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A Study on the Diagnostic Accuracy of a Dizziness Testing Device Using VR Goggles

A Study on the Diagnostic Accuracy of a Dizziness Testing Device Using VR Goggles - A Study on the Diagnostic Accuracy of a Dizziness Testing Device Using VR Goggles

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000059434
Enrollment
120
Registered
2025-10-17
Start date
2025-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dizziness,Vertigo

Interventions

Optokinetic stimuli (alternating black and white stripes presented in front of the eyes in a sitting position are accelerated at 1 degree/sec2 to the right or left and the participants are instructed

Sponsors

University of Toyama
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Non-dizziness subject group: adult subjects aged 18 years and over with no history of ear disease (otitis media, perforated tympanic membrane, etc.), hearing loss, or dizziness/imbalance disorder. Dizziness patient group: Dizziness patients who attended the Advanced Vertigo Centre of Toyama University Hospital with a chief complaint of vertigo or dizziness and were diagnosed with peripheral vestibular disorder or central disequilibrium disorder (or suspected).

Exclusion criteria

Exclusion criteria: 1 Persons with complications that may seriously interfere with the conduct of the study (interstitial pneumonia, pulmonary fibrosis, severe emphysema, uncontrolled diabetes or hypertension, history of myocardial infarction within 3 months, uncontrolled angina pectoris or irregular heartbeat, etc., heart failure, liver failure, renal failure, peptic ulcer, etc.) 2 Women who are pregnant, lactating or intend to become pregnant during the study period. 3 Those with a history of hospital visits or medication for psychiatric disorders. 4 Any other person who is judged by the principal investigator to be inappropriate as a subject for this study, including a.Persons who are judged to have poor comprehension of the instructions and requests of the researchers b.Persons who are judged to be uncooperative in responding to the instructions and requests of the researchers c.Others

Design outcomes

Primary

MeasureTime frame
(i) Optokinetic nystagmus test: maximum slow phase velocity of nystagmus during optokinetic stimulation. (ii) Caloric test: maximum slow phase velocity of nystagmus and rate of fixation suppression during four stimulation conditions (right ear cold stimulation, right ear warm stimulation, left ear cold stimulation and left ear warm stimulation).

Countries

Japan

Contacts

Public ContactHiromasa Takakura

Toyama University Hospital Department of Otolrhinolaryngology, Head and Neck surgery

hiromasa@med.u-toyama.ac.jp076-434-2281

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026