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Reducing Brief Thermal and Electrical Pain (Four Study Days)

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Contents

clinicaltrials.gov/study/NCT00682682
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT006826820
Health Conditions in Trial
Pain
Pain
0
Trial Recruitment Size
200
Trial Sponsor
University of Washington
University of Washington
0
Clinical Trial Start Date
2007
0
Primary Completion Date
2008
0
Study Completion Date
2008
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Other0
Interventional Trial Phase
Not Applicable0
Participating Facility
University of Washington
University of Washington
0
Official Name
Reducing Brief Thermal and Electrical Pain (Four Study Days)0
Last Updated
September 13, 2011
0
Allocation Type
Randomized0
Intervention Model
Crossover Assignment0
Masking Type
Single0
Masked Party
Participant0

Other attributes

Intervention Treatment
Virtual Reality video distraction0
Virtual Reality video game0
Study summary

Ultimately, the purpose of the present study is to help improve pain control in burn patients during wound care and physical therapy, where pain levels with opioids alone are often excessively high. This study measures how much virtual reality pain distraction reduces pain compared to traditional opioid pain meds, and whether there is additional pain reduction when Virtual Reality distraction + Opioids are combined. In addition to studying the amount of pain reduction, this study will also measure side effects (if any) of the two treatments (Virtual Reality pain distraction and Opioids) alone and when combined. Healthy volunteers will be recruited from advertisements will undergo a trial of the pain testing. They will receive a series of brief stimuli (at a painful but tolerable safe intensities they select and approve during baseline testing), separated by intervals of no pain. Participants will rate how much pain they felt after each brief stimulus, and will fill out side effects questionnaires after finishing the pain session. Subjects will participate in each of the four conditions in which the order is randomized. * No opioids (0ng/ml hydromorphone) + no virtual reality Snow World distraction * No opioids + yes virtual reality Snow World distraction * Moderate dose of pain medicine (4ng/ml hydromorphone) + no virtual reality * Moderate dose of pain medicine + yes virtual reality Snow World distraction It is our hypothesis that VR distraction + opioids will show a reduced perception of pain in subjects more than opioids alone or no intervention (control).

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