The study comparing the conventional test and using the immersive VR method

Phase 1

Recruiting

• Conditions: stroke (cerebral infarction, cerebral hemorrhage); left unilateral spatial neglect

• Registration Number: JPRN-jRCTs032200451
• Lead Sponsor: Wada Naoki

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-03-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

patient group
1) with ages ranging from 40 to 79.
2) male and female.
3) presence of a first-time right hemisphere stroke (cerebral infarction or cerebral hemorrhage).
4) even if the patients have aphasia, they can understand the instructions and perform the tests.
5) more than 2 weeks after onset and be in a stable condition.
6) can sit independently on chair or in wheelchair.
7) signed informed patients or family consent.

healthy group
1) with ages ranging from 40 to 79.
2) male and female.
3) signed informed subjects or family consent.

Exclusion Criteria

patient group
1) a history of major neurological disorders other than stroke.
2) a history of major psychiatric disorders.
3) with head injury.
4) with disturbance of consciousness.
5) with cognitive disorders (the score of Mini-Mental State Examination under 23).
6) presence of visual impairment (e.g. visual field deficit, damage to the optic radiation and the occipital lobe).
7) judged to be unsuitable to the assessment by doctors in the team. The study was approved by the local ethics committee at the hospital, and written informed consent was obtained from all subjects.

healthy group
1) a history of major neurological disorders other than stroke.
2) a history of major psychiatric disorders.
3) with head injury.
4) with disturbance of consciousness.
5) with cognitive disorders (the score of Mini-Mental State Examination under 23).
6) presence of visual impairment (e.g. visual field deficit, damage to the optic radiation and the occipital lobe).
7) judged to be unsuitable to the assessment by doctors in the team. The study was approved by the local ethics committee at the hospital, and written informed consent was obtained from all subjects.

Study & Design

• Study Type: Interventional
• Study Design: Not specified