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VR High Tech Pain Control Burn Wound Care

High Technology Pain Control During Burn Wound Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02427659
Acronym
VRH2O
Enrollment
8
Registered
2015-04-28
Start date
2011-11-30
Completion date
2017-08-31
Last updated
2019-03-13

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

Conditions

Burn, Pain

Keywords

VRD, Virtual Reality as Distraction during Procedure, Burn Wound Care

Brief summary

Using virtual reality as a form of distraction for pain during wound care. Virtual reality involves looking into a set of goggles and then moving through a computer-simulated world.

Detailed description

This study has three different groups. Patients will be randomly assigned to one of three groups (two treatments and one control). Treatment for Group 1 is Virtual Reality Distraction during wound care. Group 2 will listen to an audio recording called Sounds of Nature. Group 3 will be the control group. Subjects in all three groups will receive the following questionnaires: Graphic Rating Scale McGill Short-Form pain questionnaire Sullivan Catastrophization scale (only on Day 1/Baseline) The Nurse GRS

Interventions

BEHAVIORALVirtual Reality Distraction

The subjects will receive a 20-minute Virtual Reality Distraction (VRD) during their wound care procedure. The nurse will be doing their wound care.

BEHAVIORALAudio (sound of nature)

The subjects will listen to an audio recording called Sounds of Nature during their wound care.

The subjects will receive their standard care during wound care. The nurse will be doing the wound care.

Sponsors

National Institute of General Medical Sciences (NIGMS)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Caregiver)

Eligibility

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

Inclusion criteria

* Age greater than or equal to 18 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 18 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 frameDescription
Pain as measured by McGill Short Form Pain Questionnaireup to an hourPain is being measured
Pain as measured by Nurse Graphic Rating Scaleup to 3 hoursPain is being measured.
Pain and anxiety as measured by Graphic Rating Scaleup to an hourPain and anxiety is being measured

Countries

United States

Outcome results

None listed

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