Actively Recruiting

Age: 8Years +
All Genders
ID07427862

Virtual Reality (VR) Use for Reducing Pain and Anxiety in Children Undergoing Interventional Radiology Procedures

Led by Children's Hospital Los Angeles · Updated on 2026-03-09

500

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of Virtual Reality (VR) to reduce pain and anxiety in children aged 8 and older undergoing interventional radiology procedures. The study aims to compare the effects of VR to standard care, assessing both the children's pain and anxiety levels and their caregivers' satisfaction and perception of distress during the procedure. The trial is observational and sponsored by Children's Hospital Los Angeles. Participants will use VR headsets appropriate for their age group during their interventional radiology procedure. Children aged 8 to 18 may use the Pico 4 headset, those 10 and older can use the Meta Oculus Quest Pro, and those 13 and older may use the Pico G3. The VR device is worn starting five minutes before the procedure, throughout the procedure, and up to two minutes after it ends. The VR experience includes immersive 3-D visual, auditory, and tactile feedback designed to distract and engage the child. Throughout the study, participants complete surveys before and after their procedures. Researchers will measure changes in pain and anxiety from before to one hour after the intervention, caregiver satisfaction with the procedure, and participant distress levels. The VR headsets are sanitized before each use to minimize infection risk. Participation involves a single interventional procedure with VR use and associated assessments, with the study expected to conclude in September 2026.

CONDITIONS

Brief Title

Virtual Reality (VR) for Interventional Radiology (IR) Procedures

Who Can Participate

Age: 8Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children who are at least 8 years old
  • Children who speak English, with caregivers who speak English or Spanish
  • Children scheduled for an interventional radiology procedure
  • Children with typical development as reported by parents, without developmental delays
Not Eligible

You will not qualify if you...

  • Children currently taking pain or anxiety medications
  • Children with psychiatric disorders, organic brain syndrome, intellectual disability, or other cognitive/neurological disorders
  • Children with visual, hearing, or tactile impairments affecting study tasks
  • Children with a history of seizure disorder
  • Children currently experiencing flu-like symptoms, headache, or earache
  • Children with known or suspected motion sickness
  • Children with cochlear implants or pacemakers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Day of procedure

Participants use a virtual reality headset starting five minutes before their interventional radiology procedure, continuing through the procedure, and for up to two minutes after the procedure to help reduce pain and anxiety.

1 visit (in-person)

Long-term Monitoring

Duration - 1 hour post-procedure

Participants are observed for changes in pain and anxiety levels up to one hour after the procedure.

1 follow-up visit (in-person or remote)

Trial Site Locations

Total: 1 location

1

Children's Hospital Los Angeles

Los Angeles, California, United States, 90027

Actively Recruiting

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Research Team

S

Saloni M Dangoria

E

Elena Gareau

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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