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Virtual reality could help pinpoint the perfect exercise dose for dizziness relief

NCT ID NCT04851184

Symptom relief Sponsor: George Washington University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aimed to find the best amount of exercise needed to improve dizziness symptoms in people with balance disorders. Researchers used virtual reality (VR) to measure how much exercise helps and compared VR exercises to standard physical therapy. The study included people with different types of dizziness and healthy volunteers for comparison.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

28 people

The number who actually took part.

Started

Mar 2021

Finished

Sep 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 74 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Known or suspected vestibular dysfunction * Healthy volunteers without dizziness to serve as healthy control subjects Exclusion Criteria: * Previous cerebrovacular accident (stroke) * Reported neurologic or oculuomotor disease * Taking of medications that affect the vestibular or oculomotor system. * Current symptoms of benign paroxysmal positional hypofunction * Concussion occuring less than 7 days prior to enrollment in this study * Currently pregnant, or plan to become pregnant during the timeline of the study * Chronic kidney disease * COPD * Known coronary artery disease or cardiomyopathy * immunocompromised state from a solid organ transplant * Severe Obesity as defined by BMI of greater than or equal to 40 kg/m2 * Sickle cell disease

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Conditions

The condition(s) this trial relates to.

idiopathic bilateral vestibulopathy unilateral hypoactive labyrinth vestibular disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Vestibular disorder

Contacts and locations

Locations

  • The George Washington University, Department of Health, Human Function and Rehabilitation Science

    Washington D.C., District of Columbia, 20006, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.