ACTIVE_NOT_RECRUITING

The Effect of Bone-Conducted Stimulation on Rotary Chair Time Constants in Patients With Vestibular Migraines

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to learn if the Otolith Labs device can improve vestibular function of subjects with vestibular migraine. The main questions it aims to answer are: * When the Otolith Labs device is on, are objective measures of the vestibular system better than when the device is off? * When the Otolith Labs device is on are subjective measures of the vestibular system better than when the device is off? * Are the objective measures related to the subjective measures? Researchers will change the order of the device settings to ensure the changes aren't due to the order they are tested. Participants will: * Wear the Otolith Labs device while in a rotary chair at different settings for different tests. All of the rotary chair testing will take less than an hour. * Answer questions about how the rotary chair testing made them feel for each test. * Answer questions about their every-day susceptibility to motion sickness and about their vestibular migraine symptoms.

Official Title

VIBRANT-VM: Vestibular Investigation of Bone-conducted Resonant Analysis of Time-constants in Patients With Vestibular Migraines

Quick Facts

Study Start:2024-08-27
Study Completion:2025-11-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06540235

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.

Ages Eligible for Study:21 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Definite or probable vestibular migraine
  2. * Residing in the United States
  1. * Head injury (e.g. skull fracture, concussion) within the last six months
  2. * Neurodegenerative disorder
  3. * Recent use of specified medications
  4. * History of:
  5. * Vestibular neuritis / labyrinthitis
  6. * Vestibular schwannoma or acoustic neuroma
  7. * Radiographically unexplored unilateral or sudden sensorineural hearing loss
  8. * History of surgery to the skull base or head,
  9. * Surgery to the middle ear in the past 6 months,
  10. * Surgery to the inner ear (e.g. labyrinthectomy) at any time.
  11. * Eye surgery within the previous 3 months
  12. * Significant reported history of ear disease, intravenous ototoxic medications

Contacts and Locations

Principal Investigator

Didier Depireux, PhD
PRINCIPAL_INVESTIGATOR
Otolith Labs

Study Locations (Sites)

Dizzy and Vertigo Institute of Los Angeles
Beverly Hills, California, 90211
United States
Medical University of South Carolina
Charleston, South Carolina, 29425
United States

Collaborators and Investigators

Sponsor: Otolith Labs

  • Didier Depireux, PhD, PRINCIPAL_INVESTIGATOR, Otolith Labs

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 Registration Dates

Study Start Date2024-08-27
Study Completion Date2025-11-01

Study Record Updates

Study Start Date2024-08-27
Study Completion Date2025-11-01

Terms related to this study

Keywords Provided by Researchers

  • Vestibular Migraine
  • Central velocity storage
  • Vestibular condition
  • Migraine Associated Vertigo

Additional Relevant MeSH Terms

  • Vestibular Migraine