Skip to main content
Clinical Trials/NCT06108141
NCT06108141Active, not recruitingNot Applicable

Implementation of a Novel Virtual Reality Intervention to Support Clinicians' Firearm Safety Counseling Behaviors

Children's Hospital Medical Center, Cincinnati1 site in 1 country130 target enrollmentStarted: December 19, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
130
Locations
1
Primary Endpoint
Percent Change From Baseline in the Percentage of Participants with documentation within the medical record of access to firearms.

Study Overview

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.

Detailed Description

The American Academy of Pediatrics urges pediatricians to counsel parents on the dangers of childhood access to firearms and restrict access through safe storage practices. However, evidence suggests that most pediatricians do not provide firearm-related counseling in real-world clinical practice. This is notable as firearm-related injury is now the leading cause of death in children aged 1-19 years in the United States. Virtual reality (VR) is a type of simulation-based medical education that allows users to interact with virtual environments and characters in a seemingly realistic way. Investigators developed Resident Education And Counseling on Household (REACH) Firearm Safety, a VR curriculum to allow pediatricians to practice screening and counseling on firearm safety. The objective of this proposal is to assess the efficacy of REACH Firearm Safety, along with key implementation metrics, to justify and inform scale and distribution of the training approach. To achieve the objective, Investigators will: (1) Conduct a multi-site two-arm randomized controlled pilot study assessing the efficacy of REACH Firearm Safety and (2) Measure acceptability, appropriateness, fidelity, feasibility, and cost of implementation of REACH Firearm Safety. The proposed research is significant and innovative because it is the first rigorous effort to evaluate the efficacy of VR as a training platform to teach communication skills related to firearm safety counseling.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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

Exclusion Criteria

  • •Resident unable to read or speak English
  • •Resident with continuity clinic outside of inclusion criteria clinics

Arms & Interventions

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.

Intervention: Resident Education And Counseling on Household Firearm Safety (Behavioral)

Modified AAP Safer

Active Comparator

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

Intervention: Modified American Academy of Pediatrics Safer (Behavioral)

Outcomes

Primary Outcomes

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

Time Frame: 6 months

Documentation of discussion during clinical encounter of access to firearms.

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

Time Frame: 6 months

Documentation of discussion during clinical encounter of firearm injury prevention.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

F. Joseph Real

Associate Professor

Children's Hospital Medical Center, Cincinnati

Study Sites (1)

Loading locations...

Similar Trials