We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov
ClinicalTrials.gov Menu

VRH Pain Reduction During Burn Wound Care and Physical Therapy (VRH)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00260221
Recruitment Status : Completed
First Posted : December 1, 2005
Last Update Posted : May 8, 2013
Sponsor:
Collaborator:
National Institutes of Health (NIH)
Information provided by (Responsible Party):
David R. Patterson, National Institute of General Medical Sciences (NIGMS)

Brief Summary:
Using Virtual Reality Hypnosis to relief pain and anxiety for burn patients.

Condition or disease Intervention/treatment
Burn Behavioral: using VR hypnosis/distraction and audio hypnosis

Detailed Description:
The purpose of the study is to examine whether there is more effective relief of pain and anxiety during wound care procedures in burn-injured patients that are treated with Virtual Reality Hypnosis with post-hypnotic suggestion.

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 77 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Care Provider)
Primary Purpose: Treatment
Official Title: Testing Interactions to Adjunctive Pain Control Techniques
Study Start Date : January 2002
Primary Completion Date : January 2011
Study Completion Date : November 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Burns
U.S. FDA Resources

Arm Intervention/treatment
Experimental: 1
Arm one uses Virtual Reality Hypnosis post hypnotic suggestions to reduce pain durng wound care procedures.
Behavioral: using VR hypnosis/distraction and audio hypnosis
a between subject comparison using VR hypnosis and VR distraction and audio hypnosis for pain control
Experimental: 2
Arm two uses Virtual Reality distraction that is administered at times other than during burn care procedure to control for both for attention and high technology.
Behavioral: using VR hypnosis/distraction and audio hypnosis
a between subject comparison using VR hypnosis and VR distraction and audio hypnosis for pain control
Experimental: 3
Arm three use Audio administered Hypnosis without the visual technology.
Behavioral: using VR hypnosis/distraction and audio hypnosis
a between subject comparison using VR hypnosis and VR distraction and audio hypnosis for pain control



Primary Outcome Measures :
  1. we use GRS, VAS, McGill,and nurse GRS to measure the pain. [ Time Frame: once a day ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   7 Years to 85 Years   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age greater than or equal to 7 years
  • 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:

  • Age less than 7 years
  • Incapable of indicating subjective evaluation of pain
  • Non-English-speaking
  • Demonstrating delirium, psychosis, or Organic Brain Disorder
  • Unable to communicate verbally
  • Significant developmental disability
  • Extreme susceptibility to motion sickness

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00260221


Locations
United States, Washington
University of Washington; Harborview Medical Center
Seattle, Washington, United States, 98104
Sponsors and Collaborators
National Institute of General Medical Sciences (NIGMS)
National Institutes of Health (NIH)
Investigators
Principal Investigator: David R. Patterson, Ph.D. University of Washington

Publications:
Responsible Party: David R. Patterson, PhD. ABPP. Professor, National Institute of General Medical Sciences (NIGMS)
ClinicalTrials.gov Identifier: NCT00260221     History of Changes
Other Study ID Numbers: 19635-B
R01GM042725 ( U.S. NIH Grant/Contract )
First Posted: December 1, 2005    Key Record Dates
Last Update Posted: May 8, 2013
Last Verified: March 2011

Keywords provided by David R. Patterson, National Institute of General Medical Sciences (NIGMS):
Virtual Reality Hypnosis