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Development of an Exercise Evaluation Program Using Virtual Reality Devices for Unilateral Spatial Neglect

Development of an Exercise Evaluation Program Using Virtual Reality Devices for Unilateral Spatial Neglect - Development of an Exercise Evaluation Program Using Virtual Reality Devices for Unilateral Spatial Neglect

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060934
Enrollment
30
Registered
2026-03-16
Start date
2026-03-17
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

Healthy individual

Interventions

Participants will perform all three sets of VR programs in the assigned order. Each session lasts approximately 10 minutes. A washout period of at least 48 hours is observed between sessions. The inte

Sponsors

Kagoshima University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Individuals with no history of stroke or higher brain dysfunction. Individuals who have provided written consent to participate in the study. Individuals aged 20 to 80 years old on the date consent is obtained (gender is not a factor). Individuals capable of understanding and following the instructions presented within the VR environment by the researcher.

Exclusion criteria

Exclusion criteria: Individuals with a history of stroke. Individuals diagnosed with unilateral spatial neglect. Individuals with cognitive impairments that make it difficult to understand the study instructions. Individuals with upper limb paralysis, limited joint range of motion, or ataxia that would interfere with the performance of the reaching task. Individuals with severe visual impairment (uncorrectable) that affects task performance. Individuals who have previously experienced severe motion sickness or intense discomfort from VR use. Individuals who experienced intense discomfort during the trial VR session. Any other individuals deemed unsuitable for the study by the principal investigator.

Design outcomes

Primary

MeasureTime frame
The angle of afterimage immediately following the completion of 30 prism adaptation trials, as measured using the newly developed method and the conventional method

Countries

Japan

Contacts

Public ContactMakoto Ueno

Kagoshima University Rehabilitation Medicine

k0720622@kadai.jp099-275-5339

Outcome results

None listed

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