Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04187131

An Augmented Reality Based System for Neglect Detection, Assessment, and Rehabilitation

Led by University of Pittsburgh · Updated on 2025-07-11

10

Participants Needed

2

Research Sites

226 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

N

Northeastern University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this phase is to examine the feasibility and acceptability of the Augmented Reality (AR)-based and electroencephalography (EEG)-based neglect detection and rehabilitation tool.

CONDITIONS

Official Title

An Augmented Reality Based System for Neglect Detection, Assessment, and Rehabilitation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 18 and older
  • Acute stroke
  • Admitted to inpatient rehabilitation
  • Presence of neglect indicated by Behavioral Inattention Test total score less than 129 or below cutoff in at least one of six subtests
  • More than 10% missed targets on the Augmented Reality Screening Test
  • Intact vibration sensation (positive Vibration Sensation Test)
  • Intact auditory function (positive Auditory Sensation Test)
  • English speaking
Not Eligible

You will not qualify if you...

  • Inability to follow one-step directions at least 80% of the time
  • Current diagnosis of dementia, Parkinson's disease, multiple sclerosis, or space-occupying tumor
  • Metal in the head that interferes with EEG system
  • Previous positive photic stimulation test by self-report

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Northeastern University

Boston, Massachusetts, United States, 02115

Not Yet Recruiting

2

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15260

Actively Recruiting

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Research Team

M

Murat Akcakaya, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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