SBIR-STTR Award

Development of Neurocognitive Eye Tracking for Rapid Screening of Mild Cognitive Impairment
Award last edited on: 1/22/20

Sponsored Program
SBIR
Awarding Agency
NIH : NIA
Total Award Amount
$305,604
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Dorion Bryce Liston

Company Information

neuroFit Inc

1398 West El Camino Real Suite E
Mountain View, CA 94040
   (650) 300-2499
   N/A
   www.neurofit.tech
Location: Single
Congr. District: 18
County: Santa Clara

Phase I

Contract Number: 1R43AG066427-01
Start Date: 9/30/19    Completed: 8/31/20
Phase I year
2019
Phase I Amount
$305,604
Alzheimer’s Disease (AD) affects an estimated 5.8 million adults in the U.S. By 2030 this number is expected to increase almost 45% to 8.4 million and without new treatment or interventions, by 2050 there will be more than 13.8 million seniors living with Alzheimer’s dementia in the U.S. (Alzheimer's Association, 2019). AD is associated with a spectrum of neurocognitive signs and symptoms that lead to significant morbidity and mortality, and the lack of readily-available screening for neurocognitive decline has led to a situation where most dementia cases are detected and diagnosed when the disease becomes overt, adding risk to patients in early stages of degenerative disease and burdening the healthcare system with additional costs. Our Phase I SBIR project will develop novel oculometric (i.e., eye-movement-based) technologies for functional assessment of neural circuits, useful as a monitoring biomarker during healthy aging and to the monitor progression of healthy aging, mild cognitive impairment (MCI) and AD. The clinical significance and market need for improved assessment of MCI and AD is established by three main points. First, and most importantly, a large number of seniors are living with undetected dementia (Sternberg et al., 2000) and only sixteen percent of seniors undergo cognitive screening on a yearly basis (Alzheimer's Association, 2019) indicating a need for new techniques, methods, and technologies. Second, progress in development of effective drugs for AD is hindered by outdated, subjective outcome measures (Mehta et al., 2017). Third, monitoring biomarkers are needed to assess effects of lifestyle interventions (Kivipelto et al., 2018) and other modifiable risk factors for dementia (Livingston et al., 2017). Together, these gaps, limitations, and encouraging possibilities necessitate the development of novel biomarkers of central nervous system (CNS) function. Our team will develop a battery of eye-movement-based tests tuned to the specific cognitive impairments that arise in MCI and AD, to be implemented using the neuroFit ONE oculometric R&D platform. We will also use neuroFit ONE to prototype a novel computational architecture for eye-tracking appropriate for use with diverse patient populations, suitable for incorporation into consumer electronic devices. Our goal is to develop a suite of oculometric tools suitable for medical and consumer use: high-sensitivity medical devices for use in the clinic and a consumer-grade solution for distribution in electronic devices (e.g., virtual reality headsets).

Public Health Relevance Statement:
Project Narrative Alzheimer’s Disease affects an estimated 5.8 million adults in the U.S., its progression marked by decline in several cognitive domains. The lack of readily-available screening for neurocognitive decline has led to a situation where most dementia cases are detected and diagnosed when the disease becomes overt, adding risk to patients in early stages of degenerative disease and burdening the healthcare system with additional costs (Alzhimer’s Association, 2018). Our project will develop a battery of eye-movement-based tests tuned to the specific cognitive impairments that arise in Mild Cognitive Impairment and Alzheimer’s Disease and Related Dementias. This project will deliver robust oculometric technologies developed and tested using populations of seniors, suitable for later application of oculometric technologies in consumer devices.

Project Terms:
Adult; adverse outcome; Affect; Age; age effect; Alzheimer's Disease; Alzheimer's disease related dementia; Alzheimer's disease risk; American; Architecture; Attention; base; Biological Markers; Brain; burden of illness; Catalogs; Clinic; Clinical; clinical practice; Clinical Trials; clinically significant; Cognitive; Collaborations; Collection; Consumption; cost; Data; Data Set; Degenerative Disorder; Dementia; dementia risk; design; Development; Devices; Diagnosis; Disease; Disease Progression; Effectiveness; Electronics; executive function; Eye; Eye Movements; Face; falls; Feasibility Studies; Future; Geriatrics; Goals; Healthcare Systems; healthy aging; Hospitalization; Image; Impaired cognition; Impairment; improved; Individual; Intervention; Lead; lifestyle intervention; Measures; Medical; Medical Device; Memory; Methods; mild cognitive impairment; modifiable risk; Monitor; Morbidity - disease rate; mortality; Nervous System Physiology; neural circuit; Neuraxis; Neurocognition; Neurocognitive; Neurocognitive Deficit; neuropathology; Neuropsychology; new technology; novel; novel marker; oculomotor; Outcome Measure; Pathway interactions; patient population; Patients; Perception; Pharmaceutical Preparations; Phase; Population; Population Heterogeneity; processing speed; product development; prototype; Psychometrics; Race; research and development; Research Personnel; Risk; Risk Management; Sampling; Scientist; screening; Severities; Signs and Symptoms; Small Business Innovation Research Grant; Standardization; statistics; Surveys; Techniques; Technology; Testing; Time; tool; Training; vehicular accident; virtual reality; visual motor; Visuospat

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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