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Virtual Reality Water Friendly Wound Care (H2OWC)

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University of Washington

Status

Completed

Conditions

Pain

Treatments

Behavioral: Active Virtual Reality
Behavioral: Passive Virtual Reality

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02646787
R01GM042725 (U.S. NIH Grant/Contract)
STUDY00002594

Details and patient eligibility

About

Using virtual reality as a form of distraction during a painful burn wound care procedure in addition to pain medication.

Full description

Using virtual reality as a form of distraction during a painful burn wound care procedure in addition to pain medication.The aim of this study is to conduct a randomized controlled trial of Virtual Reality as a means to reduce pain during wound care in patients hospitalized for their burn injuries at Harborview Medical Center Burn Center, and Shriners Hospitals for Children in Galveston, Texas.

Enrollment

56 patients

Sex

All

Ages

8+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age greater than or equal to 8 years
  • Compliant and able to complete questionnaires
  • No history of psychiatric disorder
  • Not demonstrating delirium, psychosis or any form of Organic Brain Disorder
  • Able to communicate verbally
  • English-speaking

Exclusion criteria

  • Age less than 8 years
  • Not capable of indicating pain intensity
  • Not capable of filling out study measures
  • Evidence of traumatic brain injury
  • History of psychiatric disorder
  • Demonstrating delirium, psychosis or any form of Organic Brain Disorder and associated memory problems
  • Unable to communicate orally
  • Receiving prophylaxis for alcohol or drug withdrawal
  • Developmental disability
  • Any face/head/neck injuries that interfere with the use of Virtual Reality equipment
  • Non-English Speaking
  • Extreme susceptibility to motion sickness
  • Seizure history

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

56 participants in 3 patient groups

Active Virtual Reality
Experimental group
Description:
The subject is actively engaged in using virtual reality during a painful burn wound care session.
Treatment:
Behavioral: Active Virtual Reality
Passive Virtual Reality
Experimental group
Description:
The subject is passively engaged in using virtual reality during a painful burn wound care session.
Treatment:
Behavioral: Passive Virtual Reality
Control
No Intervention group
Description:
No intervention during the subject's standard wound care session

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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