An Augmented Reality Based System for Neglect Detection, Assessment, and Rehabilitation
NCT ID: NCT04187131
Last Updated: 2025-07-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
10 participants
INTERVENTIONAL
2023-06-01
2027-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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augmented reality
augmented reality
The participants will be wearing an EEG cap and Augmented Reality headset (AR-based EEG-guided system) for 10 sessions with a licensed occupational therapist, provided in addition to usual rehabilitation care (either in inpatient rehabilitation or at home). These sessions will focus on activities of daily living that the participants want to practice. All sessions will last approximately 1 hour. These sessions will be scheduled around the existing therapy schedule to cause the least amount of interference with planned clinical activities.
Interventions
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augmented reality
The participants will be wearing an EEG cap and Augmented Reality headset (AR-based EEG-guided system) for 10 sessions with a licensed occupational therapist, provided in addition to usual rehabilitation care (either in inpatient rehabilitation or at home). These sessions will focus on activities of daily living that the participants want to practice. All sessions will last approximately 1 hour. These sessions will be scheduled around the existing therapy schedule to cause the least amount of interference with planned clinical activities.
Eligibility Criteria
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Inclusion Criteria
* acute stroke
* admitted to inpatient rehabilitation
* presence of neglect (Behavioral Inattention Test total score \<129, or scoring below pre-defined cutoff score in at least one of the six subtests)
* more than 10/% missed targets on the Augmented Reality Screening Test
* intact vibration (positive test on Vibration Sensation Test)
* intact auditory function (positive test on Auditory Sensation Test)
* English speaking
Exclusion Criteria
* current diagnosis of dementia, Parkinson's disease, multiple sclerosis, or space-occupying tumor
* metal in the head that causes interference with the EEG system
* self-report of previous positive photic stimulation test
18 Years
ALL
No
Sponsors
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Northeastern University
OTHER
NSF
UNKNOWN
University of Pittsburgh
OTHER
Responsible Party
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Murat Akcakaya
Assistant Professor, Electrical and Computer Engineering
Principal Investigators
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Murat Akcakaya, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Pittsburgh
Locations
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Northeastern University
Boston, Massachusetts, United States
University of Pittsburgh
Pittsburgh, Pennsylvania, United States
Countries
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Central Contacts
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Facility Contacts
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Murat Akcakaya, PhD
Role: primary
Other Identifiers
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1915083
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
STUDY19060390
Identifier Type: -
Identifier Source: org_study_id
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