Study Results
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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COMPLETED
NA
8 participants
INTERVENTIONAL
2011-11-30
2017-08-31
Brief Summary
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Detailed Description
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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
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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Virtual 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.
Virtual 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.
Audio (sounds of nature)
The subjects will listen to an audio recording called "Sounds of Nature" during their wound care. The nurse will be doing the wound care.
Audio (sound of nature)
The subjects will listen to an audio recording called "Sounds of Nature" during their wound care.
control standard nurse wound care
The subjects will receive their standard care during wound care. The nurse will be doing the wound care.
Control standard nurse wound care
The subjects will receive their standard care during wound care. The nurse will be doing the wound care.
Interventions
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Virtual 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.
Audio (sound of nature)
The subjects will listen to an audio recording called "Sounds of Nature" during their wound care.
Control standard nurse wound care
The subjects will receive their standard care during wound care. The nurse will be doing the wound care.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
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National Institute of General Medical Sciences (NIGMS)
NIH
Responsible Party
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David R. Patterson
Professor
Principal Investigators
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David R. Patterson, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University fo Washington
Locations
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University of Washington; Harborview Medical Center
Seattle, Washington, United States
Countries
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Other Identifiers
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41673
Identifier Type: -
Identifier Source: org_study_id
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