will be measured using clinician survey data derived from multiple sources developed through the prior work of members of the study team.
Trial Locations
- Locations (2)
Johns Hopkins Bayview Medical Center
🇺🇸Baltimore, Maryland, United States
Johns Hopkins Hospital
🇺🇸Baltimore, Maryland, United States