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Reducing Adult Inpatients Anxiety With Virtual Reality Meditation

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Stanford University

Status

Begins enrollment in 3 months

Conditions

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 the study is to evaluate if non-invasive, distracting devices (virtual reality) can decrease anxiety and improve affect and satisfaction in adult, hospitalized patients.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • between age 18-99
  • hospitalized at Stanford Health Care
  • english-speaking

Exclusion criteria

  • significant cognitive impairment or inability to consent
  • current nausea
  • visual problems or currently using corrective glasses that are incompatible with the virtual reality headset
  • a history of severe motion sickness
  • a history of seizures cause by flashing light
  • clinically unstable or require immediate/urgent intervention

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 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

Thomas Caruso; Man Yee Suen

Data sourced from clinicaltrials.gov

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