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Creating a visual stimulator

Creating a visual stimulator using a head-mounted display (HMD) - Creating a visual stimulator using HMD

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000049246
Enrollment
30
Registered
2022-10-18
Start date
2022-10-18
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

Vestibular disorder

Interventions

The participants will wear a head-mounted display (HMD). Pseudo-linear and pseudo-rotational visual stimuli are added on the HMD, and the visibility is verified by a questionnaire method. The test t

Sponsors

St. Marianna University School of Medicine
Lead Sponsor
Nagashima Medical Instruments.Co.,Ltd.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy subjects who do not have an equilibrium disorder and who have given their free and voluntary written consent to participate in this study, after having demonstrated sufficient understanding of the study after the explanation of the study.

Exclusion criteria

Exclusion criteria: Cases in which consent was not obtained, and other cases in which participation in the study was deemed impossible due to medical conditions or physical condition.

Design outcomes

Primary

MeasureTime frame
Using the created HMD, perform pseudo-linear and pseudo-rotational visual stimulation on the subject. Subjects will be asked to complete a questionnaire immediately following the study. Evaluate the validity of the stimuli by asking the participants to describe whether they feel as if they moved reality in a straight line when they experienced the pseudo-linear visual stimuli, and whether they feel as if they rotated reality when they experienced the pseudo-rotational visual stimuli ("felt", "felt a little", or "did not feel").

Secondary

MeasureTime frame
Using the created HMD, perform pseudo-linear and pseudo-rotational visual stimulation on the subject. Subjects will be asked to complete a questionnaire immediately following the study. The participants will be asked to describe whether nausea or other symptoms appeared during the test ("felt", "felt a little", or "did not feel") to evaluate safety.

Countries

Japan

Contacts

Public ContactYusuke Ito

St. Marianna University School of Medicine Otorhinolaryngology

yusuke.ito@marianna-u.ac.jp044-977-8111(ext.3261)

Outcome results

None listed

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