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Treatment of Parental Anxiety Virtual Reality (VR)

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Stanford University

Status

Enrolling

Conditions

Parents
Anxiety
Virtual Reality

Treatments

Behavioral: Virtual Reality headset with calming scenery

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to determine if non-invasive distracting devices (Virtual Reality headset) are more effective than the standard of care (i.e., no technology based distraction) for preventing anxiety in parental and pediatric populations

Enrollment

500 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Ages 18-99 (Parents whose children is hospitalized)
  • Able to consent
  • Parents whose child is undergoing various procedures at LPCH and Stanford Hospital and Clinics.

Exclusion criteria

  • People who do not consent
  • Significant Cognitive Impairment
  • History of Severe Motion Sickness
  • Current Nausea
  • Seizures
  • Visual Problems
  • Patients whose children are clinically unstable or require urgent/emergent intervention

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

500 participants in 2 patient groups

Virtual Reality
Experimental group
Description:
Participants will be immersed in a virtual environment. Calming scenery will be shown via the headset for 20-30 minutes
Treatment:
Behavioral: Virtual Reality headset with calming scenery
Control
No Intervention group
Description:
No intervention (i.e. virtual reality headset) will be applied to the participant.

Trial contacts and locations

1

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Central trial contact

Man Yee Suen, MMed; Thomas J Caruso, MD

Data sourced from clinicaltrials.gov

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