Actively Recruiting
StableEyes With Active Neurofeedback
Led by Johns Hopkins University · Updated on 2025-11-10
48
Participants Needed
2
Research Sites
216 weeks
Total Duration
On this page
Sponsors
J
Johns Hopkins University
Lead Sponsor
N
National Aeronautics and Space Administration (NASA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
StableEyes With Active Neurofeedback
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed and dated informed consent form provided
- Willing to comply with all study procedures and available for the study duration
- In good general health or diagnosed with unilateral vestibular schwannoma
- Willing to follow the SWAN device and/or vestibular rehabilitation exercises
You will not qualify if you...
- Currently using anti-nausea medication
- Cervical spine problems limiting head motion to less than 30 degrees in horizontal or vertical planes
- Orthopedic conditions preventing independent walking or standing
- Legal blindness with visual acuity of 20/200 or worse
- Treatment with investigational motion sickness drugs or behavioral interventions within the past 30 days
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Johns Hopkins University
Baltimore, Maryland, United States, 21287
Actively Recruiting
2
Naval Medical Research Unit
Dayton, Ohio, United States, 45433
Enrolling by Invitation
Research Team
M
Michael Schubert, PhD
CONTACT
M
Matthew Stewart, MD PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
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