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Clinical Trials/NCT07265141
NCT07265141
Not yet recruiting
Not Applicable

An Automated Virtual Reality Intervention to Enhance Firearm Safety Counseling in Pediatrics

Children's Hospital Medical Center, Cincinnati1 site in 1 country30 target enrollmentStarted: January 15, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
30
Locations
1
Primary Endpoint
Acceptability of Intervention Measure

Overview

Brief Summary

Clinicians will complete a screen-based automated virtual reality training intervention to learn how to counsel caregivers of pediatric patients on secure firearm storage.

Detailed Description

The investigators will recruit pediatric clinicians to participate in an automated screen-based virtual reality intervention. Clinicians will be recruited from clinical locations that offer a variety of setting types (urban, suburban, and rural).

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • \- Pediatric Clinicians must meet one of the following inclusion criteria at each study site: Physicians (attending, fellow or resident), Licensed Nurse Practitioner, Physician's Assistant

Exclusion Criteria

  • Unable to read and write in English

Outcomes

Primary Outcomes

Acceptability of Intervention Measure

Time Frame: From completion of the virtual reality intervention to 2 months

Four items, Scale score is average across individual items, Minimum score: 1, Maximum score: 5. higher scores indicate better acceptability

Appropriateness of the Intervention Measure

Time Frame: From completion of the virtual reality intervention to 2 months

Four items, Scale score is average across individual items, Minimum score: 1, Maximum score: 5. higher scores indicate better appropriateness

Feasibility of the Intervention Measure

Time Frame: From completion of the virtual reality intervention to 2 months

Four items, Scale score is average across individual items, Minimum score: 1, Maximum score: 5. higher scores indicate better feasibility

Secondary Outcomes

  • De Novo Survey Item for Assessing Social Cognitive Theory Construct Behavioral Capability(From completion of the virtual reality intervention to 2 months)
  • De Novo Survey Items for Assessing Social Cognitive Theory Construct Self-Efficacy(From completion of the virtual reality intervention to 2 months)
  • De Novo Survey Items for Assessing Social Cognitive Theory Construct Expectations(From completion of the virtual reality intervention to 2 months)
  • De Novo Survey Items for Assessing Social Cognitive Theory Construct Expectancies(From completion of the virtual reality intervention to 2 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

F. Joseph Real

Associate Professor of Pediatrics

Children's Hospital Medical Center, Cincinnati

Study Sites (1)

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