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Clinical Trial Summary

The investigators have developed a self-administered rehabilitation tool that incrementally guides the user to increase head motion to mitigate motion sickness and enhance postural recovery following centrifugation or unilateral vestibular nerve deafferentation surgery.


Clinical Trial Description

The rehabilitation device guides users to perform sinusoidal head rotations, matched to a metronome, about the yaw, pitch, and roll axes (60 sec epochs, 5 minutes per axis, 15 min total). The assessment for each axis consists of the number of completed epochs with each epoch requiring head rotations of a different amplitude. Subjects are instructed to begin with an 'easy' amplitude (i.e. small) and increase or decrease amplitude depending on the subject's perception of motion sickness - which is input from 0 (absent motion sick) to 11 (vomit) using a handheld controller. Video-oculography captures eye and head velocity as well as tracks the number of blinks and saccades, metrics that can indicate worsening nausea. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05622344
Study type Interventional
Source Johns Hopkins University
Contact Michael Schubert, PhD
Phone 4108427403
Email mschube1@jhmi.edu
Status Recruiting
Phase N/A
Start date August 8, 2022
Completion date September 30, 2025

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