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Clinical Trials/NCT01377454
NCT01377454
Completed
N/A

Wearable Sensor to Detect Postural Instability in People After Mild Traumatic Brain Injury (mTBI)

Oregon Health and Science University1 site in 1 country47 target enrollmentJune 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Brain Concussion
Sponsor
Oregon Health and Science University
Enrollment
47
Locations
1
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of this pilot project is to determine whether using one inertial sensor on the waist during routine clinical balance testing (i.e. Balance Error Scoring System (BESS)), will be a more immediate, objective, reliable and sensitive way to measure and quantify balance deficits in individuals with mild Traumatic Brain Injury (mTBI).

Detailed Description

The purpose of this pilot project is to gather preliminary data to determine whether using one inertial sensor at the waist during the BESS could provide the examiner with a more immediate, objective, reliable and sensitive way to quantify deficits in postural control in the post-concussive population. The investigators hypothesize that the metrics obtained from the iSWAY will be better able to distinguish mTBI subjects from control subjects than the standard clinical assessment. The specific aims are: 1. To determine test-retest and inter-rater reliability of the clinical BESS compared to the instrumented BESS test. 2. To determine if an instrumented BESS can distinguish mTBI from age-matched control subjects better than the commonly used BESS and to determine the best metrics of sway to separate groups.

Registry
clinicaltrials.gov
Start Date
June 2011
End Date
August 2012
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Laurie King

Assistant Professor of Neurology

Oregon Health and Science University

Eligibility Criteria

Inclusion Criteria

  • Have a mild Traumatic Brain Injury or Concussion
  • Between the ages 12-40 years

Exclusion Criteria

  • Out of age range

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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