The Effect of Rhythmic Auditory Stimulation on VOR Gain Adaptation Among Healthy Adults - A Randomized Clinical Trial "VOR - Vestibulo-ocular Reflex" (VOR)

April 30, 2026 updated by: University of Haifa

Dancing Eyes: The Effect of Rhythmic Auditory Stimulation on VOR Gain Adaptation Among Healthy Adults - A Randomized Clinical Trial

The goal of this study is to learn whether adding rhythmic sound (a metronome beat or music) to eye-head exercises can improve the reflex that keeps vision clear during head movement. This reflex, called the vestibulo-ocular reflex (VOR), helps maintain visual stability during activities such as walking, turning, or bending. This type of training may help people with dizziness or balance problems, but this study focuses on healthy adults.

The main questions addressed are:

Does performing VOR exercises with a steady metronome beat improve the VOR more than performing the same exercises in silence?

Does performing the exercises while listening to self-selected rhythmic music also improve the VOR, and is the effect better or worse than a metronome?

Do the different sound conditions change how difficult the training feels or how dizzy participants feel?

Three conditions will be compared:

Silence: standard VOR training with no sound Metronome: training timed to a simple, steady beat Music: training performed while listening to self-selected music with a clear beat

The study will assess whether adding rhythmic sound leads to greater improvement in VOR gain and whether one type of sound is more effective than another.

Participants are healthy adults. Participants will:

Attend the laboratory for three separate visits, each with a different sound condition (silence, metronome, and music).

Visits will be at least 48 hours apart.

Wear specialized goggles that record eye and head movements (EyeSeeCam).

Perform brief eye-head tests before and after training, consisting of rapid head turns while maintaining fixation on a visual target.

Complete 15 minutes of Incremental VOR adaptation training during each visit, repeating rapid head turns while fixating on a laser projected target (StableEyes). In some sessions movements will be synchronized to a metronome or music.

Rate perceived training difficulty, ease of following the rhythm, and any dizziness or discomfort.

By comparing results across the three conditions within the same participants, the study will determine whether a simple, low-cost rhythmic cue can enhance the effects of standard VOR exercises without increasing discomfort.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

12

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ramat Gan, Israel, 5300419
        • Sheba Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy

Exclusion Criteria:

  • Vestibular disorders. Neurologic conditions, Deafness, Blindness

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Silence
Complete 15 minutes of vestibular adaptation training in silent condition
15 minutes of vestibular adaptation training without any background noise.
Experimental: Metronome
15 minutes of vestibular adaptation training with metronome beat played in the background
the same 15 minutes of vestibular adaptation training will be completed by all participants in 3 different conditions: silence, metronome, and music. participants will be instructed to synchronize their head impulses to the beat in the auditory conditions.
Experimental: Music
15 minutes of vestibular adaptation training with music played in the background
the same 15 minutes of vestibular adaptation training will be completed by all participants in 3 different conditions: silence, metronome, and music. participants will be instructed to synchronize their head impulses to the beat in the auditory conditions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in horizontal semicircular canal VOR gain for active and passive head impulses
Time Frame: Gains values- Baseline (pre-training) and immediately after each training session (post-training). Assessed during each of the three sessions. The sessions are separated by at least 48 hours and all three will be completed over approximately 2 - 4 weeks.
The change in vestibulo-ocular reflex (VOR) gain for the horizontal semicircular canals, measured using video head impulse testing (vHIT), calculated as the difference between pre-training and post-training gain values for both active and passive head impulses under each auditory condition (Silence, Metronome, and Music).
Gains values- Baseline (pre-training) and immediately after each training session (post-training). Assessed during each of the three sessions. The sessions are separated by at least 48 hours and all three will be completed over approximately 2 - 4 weeks.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-reported training difficulty and adverse symptoms
Time Frame: Immediately after completion of each of the three training sessions. Sessions will be separated by at least 48 hours and all three will be completed over approximately 2-4 weeks.
Participant-reported ratings of training difficulty and adverse symptoms (including dizziness and nausea), assessed using 1-10 visual analog scales completed after each training session under each of the three auditory conditions.
Immediately after completion of each of the three training sessions. Sessions will be separated by at least 48 hours and all three will be completed over approximately 2-4 weeks.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 15, 2025

Primary Completion (Actual)

February 1, 2026

Study Completion (Actual)

February 20, 2026

Study Registration Dates

First Submitted

December 15, 2025

First Submitted That Met QC Criteria

January 8, 2026

First Posted (Actual)

January 16, 2026

Study Record Updates

Last Update Posted (Actual)

May 1, 2026

Last Update Submitted That Met QC Criteria

April 30, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • SMC-0074-23

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

Yes

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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