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Efficacy verification of unilateral spatial neglect treatment support system using a three-dimensional virtual reality space

Efficacy verification of unilateral spatial neglect treatment support system using a three-dimensional virtual reality space - Efficacy verification of unilateral spatial neglect treatment support system using a three-dimensional virtual reality space

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000020114
Enrollment
30
Registered
2015-12-22
Start date
2015-12-16
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 that is synchronized their hand of real in three-dimensional Virtual r
name that is pointed by therapist. The objects were installed on the desk. They took about 6 minutes. Patients were seated at a desk. They conducted visual scanning training on the screen. The screen
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 real
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

Waseda University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Scoring less than the cut off value in the line cancellation task. (2)No severe cognitive impairment (Mini-Mental State Examination, MMSE >15).

Exclusion criteria

Exclusion criteria: (1)unable to understand the task because of aphasia or other cognitive impairment. (2)unable to sit on a wheelchair. (3)Unable to recognize objects on a screen due to severely damaged eyesight. (4)unable to reach with the upper limb extremity because of restricted range of motion. (5)Inability to give informed consent form.

Design outcomes

Primary

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

Countries

Japan

Contacts

Public ContactHiroyasu Iwata

Waseda University Graduate School of Creative Science and Engineering, Department of Modern Mechanical Engineering

jubi@waseda.jp03-3203-4427

Outcome results

None listed

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