Virtual Reality Hypnosis for Chronic Pain Reduction

NCT ID: NCT01099657

Last Updated: 2017-05-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-06-30

Study Completion Date

2012-05-31

Brief Summary

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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.

Detailed Description

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Conditions

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Burns

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Caregivers

Study Groups

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Virtual Reality Hypnosis

Virtual Reality Hypnosis for chronic pain

Group Type EXPERIMENTAL

Virtual Reality Hypnosis for chronic pain

Intervention Type BEHAVIORAL

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

Virtual Reality Distraction for Chronic Pain

Group Type EXPERIMENTAL

Virtual Reality Distraction for Chronic Pain

Intervention Type BEHAVIORAL

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.

Interventions

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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.

Intervention Type 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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

13 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute of General Medical Sciences (NIGMS)

NIH

Sponsor Role collaborator

University of Washington

OTHER

Sponsor Role lead

Responsible Party

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Shelley A. Wiechman

Associate Professor, Rehabilitative Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Harborview Medical Center

Seattle, Washington, United States

Site Status

Countries

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United States

Other Identifiers

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31498

Identifier Type: -

Identifier Source: org_study_id

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