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Mixed-Reality Visual Attention Task for Neglect Diagnosis and Rehabilitation

Pilot Study of a Mixed-Reality Visual Attention Task for Neglect Diagnosis and Rehabilitation

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07227844
Acronym
Neglex01
Enrollment
5
Registered
2025-11-13
Start date
2025-12-31
Completion date
2026-12-31
Last updated
2025-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neglect, Hemisensory, Neglect, Hemispatial, Neglect, Sensory

Keywords

neglect

Brief summary

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.

Interventions

VR Neglect Training

Sponsors

Markey Olson
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Improvement in Neglect6 monthsMeasured as improvement in percentage of lines detected at each location in the VR app

Secondary

MeasureTime frameDescription
Feasibility/Usage, sessions6 monthsNumber of sessions completed by each participant
Feasibility/Usage, time6 monthsTotal time spent using the device

Countries

United States

Contacts

Primary ContactMarkey Olson, PhD
neuromodulationresearch@commonspirit.org602-406-5944

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026