NCT06108141

Brief Summary

The goal of this clinical trial is to assess the efficacy of REACH Firearm Safety in a sample of pediatric residents. The main question it aims to answer are: Do residents who have completed REACH Firearm Safety have increased documentation in the electronic medical records for screening and counseling for safe firearm storage? Participants will be asked to engage in a virtual reality curriculum (REACH Firearm Safety). Researchers will compare the REACH Firearm safety group to a group of participants who complete an abbreviated online training.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
130

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2023

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 23, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

October 30, 2023

Completed
2 months until next milestone

Study Start

First participant enrolled

December 19, 2023

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

June 27, 2024

Status Verified

June 1, 2024

Enrollment Period

1 year

First QC Date

October 23, 2023

Last Update Submit

June 25, 2024

Conditions

Keywords

Virtual RealitySimulation Based Medical EducationFirearm Injury

Outcome Measures

Primary Outcomes (2)

  • Percent Change From Baseline in the Percentage of Participants with documentation within the medical record of access to firearms.

    Documentation of discussion during clinical encounter of access to firearms.

    6 months

  • Percent Change From Baseline in the Percentage of Participants with documentation within the medical record of counseling on firearm injury prevention.

    Documentation of discussion during clinical encounter of firearm injury prevention.

    6 months

Study Arms (2)

Resident Education And Counseling on Household (REACH) Firearm Safety

EXPERIMENTAL

Resident participants will complete a modified online self-guided American Academy of Pediatrics (AAP) Safer curriculum. Next, residents will complete REACH individually with a trained facilitator.

Behavioral: Resident Education And Counseling on Household Firearm Safety

Modified AAP Safer

ACTIVE COMPARATOR

Resident participants will complete a modified online self-guided American Academy of Pediatrics (AAP) Safer curriculum.

Behavioral: Modified American Academy of Pediatrics Safer

Interventions

An intervention that includes a self-directed online curriculum and virtual reality simulations, designed to teach firearm screening and counseling among clinicians.

Also known as: REACH Firearm Safety
Resident Education And Counseling on Household (REACH) Firearm Safety

An intervention that includes a self-directed online curriculum.

Also known as: Modified AAP Safer
Modified AAP Safer

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Resident with continuity clinic at either Kentucky Clinic South, University of Kentucky (UK) Internal Medicine and Pediatrics group, CCHMC Hopple Street Neighborhood Health Center, or University of Cincinnati (UC) Hoxworth Medicine-Pediatrics Clinic

You may not qualify if:

  • Resident unable to read or speak English

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, 45229, United States

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

October 23, 2023

First Posted

October 30, 2023

Study Start

December 19, 2023

Primary Completion

December 31, 2024

Study Completion

December 31, 2024

Last Updated

June 27, 2024

Record last verified: 2024-06

Data Sharing

IPD Sharing
Will not share

Locations