NCT06682403

Brief Summary

This study aims to enhance workplace safety by implementing a firearm safety program at Penn Medicine Pennsylvania Hospital (PAH). The option to store firearms securely during visits is offered to firearm owners. The study focuses on understanding barriers and facilitators to this program and piloting methods to collect data on firearm storage device use. The approach prioritizes participant confidentiality and pragmatism. The study design involves iterative pilot testing of data collection methods and comparison of acceptance and usage rates between cable locks and lock boxes through randomization. The intended outcome is to provide evidence supporting the scalability and effectiveness of the program. The study population includes patients and visitors who accept firearm safety materials or express interest in receiving a firearm storage device. The primary outcome measure is survey response rate, with secondary outcomes including firearm storage behavior and likelihood of using a gun safety device. Additionally, the study explores variations in survey distribution methods.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
49

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2024

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

June 7, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2024

Completed
1 month until next milestone

First Posted

Study publicly available on registry

November 12, 2024

Completed
1.1 years until next milestone

Results Posted

Study results publicly available

December 17, 2025

Completed
Last Updated

December 17, 2025

Status Verified

December 1, 2025

Enrollment Period

4 months

First QC Date

June 7, 2024

Results QC Date

May 7, 2025

Last Update Submit

December 2, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Survey Response Rate

    The primary outcome measure is survey response rate, defined as whether an eligible visitor or patient completed the firearm storage survey after accepting firearm safety materials or after scanning the QR code on the study poster.

    From 2 to 4 weeks

Secondary Outcomes (2)

  • Rate of Full Firearm Storage at Follow-Up

    From 2 to 4 weeks

  • Likelihood of Using Cable Lock Within the Next Week (Extremely Unlikely to Extremely Likely Scale).

    From 2 to 4 weeks

Study Arms (2)

Individual receives cable lock as default

EXPERIMENTAL

Participants in this arm are either automatically assigned due to taking a cable lock at the hospital when offered AND fill out the survey OR are randomized into this group by filling out the study survey linked in study materials.

Behavioral: Received cable lock as default

Individual has a choice between cable lock and lock box

EXPERIMENTAL

Participants in this arm are randomized into it based on NOT taking a cable lock at the hospital when offered AND fill out the survey OR are randomized into this group by filling out the study survey linked in study materials.

Behavioral: Choice between cable lock or lock box

Interventions

Participant will have the option to select a lock box or cable lock shipped to their address after filling out the study survey.

Individual has a choice between cable lock and lock box

Participants will receive a cable lock as the default safety device option after filling out the survey. If the participant took a cable lock during their hospital visit and noted this in the survey, they will not be shipped a cable lock. If participants did not take a cable lock and noted this in the survey, they will be shipped a cable lock.

Individual receives cable lock as default

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Individuals who are visitors or patients at Penn Medicine Facilitates who are identified through security screening as carrying a firearm, and who accept a firearm safety brochure and scan the QR code in the brochure; OR
  • Any patient or visitor interested in receiving a firearm storage device who self-selects into the study by scanning the QR code on the study poster; OR
  • Any individual interested in receiving a firearm storage device who clicks the link to the survey posted on the Penn Medicine Safety Measures website that is included health system appointment reminders.

You may not qualify if:

  • Individuals who have already completed the survey or have already requested a gun safety device.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pennsylvania Hospital

Philadelphia, Pennsylvania, 19107, United States

Location

Related Publications (1)

  • Cunningham RM, Walton MA, Carter PM. The Major Causes of Death in Children and Adolescents in the United States. N Engl J Med. 2018 Dec 20;379(25):2468-2475. doi: 10.1056/NEJMsr1804754. No abstract available.

    PMID: 30575483BACKGROUND

Related Links

Results Point of Contact

Title
Dr. Mucio Kit Delgado
Organization
University of Pennsylvania

Study Officials

  • Mucio K Delgado, MD

    University of Pennsylvania

    PRINCIPAL INVESTIGATOR
  • Elinore Kaufman, MD

    University of Pennsylvania

    PRINCIPAL INVESTIGATOR
  • Katelin Hoskins, MD

    University of Pennsylvania

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants who fill out the survey linked to study posters and brochures will be randomized to either receive a cable lock as the default safety device option or the choice between a cable lock or lock box, shipped to their address. For individuals who take a cable lock at time of receiving a brochure, they are automatically assigned into the cable lock group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor of Emergency Medicine and Epidemiology

Study Record Dates

First Submitted

June 7, 2024

First Posted

November 12, 2024

Study Start

June 1, 2024

Primary Completion

October 1, 2024

Study Completion

October 1, 2024

Last Updated

December 17, 2025

Results First Posted

December 17, 2025

Record last verified: 2025-12

Locations