Menu
Recruiting NCT06575946

Relationship Between Degree of Hypofunction and Vestibular Tests in Patients With Vestibular Hypofunction

No phase Interventional Videonystagmography Vestibular Assessment

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Vestibular Hypofunction Group.
Who it may be relevant to
Registry conditions: Videonystagmography, Vestibular Assessment. Basic parameters: 12 years — 85 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Investigation of the Relationship Between the Degree of Hypofunction and Vestibular Tests in Patients With Vestibular Hypofunction

Overview

Patients with complaints of dizziness and balance problems will be included in the study. Inclusion criteria for the study are; being between the ages of 12-85, having a diagnosis of peripheral vestibular hypofunction. Exclusion criteria from the study are; not being able to communicate, having a diagnosis of central vestibulopathy and having mental disorders. Demographic information form, vestibular tests, balance tests will be used in the evaluation. The demographic information form includes demographic information (name, surname, gender, smoking, alcohol use, etc.) and clinical conditions (past illnesses and/or surgeries, medications used, whether there is a history of falls, if any, frequency, whether they are afraid of heights and uncomfortable in the dark, etc.). The patients will be diagnosed with videonystagmography (VNG) after the decision of the ENT physician, and the degree of hypofunction will be recorded. Vestibular and balance tests will be applied to the patients in a clinical setting. At the end of the study, it will be examined whether there is a relationship between the degree of vestibular hypofunction and the vestibular tests applied in the clinic.

Interventions

  • Diagnostic test Vestibular Hypofunction Group
    Demographic information form, vestibular tests, balance tests will be used in the evaluation. The demographic information form includes demographic information (name, surname, gender, smoking, alcohol use, etc.) and clinical conditions (past illnesses and/or surgeries, medications used, whether there is a history of falls, if any, frequency, whether they are afraid of heights and uncomfortable in the dark, etc.). The patients will be diagnosed with videonystagmography (VNG) after the decision of

Primary outcome measures

  • Demographic information and data collection form [Time frame: through study completion, average 2 months]
  • Unterberger Test [Time frame: through study completion, average 2 months]
  • Dynamic Visual Acuity [Time frame: through study completion, average 2 months]
  • Head Thrust Test [Time frame: through study completion, average 2 months]
  • Timed Balance Tests [Time frame: through study completion, average 2 months]
  • Dizziness Handicap Inventory (DHI) [Time frame: through study completion, average 2 months]
  • Tampa Kinesiophobia Scale (TKS) [Time frame: through study completion, average 2 months]
  • Static Posture Assessment with ICS [Time frame: through study completion, average 2 months]
  • Videonystagmography (VNG) [Time frame: through study completion, average 2 months]

Eligibility criteria

Inclusion criteria

  • Being between 12-85 years old
  • Having peripheral vestibular hypofunction
  • Having good communication skills and participating in the work willingly

Exclusion criteria

  • Having wavy vertigo
  • Having mental retardation
  • Failure to communicate
  • Severely limited mobility
  • Having acute Meniere's disease
  • Having a neurological problem

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

Turkey (Türkiye) · 1 center
  • Güneşli Erdem Hospital — Bağcılar

Identifiers

NCT: NCT06575946 · VNG-VESTIBULAR TESTS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗