Dizziness Clinical Trial
Official title:
Vestibular Testing: Consistency and Effects Over Time
Verified date | April 2022 |
Source | University of Miami |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this study is to test the consistency and repeatability of a portable goggle system for testing optokinetic, ocular, and reaction time. The study examines the day to day consistency, time of day and learning effects as well as any secondary motion sickness.
Status | Completed |
Enrollment | 78 |
Est. completion date | November 28, 2016 |
Est. primary completion date | November 28, 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Age 18 to 65 - Both Females and males - Staff and students at all levels at the University of Miami or first-degree - relatives/significant others of those individuals. Exclusion Criteria: - History of vestibular disorder/dysfunction - Central processing disorder - Impaired vision without corrective lenses (max 20/60 uncorrected) - Moderate to severe hearing loss [>55 decibel (dB) Pure Tone Average (PTA), <50% word identification] |
Country | Name | City | State |
---|---|---|---|
United States | University of Miami Miller School of Medicine | Miami | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Miami |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Vestibular Reaction Times | Repeatability, variation and learning effect of vestibular testing of PAS goggles will be evaluated using the test results on both sessions for the following sub-tests: a) Visual Reactive Time (VRT), b) Saccades and Reaction Time (SRT) Saccade Latency, c) SRT Motor Latency, and d) Auditory Reaction Time (ART). ART, VRT and SRT subtests are all evaluated in msec. | 2 Days | |
Primary | Vestibular Subjective Visual Vertical | Repeatability, variation and learning effect of vestibular testing of PAS goggles will be evaluated using the test results on both sessions for the Subjective Visual Vertical sub-test assessed in degrees. | 2 Days | |
Primary | Vestibular Smooth Pursuit Horizontal | Repeatability, variation and learning effect of vestibular testing of PAS goggles will be evaluated using the test results on both sessions for the Smooth Pursuit Horizontal (SPH) sub-tests in degree squared per second. | 2 Days | |
Primary | Vestibular Percentage of Saccade | Repeatability, variation and learning effect of vestibular testing of PAS goggles will be evaluated using the test results on both sessions for the sub-tests Smooth Pursuit Horizontal (SPH) evaluated as percentage of saccades completed. | 2 Days | |
Primary | Vestibular Anti-Saccade | Repeatability, variation and learning effect of vestibular testing of PAS goggles will be evaluated using the test results on both sessions for the Anti-saccade sub-test evaluted in Percent Error. | 2 Days | |
Primary | Vestibular Gain | Repeatability, variation and learning effect of vestibular testing of PAS goggles will be evaluated using the test results on both sessions for the following sub-tests: a) OKN at 60 degrees/second, and b) Smooth Percent Horizontal Velocity. Subtests are all evaluated in gain (output/input in decimal form) | 2 Days | |
Primary | Vestibular Saccade Horizontal | Repeatability, variation and learning effect of vestibular testing of PAS goggles will be evaluated using the test results on both sessions for the Saccade Horizontal sub-tests evaluated in seconds. | 2 Days | |
Primary | Vestibular Predictive Saccade | Repeatability, variation and learning effect of vestibular testing of PAS goggles will be evaluated using the test results on both sessions for the subtest Predictive Saccade (PS) evaluated as percentage of prediction. | 2 Days | |
Primary | Motion Sickness as Measured by the MSAQ | Motion sickness is measured by the subjects being given a motion sickness assessment questionnaire (MSAQ). The MSAQ is a validated measure of motion sickness and in this questionnaire the examiner asks subjects 16 questions. Subjects score each question as "not at all" (score of zero) or on a seventy scale of 1-9. The total score ranging from 0-144 with the score reported as a percentage. The higher percentage score indicates more motion symptoms experienced by the subjects. | Day 1 |
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