CClinicalTrials.gg
RecruitingNCT06719713Updated May 14, 2026

Store Safely: Rural Firearm Injury Prevention for Families

An interventional study of Store Safely in Firearm Injury, sponsored by University of Michigan. Recruiting at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-14.

Sponsored by University of Michigan · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started Aug 2025; still recruiting 1 year 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
600
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The researchers are testing a firearm safety prevention strategy tailored for families with children who reside in a rural area. Researchers hypothesize that the intervention will lead to improvements in household firearm storage.

02

Conditions studied

  • Firearm Injury

Keywords

  • rural
  • firearm safe storage
  • injury prevention
  • suicide prevention
  • community education
03

In context

Suicide Prevention

190 studies on the registry are indexed under Suicide Prevention; 87 are open to participants now.

This study's planned enrollment of 600 is above the median of 150 across 169 interventional studies indexed under Suicide Prevention.

Browse Suicide Prevention studies →

Lead sponsor

University of Michigan is the lead sponsor of 1,475 studies on the registry; 196 are open to participants now.

Of its 162 completed or terminated interventional studies of FDA-regulated products, 128 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Provision of signed and dated informed consent form
  • Age 18 or older
  • English-speaking
  • Have a child under 18 living at home
  • Currently keep at least one firearm on their property
  • Reside in Michigan's Upper Peninsula (U.P.)
  • Access to a computer/mobile device and wifi
  • Have sufficient information about household storage to complete surveys

Exclusion criteria

Exclusion Criteria:

  • Unable to be consented in English
  • Under the age of 18
  • Lack of firearm on their property
  • No child in the home
  • Residence outside the U.P.
  • No access to technology
  • Previously enrolled in 2020 pilot project
  • Previously access the Store Safely website
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
600 participants (estimated)

Study arms

  • Experimental
    Store Safely

    The Store Safely arm (consisting of a community sample) will receive the Store Safely intervention, usual community-based care, and 988 suicide and crisis lifeline number and a publicly available safe storage information resource numbers.

    Behavioral: Store Safely

  • No intervention
    Waitlist control

    The waitlist control group (consisting of a community sample) will not receive the intervention during the clinical trial but will be offered 988 suicide and crisis lifeline number and a publicly available safe storage information resource numbers. Following the clinical trial they will have access to the Store Safely intervention.

Interventions

  • BehavioralStore Safely

    The Store Safely intervention occurs online and is self-administered. Once directed to the Store Safely website, participants are welcomed and instructed to complete each step of the online program. Upon clicking "Start," participants are taken to Step 1 of the intervention and instructed to review a brief video. Step 2 involves a review of a data infographics. Participants are then directed to the Decision Aid in Step 3. In Step 4, participants are instructed to complete the Family Firearm Storage Action Plan. In Step 5, participants will review another brief video. There will also be an optional step, consisting of a resource page that details local options for obtaining safe storage devices. At the end of each step, participants mark a checkbox to indicate they have completed the intervention activity which facilitates website analytics of participant engagement. Lastly, participants are thanked and provided with details about the final steps of the trial.

06

What researchers measure

Primary outcomes

  1. Number of firearms stored locked

    Measured using a self-report item from the Family Firearm Storage Behaviors Survey (Ewell Foster et al., 2024) administered at 3 months. May range from 1-40 based on pilot data

    Time frame: Approximately 3 months

  2. Parent Engagement in Harm Reduction Firearm Storage Behaviors Score

    Measured using the Family Firearm Storage Behaviors Survey (Ewell Foster et al., 2024) administered at 3 months. The survey is 14 items, endorsed as Y/N. Score range is 0-14.

    Time frame: Approximately 3 months

Secondary outcomes

  1. Parent Self-Efficacy for Firearm Safety Questionnaire

    Time frame: Baseline, Immediate/2-Week

  2. Number of firearms unloaded

    Measured using a self-report item from the Family Firearm Storage Behaviors Survey (Ewell Foster et al., 2024) administered at 3 months.

    Time frame: Approximately 3 months

  3. Number of firearms unlocked and loaded

    Measured using a self-report item from the Family Firearm Storage Behaviors Survey (Ewell Foster et al., 2024) administered at 3 months.

    Time frame: Approximately 3 months

07

Study locations

1 of 2 sites recruiting
  • University of Michigan
    Ann Arbor, Michigan 48109, United States
    • Christina Magness · Contact · cmagness@med.umich.edu · 734-252-6315
    • Cynthia Ewell Foster, Ph.D. · Principal investigator
    Not yet recruiting
  • Marquette County Health Department
    Negaunee, Michigan 49866, United States
    • Sarah Derwin · Contact · sderwin@mqtco.gov · 906-475-9977
    • Cynthia Ewell Foster · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — After the study is complete and data has been cleaned and de-identified, the archived data will be transmitted to and securely stored at the University of Michigan Institute for Firearm Injury Prevention Data Repository, for use by other researchers including those outside of the study.

Supporting information: Study protocol, Icf

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06719713
Lead sponsor
University of Michigan
Collaborators
Centers for Disease Control and Prevention, Marquette County Health Department
Responsible party
Cynthia Ewell Foster (Clinical Associate Professor of Psychiatry, University of Michigan) — Principal investigator
First posted
Dec 6, 2024
Start date
Aug 11, 2025
Primary completion
May 2027 (estimated)
Completion
May 2027 (estimated)
Last update
May 14, 2026

Study contacts

Christina Magness
Contact
cmagness@med.umich.edu
734-252-6315
Lauren Majlinger, BA
Contact
lmajling@med.umich.edu
7349312162
Cynthia Ewell Foster, Ph.D.
principal investigator · University of Michigan

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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