Actively Recruiting

Phase Not Applicable
Age: 21Years - 70Years
All Genders
Healthy Volunteers
NCT05622344

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

Age: 21Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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