- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03491657
Virtual Reality Analgesia for Pediatric Burn Survivors
July 9, 2018 updated by: The University of Texas Medical Branch, Galveston
Many children with large severe burns report severe pain during burn wound cleaning.
The current study explores whether adjunctive immersive Virtual Reality distraction may help reduce the intensity of pain experienced by children during burn wound cleaning by taking the patient's mind off their pain.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
All patients always receive their usual pain medications.
Using a within-subjects, within-wound care design, in the current study, pediatric patients being treated for severe burn injuries will receive music distraction during some portions of their wound care (active comparator condition), and they will receive what we predict will be an unusually strong distraction, immersive virtual reality (the experimental treatment) during other comparable portions of the same wound cleaning sessions.
During virtual reality, each patient will look into virtual reality goggles, and will play a simple cartoon-like virtual reality game SnowWorld during burn wound cleaning.
After each wound care session, the patient will rate how much pain they experienced during wound care during No VR (music only) compared to how much pain they experienced during wound care during virtual reality, on each study day, for up to 10 study days per patient.
Treatment order randomized.
Study Type
Interventional
Enrollment (Actual)
62
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Texas
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Galveston, Texas, United States, 77550
- Shriners Hospital for Children; Shriners Burns Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 years to 17 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion criteria:
- Compliant and able to complete subjective evaluations,
- A minimum of 10% of total burned surface area,
- No history of psychiatric (DSM-III-R Axis I) disorder(s),
- Not demonstrating delirium, psychosis or any form of organic brain disorder,
- Able to communicate verbally in English or Spanish,
- Admitted to UTMB/Shriners, 6-17 years of age.
Exclusion criteria:
- No wound cleaning sessions required.
- Less than 10% of total burned surface area.
- History of psychiatric (DSM-III-R Axis I) disorder(s).
- Demonstrating delirium, psychosis or organic brain disorder.
- Unable to communicate verbally in English or Spanish.
- History of significant cardiac, endocrine, neurologic, metabolic, respiratory, gastrointestinal, or genitourinary impairment.
- Receiving prophylaxis for alcohol or drug withdrawal,
- Developmental disability, Younger than 6 years; older than 17 years,
- Burns of eyes, eyelids or face so severe they preclude the use of VR,
- Worst pain intensity of less than 5 on a 0 to 10 scale, during baseline No VR wound care Day 1.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: virtual reality distraction (Yes VR)
In addition to their standard pain medications, patients will play a virtual realty game named SnowWorld during some portions of their burn wound cleaning procedure, on each study day.
|
|
|
Active Comparator: music distraction (No VR condition)
In addition to their standard pain medications, patients will listen to music during comparable portions of their burn wound cleaning procedure, on each study day.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
"Worst Pain" rating of pain intensity during Music vs. during VR
Time Frame: measured after burn wound care on each study day for up to 10 study days per patient
|
worst pain during wound care.
This single question measures the sensory component of pain during wound care.
Patients will rate their "worst pain" during burn wound care.
on a zero to ten scale, where zero is "no pain at all " and 10 is "excruciating pain".
Lower scores represent better outcome.
No subscales.
|
measured after burn wound care on each study day for up to 10 study days per patient
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Graphic Rating Scale "Time spent thinking about pain" during Music vs. during VR
Time Frame: measured after burn wound care on each study day for up to 10 study days per patient
|
This single question measures the Cognitive component of pain during wound care.
Patients will rate how much time they spent thinking about pain during burn wound care, on a zero to ten scale, where zero is "no time at all" and 10 is "the entire time".
Lower scores represent better outcome.
No subscales.
|
measured after burn wound care on each study day for up to 10 study days per patient
|
|
Graphic Ratings Scale measure of pain unpleasantness during Music vs. during VR
Time Frame: measured after woundcare on each study day for up to 10 study days per patient
|
This single question measures the emotional component of pain.
On a scale from zero to ten, where zero is "not unpleasant at all", 10 is "excruciatingly unpleasant".
Lower scores represent better outcome.
No subscales.
|
measured after woundcare on each study day for up to 10 study days per patient
|
|
Graphic Rating Scale "Fun" during Music vs. during VR
Time Frame: measured after wound care on each study day for up to 10 study days per patient
|
This single question measures positive affect during burn wound care.
On a zero to ten scale, where zero is no fun at all and 10 is extremely fun.
Higher scores represent better outcome.
No subscales.
|
measured after wound care on each study day for up to 10 study days per patient
|
|
Graphic Rating Scale Satisfaction with pain management during Music vs. during VR
Time Frame: Measured after wound care on Study Day 1.
|
This single question measures how satisfied the patient is with how well their pain was controlled during burn wound care.
Higher scores represent better ourcomes.
No subscales
|
Measured after wound care on Study Day 1.
|
|
Child Health Questionnaire
Time Frame: measured at 0, 9 months and 12 month followup visits
|
Child Health Questionnaire The Child Health Questionnaire (CHQ) is a family of generic QOL instruments.
The CHQ includes 87 scales that consider the effects of children's health on family functioning, and specific scales such as behavior and self-esteem.
The CHQ measures 14 unique physical and psychosocial concepts.
Questionnaires will be self-completed by the outpatients or parents, or both.
Raw scores will converted to scaled scores from zero to 100.
Higher scores indicate better health and better quality of life outcome.
|
measured at 0, 9 months and 12 month followup visits
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sullivans Pain Catastrophizing Scale for Children (Crombez et al., 2003).
Time Frame: measured on Study day 1
|
High catastrophizers are people who have unusually negative emotions and pessimistic beliefs about their ability to deal with the upcoming pain.
Higher scores indicate worse outcome.
13 items, ratings from zero to 5 per item, 65 total points possible, 6 items measure helplessness, 3 items measure magnification, 4 items measure rumination subscores = 0-30 for helplessness, 0-15 for magnification, 0-20 for rumination.
The PCS total score is calculated by summing the 13-item responses, and provides a good index of the catastrophizing construct through the inclusion of highly correlated subscales of helplessness, rumination, and magnification.
Higher scores on the PCS are indicative of greater pain-related catastrophizing.
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measured on Study day 1
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Walter J Meyer, MD, UTMB/Shriners
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Crombez G, Bijttebier P, Eccleston C, Mascagni T, Mertens G, Goubert L, Verstraeten K. The child version of the pain catastrophizing scale (PCS-C): a preliminary validation. Pain. 2003 Aug;104(3):639-646. doi: 10.1016/S0304-3959(03)00121-0.
- Hoffman HG, Chambers GT, Meyer WJ 3rd, Arceneaux LL, Russell WJ, Seibel EJ, Richards TL, Sharar SR, Patterson DR. Virtual reality as an adjunctive non-pharmacologic analgesic for acute burn pain during medical procedures. Ann Behav Med. 2011 Apr;41(2):183-91. doi: 10.1007/s12160-010-9248-7.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 13, 2014
Primary Completion (Actual)
January 3, 2017
Study Completion (Actual)
January 3, 2017
Study Registration Dates
First Submitted
March 10, 2018
First Submitted That Met QC Criteria
March 31, 2018
First Posted (Actual)
April 9, 2018
Study Record Updates
Last Update Posted (Actual)
July 11, 2018
Last Update Submitted That Met QC Criteria
July 9, 2018
Last Verified
March 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 71011-GAL
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
No IPD will be shared with other researchers.
Any data shared with other researchers will be in unidentifiable form.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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