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Computerized Rotational Head Impulse Test-Vertical (crHIT-vertical)

Not Applicable
Conditions
Vestibular Function Tests
Registration Number
NCT04087044
Lead Sponsor
Neurolign
Brief Summary

The purpose of this research study is to test whether a Computerized Rotational Head Impulse Test-Vertical (crHIT-vertical) is able to reliably evaluate the vertical semicircular canals in patients with vestibular dysfunctions.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
186
Inclusion Criteria
  • Subjects must be willing to tolerate the placement of a set of goggles on their face

  • Controls:

    1. no history of dizziness or imbalance
    2. normal responses on rotational chair testing
  • Patients: persons clinically diagnosed with vestibular disorders

Exclusion Criteria
  • Pregnancy
  • Neurodegenerative diseases

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Sensitivity and specificity of crHIT-vertical9 months

How many participants are correctly identified as either having a vestibular dysfunction or being healthy controls

Secondary Outcome Measures
NameTimeMethod
Subject discomfort - symptoms9 months

Number of subjects indicating motion sickness symptoms during the crHIT test. If motion sickness is present subjects are asked to rate the symptoms of motion sickness and severity on scale 1 to 5, where 1 is minimum and 5 is severe.

Subject discomfort - test apparatus9 months

Subjects rate the comfort of chair, head rest and goggle on scale 1 to 5, where 1 is very uncomfortable and 5 very comfortable.

Trial Locations

Locations (3)

University of Miami

πŸ‡ΊπŸ‡Έ

Miami, Florida, United States

Mayo Clinic Rochester

πŸ‡ΊπŸ‡Έ

Rochester, Minnesota, United States

University of Pittsburgh

πŸ‡ΊπŸ‡Έ

Pittsburgh, Pennsylvania, United States

University of Miami
πŸ‡ΊπŸ‡ΈMiami, Florida, United States

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