跳至主要内容
临床试验/NCT06886776
NCT06886776Enrolling By Invitation不适用

Implementing A Secure Firearm Storage Program in Illinois Health Centers in Partnership With AllianceChicago and the Illinois Primary Health Care Association (COMMUNITY ASPIRE)

Northwestern University2 个研究点 分布在 1 个国家目标入组 1,086 人开始时间: 2026年7月14日最近更新:
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
1,086
试验地点
2
主要终点
Parent-reported reach of S.A.F.E. Firearm

研究概览

简要总结

This randomized controlled trial will take place in up to 15 community health centers across the state of Illinois. Researchers will be studying S.A.F.E. Firearm, a program that aims to increase secure storage of firearms in homes with children. Specifically, S.A.F.E. Firearm includes a brief conversation between pediatric clinicians and parents/guardians about secure firearm storage and an offer of a free cable firearm lock within the well-child visit. Researchers will also study a package of strategies to help pediatric clinics incorporate this new practice. The strategies include training for clinic personnel and facilitation, or tailored problem-solving support.

The questions the study aims to answer are:

  • How effective is the package of strategies at helping pediatric clinics implement this new practice?
  • How effective is the S.A.F.E. Firearm program at changing parents', caregivers' and guardians' (hereafter, "parents") firearm storage behavior?

Some parents will be invited to complete a brief survey after their visit about their experiences receiving S.A.F.E. Firearm. Some community health center personnel will also be invited to complete an interview about their experiences with S.A.F.E. Firearm and the package of strategies.

详细描述

While some large health systems have successfully implemented secure firearm storage programs such as S.A.F.E. Firearm into routine practice, there is limited research on the implementation of secure firearm storage programs in community settings, such as community health centers, which serve large populations of Americans. These settings often face challenges such as financial pressures and high staff turnover, which were made worse by the COVID-19 pandemic. Therefore, before deploying a secure firearm storage program in this new setting, adaptation is needed. As part of Aim 1 of the grant funding this project, the research team is working with local community-based organizations, firearm safety experts, community health center personnel, and parents, guardians, and caregivers (hereafter, "parents") to understand the changes that need to be made to the S.A.F.E. Firearm program and the package of implementation strategies that have been successfully used in previous studies to help pediatric clinics implement this new practice (training, facilitation). The research team will incorporate needed changes before the present trial will begin.

In the present study, the research team will conduct a hybrid type III effectiveness-implementation trial to test the effect of the adapted S.A.F.E. Firearm program and associated strategies. The trial will be conducted across pediatric well-visits in community health centers across the state of Illinois using a stepped wedge design. Clinics will be randomized into clusters of clinics and the implementation approach (staff training, facilitation) will be activated upon the start of each step.

Aims for the study include:

Aim 2. We will conduct a pragmatic hybrid type III stepped wedge effectiveness-implementation randomized controlled trial with community health centers across Illinois to test the effectiveness of our adapted implementation approach on parent-reported receipt of S.A.F.E. Firearm (i.e., reach; co-primary implementation outcome) and distribution of cable locks by the clinics (co-primary implementation outcome). We will also assess secondary implementation outcomes (stage of implementation, cost, acceptability) and effectiveness outcomes (parent firearm storage behavior).

Aim 3. We will use mixed methods to identify mechanisms.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
None

盲法说明

Data analyst will be blinded to randomization assignment

入排标准

性别
All
接受健康志愿者

入选标准

  • Parent participants
  • Be a parent, caregiver, or legal guardian of a child ages 0-17 who has a well-visit at a participating health care clinic in the state of Illinois
  • Attend the child's well-visit
  • Health care personnel
  • Be employed at a participating health care clinic in the state of Illinois
  • Aged 18+ years

排除标准

  • 未提供

研究组 & 干预措施

Sustainment (training and facilitation removed)

No Intervention

Following the conclusion of the 12 months in which the implementation approaches (training and facilitation) are used at a clinic, outcomes will be assessed for the duration of the study during a "sustainment" window.

No additional training or facilitation will be received during the sustainment period following the experimental period. However, clinics will still continue to deliver S.A.F.E. Firearm.

Control/usual care

No Intervention

During the control data collection phase, no individuals will be exposed to S.A.F.E. Firearm. No training or facilitation will be received. The length of the baseline data collection phase will differ between each "wedge" (i.e., group of clinics) depending on when the group is randomly assigned to cross over into the active implementation phase. All sites will be in the control data collection phase for at least three months before having the interventions activated.

Active implementation phase (training and facilitation received, S.A.F.E. Firearm delivered)

Experimental

Once a group of clinics crosses over from the control data collection phase, the implementation approaches (e.g., training, facilitation) and the S.A.F.E. Firearm program will be enacted. S.A.F.E. Firearm involves pediatric clinicians having a secure firearm storage discussion with a parent during their child's well-visit and offering them a free cable firearm lock. This active implementation phase will last for 12 months.

干预措施: Implementation package (training and facilitation) (Behavioral)

结局指标

主要结局

Parent-reported reach of S.A.F.E. Firearm

时间窗: Reach will be collected via survey sent to parents after well-visits for the 3-year study period (baseline through sustainment phases)

The proportion of eligible pediatric well-visits for which parents report receiving the two components of S.A.F.E. Firearm (discussion of secure firearm storage, offer of a free cable firearm lock)

Reach

时间窗: 2.5 years (duration of the study - control through sustainment)

The proportion of eligible parents who report receiving both S.A.F.E. Firearm intervention components (counseling and lock). The two questions comprising reach ask the parent to report whether the following occurred during their child's recent visit: a member of the health center staff (1) spoke to them about firearm storage and (2) offered them a free firearm lock(s), even if they didn't take one. Response options to each of these questions include: yes, no, don't remember, and prefer not to answer.

Locks distributed

时间窗: 2.5 years (duration of the study - control through sustainment)

The distribution of locks taken during the control phase, active implementation phase, and sustainment phase. Locks for distribution during the active implementation and sustainment phases will be ordered through the study team only. The study team will reach out to each clinic approximately 1 week prior to start of active implementation to ask how many locks were distributed during the control period. The study team will then track how many locks are ordered from each clinic and obtain an estimate from clinics 1 week prior to the end of active implementation of how many locks were distributed during the active implementation phase, and do the same for sustainment.

次要结局

  • Firearm storage behavior(2.5 years (duration of the study - control through sustainment))
  • Acceptability(2.5 years (duration of the study - control through sustainment))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rinad Beidas

Ralph Seal Paffenbarger Professor and Chair, Department of Medical Social Sciences

Northwestern University

研究点 (2)

Loading locations...

相似试验