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Completed

NCT Number: NCT07297355

Four Ways to Be Dizzy: When Physiology Fails to Explain Disability Insights From the UVIS International Survey

The aim of this international study is to better understand how vestibular disorders affect daily life, including physical balance, vision and movement tolerance, emotional wellbeing, and cognitive functioning. Vestibular disorders are common but often difficult to diagnose because symptoms vary widely from one patient to another. To improve clinical care, we need large-scale information on the real-world experience of patients across different countries and clinical settings.

The UCLouvain Vertigo International Survey (UVIS) collects standardized information from adults with confirmed vestibular disorders, including questionnaires about dizziness-related handicap, emotional symptoms, and cognitive-vestibular complaints. Ear-nose-throat (ENT) specialists also provide routine clinical test results, such as caloric testing, vestibular evoked myogenic potentials (cVEMP and oVEMP), video head impulse tests (vHIT), and posturography. By combining these data, the study aims to identify different patient profiles and to examine how subjective symptoms relate to the physiological function of the vestibular system.

Participants take part during their routine clinical visit. They complete short questionnaires (on dizziness, anxiety, depression, cognitive symptoms, and daily functioning), and their ENT specialist encodes the results of the vestibular tests already performed as part of their usual care. No additional medical tests are required for the study.

By comparing data from several centers in Belgium, France, and the United States, this project seeks to provide a more complete picture of vestibular disorders worldwide and to support the development of better diagnostic tools and more personalized rehabilitation strategies.

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Cliniques universitaires Saint-Luc, Brussels, Belgium

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

For patients :

Inclusion criteria

  • Age between 18 and 90 years old.
  • Vestibular loss diagnosed by senior ENT doctors

Exclusion criteria

  • Previous neurological disorders (stroke, dementia, …)
  • Current medication interfering with the testing (reducing reaction time).
  • Visual difficulties interfering with the testing (Visual field reduction,…)
  • Age below 18 years old.

For healthy controls :

Inclusion criteria

  • Age between 18 and 90 years old.

Exclusion criteria

  • Previous neurological disorders (stroke, dementia, …)
  • Current medication interfering with the testing (reducing reaction time)
  • Visual difficulties interfering with the testing (Visual field reduction,…)
  • Vertigo or balance complains or an history of previous vestibular disorder.
  • Age below 18 years old.
  • Not being able to understand the consigns of the task.

Treatment and study plan

Primary outcomes

  1. Assessment of dizziness-related handicap

    Time frame: Through the entire study, approximately 36 months.

    DHI - Dizziness Handicap Inventory (25 items; physical, functional, emotional subscales). Scores 0-100. Higher scores = greater handicap.

  2. Assessment of emotional symptoms

    Time frame: Through the entire study, approximately 36 months.

    HADS - Hospital Anxiety and Depression Scale (14 items; Anxiety and Depression subscales). Scores 0-21 per subscale. Higher scores = more symptoms

  3. Assessment of cognitive-vestibular complaints

    Time frame: Through the entire study, approximately 36 months.

    NVI - Neuropsychological Vertigo Inventory (22 items assessing cognitive-vestibular symptoms: attention, memory, spatial orientation, visuospatial abilities). Higher scores = more complaints

Secondary outcomes

  1. Vestibular Physiological Function - canal paresis percentage

    Time frame: Through the entire study, approximately 36 months.

  2. Vestibular Physiological Function - cVEMP and oVEMP

    Time frame: Through the entire study, approximately 36 months.

  3. Vestibular Physiological Function - video Head Impulse Test

    Time frame: Through the entire study, approximately 36 months.

  4. Vestibular Physiological Function - Posturography

    Time frame: Through the entire study, approximately 36 months.

Sponsors and collaborators

Lead sponsor

Université Catholique de Louvain

Other

Registry information

Official study title

UVIS - UCLouvain Vertigo International Survey

Acronym: UVIS

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Dec 22, 2025
Registry last updated
Dec 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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