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Virtual Reality Hypnosis for Chronic Pain Reduction (VRHChP)

This study has been completed.
Sponsor:
Collaborator:
National Institute of General Medical Sciences (NIGMS)
Information provided by (Responsible Party):
Shelley A. Wiechman, University of Washington
ClinicalTrials.gov Identifier:
NCT01099657
First received: April 1, 2010
Last updated: May 10, 2017
Last verified: May 2017
April 1, 2010
May 10, 2017
June 2007
May 2012   (Final data collection date for primary outcome measure)
Pain and anxiety [ Time Frame: pre and post VR and then up to one month ]
The subjects will answer questions regarding pain and anxiety at the time of their clinic visit, before and after experiencing virtual reality. Then the subject will be followed for up to one month.
Same as current
Complete list of historical versions of study NCT01099657 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
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Virtual Reality Hypnosis for Chronic Pain Reduction
Virtual Reality Hypnosis for Chronic Pain Reduction
We would like to determine how well hypnosis works when induced through virtual reality medium for patients who have suffered a major burn injury in the past two years and suffer from chronic pain. These patients are coming back to the outpatient burn and plastic clinic at Harborview Medical Center for routine follow-up. We think that patients will find VR-Hypnosis interesting, and it will help them relax and feel less pain.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Care Provider)
Primary Purpose: Treatment
Burns
  • Behavioral: Virtual Reality Hypnosis for chronic pain
    At the time of their clinic visit,the subject will answer pain and anxiety questionnaires before experiencing Virtual Reality Hypnosis. After VRH, the will again answer Pain and anxiety questionnaires.
  • Behavioral: Virtual Reality Distraction for Chronic Pain
    At the time of their clinic visit,the subject will answer pain and anxiety questionnaires before experiencing Virtual Reality Distraction. After VRD, the will again answer Pain and anxiety questionnaires.
  • Experimental: Virtual Reality Hypnosis
    Virtual Reality Hypnosis for chronic pain
    Intervention: Behavioral: Virtual Reality Hypnosis for chronic pain
  • Experimental: Virtual Reality Distraction
    Virtual Reality Distraction for Chronic Pain
    Intervention: Behavioral: Virtual Reality Distraction for Chronic Pain
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
10
May 2012
May 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Age 13 - 75 years
  • Able to complete subjective evaluations of pain
  • English-speaking
  • Able to communicate orally

Exclusion Criteria:

  • Age less than 13 years or greater than 75 years
  • Incapable of indicating subjective evaluation of pain
  • Non-English-speaking (Virtual Reality Hypnosis only available in English)
  • Demonstrating delirium, psychosis, or Organic Brain Disorder
  • Unable to communicate verbally
  • Significant developmental disability
  • Extreme susceptibility to motion sickness
  • Significant head/or neck injury
  • Pregnant women
Sexes Eligible for Study: All
13 Years to 75 Years   (Child, Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01099657
31498
Yes
Not Provided
Plan to Share IPD: Undecided
Shelley A. Wiechman, University of Washington
University of Washington
National Institute of General Medical Sciences (NIGMS)
Not Provided
University of Washington
May 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP