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Mixed-Reality Visual Attention Task for Neglect Diagnosis and Rehabilitation (Neglex01)

M

Markey Olson

Status

Not yet enrolling

Conditions

Neglect, Hemispatial
Neglect, Hemisensory
Neglect, Sensory

Treatments

Device: VR Neglect Training

Study type

Interventional

Funder types

Other

Identifiers

NCT07227844
26-500-131-30-06

Details and patient eligibility

About

Neglect, a common and disabling neurological deficit post-CNS injury, profoundly hinders recovery and escalates healthcare costs. Current diagnostic tools are often insensitive or impractical, and while therapies exist, a significant research gap remains. Traditional methods, including standardized scales and paper-pencil tests, lack precision; even advanced video oculography is limited by cost and accessibility. Rehabilitative approaches like visual scanning and prism adaptation offer some benefit, but more effective solutions are needed. This project utilizes a non-invasive neuromodulatory training approach via a mixed-reality visual attention task delivered through a virtual reality headset. This system aims to improve both neglect diagnosis and personalized therapeutic intervention. The study will assess the headset's safety and practicality, its capacity to detect and lateralize neglect, and its long-term effect on improving attention to the neglected field. By measuring reaction times to visual stimuli within the VR environment, the research seeks to develop a more accessible and impactful tool for both assessing and treating neglect, potentially enabling self-directed therapy and enhancing patient outcomes.

Enrollment

5 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The study will involve patients over the age of 18 who have been diagnosed with a neurological injury that includes: ischemic stroke, hemorrhagic stroke, tumor, or trauma.
  • Neurological injury that localizes to only one side of the brain
  • At least one hand that retains dexterity enough to use a controller to extinguish the visual stimulus.
  • Cognitive ability to understand simple instructions on how to use the device
  • Visual fields intact

Exclusion criteria

  • Bilateral symptomatic injury
  • Inability to consent or to comply with study
  • Blindness or severe visual deficits other than neglect

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

5 participants in 1 patient group

Treatment
Experimental group
Treatment:
Device: VR Neglect Training

Trial contacts and locations

1

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Central trial contact

Markey Olson, PhD

Data sourced from clinicaltrials.gov

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