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Clinical Trials/NCT00739076
NCT00739076
Completed
Not Applicable

Pain Control After Trauma

University of Washington1 site in 1 country184 target enrollmentAugust 2007
ConditionsTrauma

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Trauma
Sponsor
University of Washington
Enrollment
184
Locations
1
Primary Endpoint
Pain and Anxiety
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Using Virtual Reality as a form of pain control for trauma patients.

Detailed Description

The purpose of the study is to investigate the effectiveness of virtual reality (a form of distraction) in order to reduce patients' pain from trauma.

Registry
clinicaltrials.gov
Start Date
August 2007
End Date
December 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

David Patterson

PhD. ABPP. Professor

National Institute of General Medical Sciences (NIGMS)

Eligibility Criteria

Inclusion Criteria

  • Age greater than or equal to 12 years
  • Compliant and able to complete questionnaires
  • Hospitalization for internal injuries requiring a laparotomy or for orthopedic injuries (closed long bone or calcaneus fractures).
  • A minimum of 3 days hospitalization
  • No history of psychiatric (DSM-IV-R Axis I) disorder
  • Not demonstrating delirium, psychosis or any form of Organic Brain Disorder
  • Able to communicate verbally
  • Able to take oral medications
  • Baseline pain level of \>=5/10
  • English-speaking

Exclusion Criteria

  • Age less than 12 years
  • Not capable of indicating pain intensity
  • Not capable of filling out study measures
  • Hospitalization of less than 3 days
  • Evidence of traumatic brain injury
  • History of psychiatric (DSM-IV-R Axis I) disorder as evidenced in the admitting RN and MD admission notes.
  • Demonstrating delirium, psychosis or any form of Organic Brain Disorder and associated memory problems.
  • Unable to communicate orally.
  • Unable to take oral medications
  • History of sig. cardiac, endocrine, neurologic, metabolic, respiratory, gastrointestinal or genitourinary impairment

Outcomes

Primary Outcomes

Pain and Anxiety

Time Frame: up to 3 times a day

Study Sites (1)

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