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Virtual Reality (VR) for Prone Pain Procedures

University of California (UC) Davis logo

University of California (UC) Davis

Status

Completed

Conditions

Anxiety
Pain
Virtual Reality

Treatments

Other: Virtual Reality Headset

Study type

Interventional

Funder types

Other

Identifiers

NCT05615675
1919687

Details and patient eligibility

About

The purpose of this study is to evaluate the effectiveness of virtual reality (VR) distraction in patients undergoing interventional pain procedures in the prone position. VR has been shown to improve patient experience during interventional pain procedures, however, many of these procedures are done in the prone position making VR a challenge. This study will evaluate the effect of a VR headset and support in patients undergoing prone interventional pain procedures compared to control.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18 years old or older, who are referred to University of California Davis Pain Medicine Clinic and require an interventional pain procedure
  • English speaking and with the ability to understand oral and written instructions

Exclusion criteria

  • Pregnant women
  • Prisoners
  • Patients who have high risk of motion sickness, seizure disorder, or visual/hearing impairment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Virtual Reality
Experimental group
Description:
Patients undergo prone pain procedure with virtual reality distraction
Treatment:
Other: Virtual Reality Headset
Control
No Intervention group
Description:
Patients undergo prone pain procedure without virtual reality distraction

Trial contacts and locations

1

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Central trial contact

Amaad Sulahria, DO; Michael Jung, MD MBA

Data sourced from clinicaltrials.gov

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