NCT00261690

Brief Summary

Using Virtual Reality as a form of Distraction during Burn Care.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
184

participants targeted

Target at P75+ for phase_2

Timeline
Completed

Started Feb 2002

Longer than P75 for phase_2

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2002

Completed
3.8 years until next milestone

First Submitted

Initial submission to the registry

December 2, 2005

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 5, 2005

Completed
6.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2012

Completed
Last Updated

April 19, 2013

Status Verified

June 1, 2012

Enrollment Period

10.1 years

First QC Date

December 2, 2005

Last Update Submit

April 17, 2013

Conditions

Burn

Keywords

Virtual Reality Distraction

Outcome Measures

Primary Outcomes (1)

  • We use GRS, McGill to measure the outcome.

    once a day

Study Arms (1)

1

EXPERIMENTAL

Virtual Reality distraction

Behavioral: Virtual Reality Distraction

Interventions

Virtual Reality DistractionBEHAVIORAL

Using virtual reality distraction during a procedure

1

Eligibility Criteria

Age6 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Able to complete subjective evaluations of pain
  • English-speaking
  • Not demonstrating delirium, psychosis, or any form of Organic Brain Disorder
  • Able to communicate orally

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Washington; Harborview Medical Center

Seattle, Washington, 98104, United States

Location

Related Publications (1)

  • Hoffman HG, Patterson DR, Magula J, Carrougher GJ, Zeltzer K, Dagadakis S, Sharar SR. Water-friendly virtual reality pain control during wound care. J Clin Psychol. 2004 Feb;60(2):189-95. doi: 10.1002/jclp.10244.

    PMID: 14724926BACKGROUND

MeSH Terms

Conditions

Burns

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Officials

  • David R. Patterson, Ph.D.

    University of Washington

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
NIH
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD, ABPP. Professor

Study Record Dates

First Submitted

December 2, 2005

First Posted

December 5, 2005

Study Start

February 1, 2002

Primary Completion

March 1, 2012

Study Completion

March 1, 2012

Last Updated

April 19, 2013

Record last verified: 2012-06

Locations

US(1)