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Virtual Reality Water Friendly Wound Care

Water Friendly Virtual Reality for Burns

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02646787
Acronym
H2OWC
Enrollment
56
Registered
2016-01-06
Start date
2015-10-31
Completion date
2020-06-30
Last updated
2020-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

Brief summary

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

Detailed 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.

Interventions

The subject is actively engaged in using virtual reality during a painful burn wound care session.

The subject is passively engaged in using virtual reality during a painful burn wound care session.

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
National Institute of General Medical Sciences (NIGMS)
CollaboratorNIH
University of Texas
CollaboratorOTHER
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
8 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Pain. Pain is measured one time prior a painful burn wound care session, by asking the subjects about their pain level, using a questionnaire called graphic rating scale.one time for the duration of one minute before the wound care
Pain. Pain is measured one time after a painful burn wound, by asking the subjects about their pain level, using a questionnaire called graphic rating scale.one time for the duration of one minute after the wound care

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026