Virtual Reality Pain Control During Burn Wound Care (VRPT/H2O/RT)
This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
David R. Patterson, National Institute of General Medical Sciences (NIGMS)
ClinicalTrials.gov Identifier:
NCT00261690
First received: December 2, 2005
Last updated: April 17, 2013
Last verified: June 2012
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Purpose
Using Virtual Reality as a form of Distraction during Burn Care.
| Condition | Intervention | Phase |
|---|---|---|
|
Burn |
Behavioral: Virtual Reality Distraction |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Use of Virtual Reality for Adjunctive Treatment of Burn Pain |
Resource links provided by NLM:
Further study details as provided by National Institute of General Medical Sciences (NIGMS):
Primary Outcome Measures:
- We use GRS, McGill to measure the outcome. [ Time Frame: once a day ] [ Designated as safety issue: No ]
| Enrollment: | 184 |
| Study Start Date: | February 2002 |
| Study Completion Date: | March 2012 |
| Primary Completion Date: | March 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Virtual Reality distraction
|
Behavioral: Virtual Reality Distraction
Using virtual reality distraction during a procedure
|
Detailed Description:
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.
Eligibility| Ages Eligible for Study: | 6 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
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.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00261690
Locations
| United States, Washington | |
| University of Washington; Harborview Medical Center | |
| Seattle, Washington, United States, 98104 | |
Sponsors and Collaborators
Investigators
| Principal Investigator: | David R. Patterson, Ph.D. | University of Washington |
More Information
Publications:
Garcia-Palacios, A., Hoffman, H.G., Cain, V., Tininenko, J., Schmidt, A., Villa-Martin, H., and Patterson, D.R., (2004). Using virtual reality to help reduce pain during severe burn wound-care procedures. In MacLachlan, M., and Gallagher, P., Eds Enabling Technologies: Body Image and Body Function. Churchill Livingstone, Edinburgh England. Hoffman, H.G., Patterson, D.R., Magula, J., Carrougher, G.J. Zeltzer, K. Dagadakis, S., & Sharar, S. R. (2004). Water-friendly virtual reality pain control during wound care. Journal of Clinical Psychology, 60, 1-7.
| Responsible Party: | David R. Patterson, PhD, ABPP. Professor, National Institute of General Medical Sciences (NIGMS) |
| ClinicalTrials.gov Identifier: | NCT00261690 History of Changes |
| Other Study ID Numbers: | 13289-C, R01 GM042725 |
| Study First Received: | December 2, 2005 |
| Last Updated: | April 17, 2013 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute of General Medical Sciences (NIGMS):
|
Virtual Reality Distraction |
Additional relevant MeSH terms:
|
Burns Wounds and Injuries |
ClinicalTrials.gov processed this record on May 22, 2013