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Effects of immersive virtual reality mobility slit training on patients with unilateral spatial neglect -A Randomized Controlled Trial-

Effects of immersive virtual reality mobility slit training on patients with unilateral spatial neglect -A Randomized Controlled Trial- - Effects of immersive virtual reality mobility slit training on patients with unilateral spatial neglect -A Randomized Controlled Trial-

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055790
Enrollment
54
Registered
2024-10-10
Start date
2024-11-01
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

Unilateral spatial neglect in stroke patients.

Interventions

name of far space in three-dimensional Virtual reality space with HMD. Second, they touch the objects of near space with one hand hat is synchronized their hand of real in three-dimensional Virtual re
name that is pointed by therapist. The objects were installed on the screen. They took about 6 minutes. Patients were attached a Head-mounted display (HMD) and presented three-dimensional Virtual re
name of far space in three-dimensional Virtual reality space with HMD. At this time patients attention is inducted to neglect side of a object. They took about 13 minutes.

Sponsors

Wasada University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Imaging findings show foci in the right cerebral hemisphere. (2)Patients who have neglected symptoms in the linear bisection test. (3)Patients who have a reduced score on the Catherine Bergego Scale (hereinafter referred to as CBS) observation method. (4)Patients who have had the disease for more than 1 month since the onset.

Exclusion criteria

Exclusion criteria: (1)Patients with homonymous hemianopia (2)Those with difficulty in evaluation due to significant vision loss. (3)Patients with complaints of mood discomfort due to VR sickness (4)Those who could not give consent for the study. (5)Patients who have difficulty in following the subject due to oculomotor paralysis

Design outcomes

Primary

MeasureTime frame
Line cancellation, Line bisection, star cancellation and letter cancellation task. Time of assessment:immediately before the in tervention and immediately after the intervention

Countries

Japan

Contacts

Public ContactHiroyasu Iwata

Waseda University Faculty science and engineering

jubi@waseda.jp03-3203-4427

Outcome results

None listed

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