Clinical trial Recruiting at 1 site Interventional Ages 21 to 70

Self-administered rehabilitation for motion sickness and vestibular disorders

Official title: StableEyes With Active Neurophysiological Feedback

Run by Johns Hopkins University · NCT05622344 · Data updated 2026-11-12

This study tests a self-guided rehab tool to see if it can help people with motion sickness and balance issues feel better by practicing head movements.

More Vestibular Disorder trials

Quick facts

Study typeInterventional
Ages21 Years to 70 Years
SexAll
Enrollment48 (estimated)
SponsorJohns Hopkins University
Academic / other
Locations2 sites (Baltimore, Maryland and 1 other locations)
StatusRecruiting
StartedAugust 8, 2022
Main results expectedMarch 30, 2027
Study endsMarch 30, 2027
Registry record updatedSeptember 8, 2026
Trial IDNCT05622344 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include individuals diagnosed with unilateral vestibular schwannoma or those experiencing vestibular disorders who are in good general health.

Probably not a fit

Patients currently using anti-nausea medication or those with significant orthopedic or visual impairments may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates a self-administered rehabilitation tool designed to help individuals with vestibular disorders, including vestibular schwannoma and motion sickness. Participants will perform guided head rotations in a structured manner, adjusting the amplitude based on their perception of motion sickness. The device tracks eye and head movements to assess the effectiveness of the rehabilitation. The goal is to enhance postural recovery and reduce symptoms of motion sickness through incremental training.

Why it matters

Potential benefit: If successful, this approach could significantly improve the quality of life for patients suffering from motion sickness and vestibular disorders.

How similar studies have gone: While similar approaches have been explored, this specific method of self-guided rehabilitation using neurofeedback is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Provision of signed and dated informed consent form
2. Stated willingness to comply with all study procedures and availability for the duration of the study
3. In good general health as evidenced by medical history or diagnosed with unilateral vestibular schwannoma
4. Willing to adhere to the SWAN and/or vestibular rehabilitation regimen

Exclusion Criteria:

1. Current use of anti-nausea medication
2. Presence of cervical spine pathology that limits head motion to \< 30 degrees in the horizontal or vertical plane (i.e. degenerative disc disease, rheumatoid arthritis)
3. Any orthopedic pathology that prevents walking or standing independently (i.e. recent surgery)
4. Legal blindness (20/200 or worse visual acuity)
5. Treatment using a motion sickness investigational drug or other motion sickness behavioral intervention within 30 days

Where it's running

  • Johns Hopkins University
    Baltimore, Maryland, United States
    Recruiting
  • Naval Medical Research Unit
    Dayton, Ohio, United States
    Enrolling by invitation

Study contacts

  • Principal investigator: Matthew Stewart, MD PhD — Johns Hopkins University
  • Study coordinator: Michael Schubert, PhD
  • Email: mschube1@jhmi.edu
  • Phone: 4108427403

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.