跳至主要内容
临床试验/NCT06302452
NCT06302452Enrolling By Invitation不适用

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

Johns Hopkins University3 个研究点 分布在 1 个国家目标入组 1,776 人开始时间: 2024年10月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
1,776
试验地点
3
主要终点
Percentage of admitted injured patients receiving elements of the ACTFAST Program

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • 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.
  • 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:

研究组 & 干预措施

No Intervention: Standard Care

No Intervention

All trauma patients will receive standard routine care which may include some screening and counseling on gun safety.

ACTFAST Intervention

Experimental

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.

干预措施: Adopting Comprehensive Training for FireArm Safety in Trauma Centers (Behavioral)

结局指标

主要结局

Percentage of admitted injured patients receiving elements of the ACTFAST Program

时间窗: 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

时间窗: 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

时间窗: 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.

次要结局

  • Clinician firearm safety knowledge and confidence as assessed by survey(48 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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