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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01099657
Other study ID # 31498
Secondary ID
Status Completed
Phase N/A
First received April 1, 2010
Last updated May 10, 2017
Start date June 2007
Est. completion date May 2012

Study information

Verified date May 2017
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date May 2012
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender All
Age group 13 Years to 75 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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.
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.

Locations

Country Name City State
United States Harborview Medical Center Seattle Washington

Sponsors (2)

Lead Sponsor Collaborator
University of Washington National Institute of General Medical Sciences (NIGMS)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain and anxiety 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. pre and post VR and then up to one month
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