The long-term goal of this research is to develop a new, non-invasive brain-computer interface (BCI) that will provide augmentative and alternative communication (AAC) capabilities to patients who have lost these capabilities due to severe motor impairments, such as completely locked-in syndrome (CLIS), amyotrophic lateral sclerosis (ALS), and severe cerebral palsy (CP). The proposed research project will work towards a long-term goal by developing a BCI based on brain imaging signals from high-density diffuse optical tomography (HDDOT). Some existing BCIs record electroencephalography (EEG) or electrocorticography (ECoG) signals from patients and then decode these signals into instructions for operating some element of the outside world, such as a cursor on a screen, a prosthetic limb, or a virtual keyboard. This functionality can enable communication. However, BCI generally has had limited success and capabilities in CLIS patients with EEG or has relied on invasive technology such as ECoG or intracortical recordings, which require surgical placement of electrodes on or beneath the brain surface. Although functional MRI (fMRI) has recently achieved great success with decoding items viewed or heard by subjects (e.g., distinguishing from among >100 viewed images), fMRI requires bulky, expensive equipment that cannot be employed for routine BCI for patients with severe motor- related communication deficits. In contrast, optical imaging approaches, such as near-infrared spectroscopy (NIRS), employ portable, wearable hardware. These optical systems are non-invasive and use non-ionizing, near-infrared light to create movies of blood oxygenation and therefore provide physiological information comparable to the fMRI signal. NIRS has recently been applied as an alternative to EEG BCI for decoding simple yes/no responses in CLIS patients. However, NIRS systems suffer from much-lower spatial resolution than fMRI, which renders NIRS unlikely to match the decoding capabilities of fMRI. High-density diffuse optical tomography (HDDOT) combines the lightweight, low-cost equipment benefits of EEG and NIRS with higher spatial resolution closer to that of fMRI at the brain surface. Recent advances in HDDOT systems have enabled average spatial localization errors <5 mm and spatial resolution <17-20 mm (substantially better than NIRS). Studies have demonstrated detailed maps of both visual and language tasks. These properties make HDDOT an ideal candidate tool for decoding brain function. The fellowship training will provide a strong foundation in optical neuroimaging methods, machine learning, and brain-computer interface. These experiences will prepare the applicant exceptionally well for a career in biomedical engineering research and for developing technology that will improve these patients? quality of life.

Public Health Relevance

This project will develop decoding methods and evaluate their feasibility for using a high- performance optical brain scanner to identify and distinguish between imaging tasks in human subjects. The long-term goal of this research is to enable locked-in patients to communicate with others using augmented communication facilitated by a portable brain-scanning device, and a computer that decodes their brain signals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31NS110261-02
Application #
10078847
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Kukke, Sahana Nalini
Project Start
2020-01-01
Project End
2021-12-31
Budget Start
2021-01-01
Budget End
2021-12-31
Support Year
2
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Washington University
Department
Type
Computer Center
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130