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Clinical Trials/NCT02427659
NCT02427659
Completed
Not Applicable

High Technology Pain Control During Burn Wound Care

National Institute of General Medical Sciences (NIGMS)1 site in 1 country8 target enrollmentNovember 2011
ConditionsPainBurn

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
National Institute of General Medical Sciences (NIGMS)
Enrollment
8
Locations
1
Primary Endpoint
"Pain and anxiety" as measured by Graphic Rating Scale
Status
Completed
Last Updated
7 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
November 2011
End Date
August 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
National Institute of General Medical Sciences (NIGMS)
Responsible Party
Principal Investigator
Principal Investigator

David R. Patterson

Professor

National Institute of General Medical Sciences (NIGMS)

Eligibility Criteria

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

Outcomes

Primary Outcomes

"Pain and anxiety" as measured by Graphic Rating Scale

Time Frame: up to an hour

Pain and anxiety is being measured

"Pain" as measured by McGill Short Form Pain Questionnaire

Time Frame: up to an hour

Pain is being measured

"Pain" as measured by Nurse Graphic Rating Scale

Time Frame: up to 3 hours

Pain is being measured.

Study Sites (1)

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