Virtual Reality Pain Control During Burn Wound Care

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

184 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-02-28

Study Completion Date

2012-03-31

Brief Summary

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Using Virtual Reality as a form of Distraction during Burn Care.

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Detailed Description

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The purpose of the study is to investigate the effectiveness of virtual reality (a form of distraction) in order to reduce patients' procedural burn pain.

Conditions

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Burn

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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1

Virtual Reality distraction

Group Type EXPERIMENTAL

Virtual Reality Distraction

Intervention Type BEHAVIORAL

Using virtual reality distraction during a procedure

Interventions

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Virtual Reality Distraction

Using virtual reality distraction during a procedure

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Able to complete subjective evaluations of pain
* English-speaking
* Not demonstrating delirium, psychosis, or any form of Organic Brain Disorder
* Able to communicate orally

Exclusion Criteria

* Incapable of indicating subjective evaluation of pain
* Non-English-speaking
* Severe head or neck injury or other medical conditions that prohibit patient from wearing VR helmet
* Demonstrating delirium, psychosis, or Organic Brain Disorder
* Unable to communicate verbally
* Significant developmental disability
* Extreme susceptibility to motion sickness
* Reports having no problem with pain during wound care.

Minimum Eligible Age

6 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No