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VR System for Cross-modal Rehabilitation of Hemianopia

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Completed

Conditions

Hemianopsia, Homonymous
Hemianopia, Homonymous

Treatments

Device: Cross-model Visual Auditory Rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT04230486
IRB00061542

Details and patient eligibility

About

The purpose of this research study is to investigate the effectiveness of a new rehabilitation for visual hemianopia. The study team believes a cross-modal rehabilitation technique delivered by a virtual reality system can help restore the visual field for subjects with homonymous hemianopia.

Full description

The study tests a novel rehabilitation system, translated from promising cross-modal rehabilitation animal research, that is the first treatment capable of restoring the visual field for hemianopia patients. This noninvasive technique uses a virtual reality device to deliver visual and auditory stimulus. The goals of this study are to obtain proof of concept and procure rehabilitation data to support the development of this novel rehabilitation treatment.

Enrollment

6 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult volunteers diagnosed with homonymous visual hemianopia / hemianopsia (ages 18-99)

Exclusion criteria

  • Volunteers who are unable to complete the study tasks or understand instructions
  • Subjects that are not able to provide written consent or verbal assent
  • Subjects who are not available to complete all rehabilitation sessions

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

6 participants in 1 patient group

Experimental Group Virtual Reality (VR) Treatment
Experimental group
Description:
Visual Auditory Virtual Reality rehabilitation for visual hemianopia
Treatment:
Device: Cross-model Visual Auditory Rehabilitation

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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