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Trial · NCT07886983

Firearm Secure Storage Device Distribution RCT

NCT07886983, Not applicable, Not yet recruiting, University of Pennsylvania

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Firearm Secure Storage Device Distribution RCT. Trials, record NCT07886983. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07886983

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Firearm Secure Storage Device Distribution RCT
NCT number
NCT07886983
Status
Not yet recruiting
Phases
Not applicable
Enrollment
1,858 participants, estimated
Lead sponsor
University of Pennsylvania
Conditions
Firearm Safety, Firearm Safety Storage
Interventions
Cable locks, Lock box, Lock box and cable locks
First posted
2026-10-21
Last updated
2026-11-12

Source ClinicalTrials.gov

Registered outcomes27

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryProportion of Participants Reporting All Firearms Stored Securely at 30 Days30 days after enrollment
Proportion of participants reporting that all firearms in or around their home are stored securely (vs. some or none) on the 30-day follow-up survey. Secure storage will be assessed through participant self-report using the following response options: Yes, all of them (1); Yes, some of them (2); None of them (3); Not sure (4); No guns in or around home (5); and Prefer not to answer (6).
SecondaryProportion of participants with all firearms stored securely at 3 months3 months after enrollmentProportion of participants reporting that all firearms in the household are stored securely (vs. some or none) on the 3-month follow-up survey.
SecondaryProportion of participants changing from no firearms stored securely to some or all firearms stored securely at 1 month30 days after enrollmentParticipants reporting that some household firearms are stored securely (vs. none) on 1 month follow-up survey after device distribution.
SecondaryProportion of participants changing from no firearms stored securely to some or all firearms stored securely at 3 months3 months after enrollmentParticipants reporting that some household firearms are stored securely (vs. none) on 3 month follow-up survey after device distribution.
SecondaryNumber of preferred firearm storage devices requestedBaseline (enrollment)Among patients randomized to the preferred device arm, the number of firearm storage devices requested by participants will be assessed.
SecondaryIncremental intervention cost per participantBaseline (enrollment)Incremental cost of delivering the intervention, including the cost of firearm storage devices and associated shipping costs. Costs will be calculated in US dollar per participant
OtherNumber of Participants by Cable Lock Frequency at 30 Days30 days after enrollment
Frequency of cable lock use among participants reporting use of cable locks on firearms at the 30-day follow-up assessment. Participants will report how often cable locks are used using the following response options: * Always (1) * More than half the time (2) * Less than half the time (3)
OtherNumber of Participants by Cable Lock Frequency at 90 Days90 days after enrollment
Frequency of cable lock use among participants reporting use of cable locks on firearms at the 90-day follow-up assessment. Participants will report how often cable locks are used using the following response options: * Always (1) * More than half the time (2) * Less than half the time (3)
OtherNumber of Participants by Cable Lock Frequency at 180 Days180 days after enrollment
Frequency of cable lock use among participants reporting use of cable locks on firearms at the 180-day follow-up assessment. Participants will report how often cable locks are used using the following response options: * Always (1) * More than half the time (2) * Less than half the time (3)
OtherNumber of Cable Locks by Recipient Type at 30 Days30 days after enrollment
Number of cable locks reported as being held by the participant (self), family members, friends, or other individuals at the 30-day follow-up assessment. Participants will report the number of cable locks held by each recipient type.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07886983

GET https://conductscience.org/api/trials/v1/NCT07886983/registered?page=2