Title | A P300-based brain-computer interface for people with amyotrophic lateral sclerosis. |
Publication Type | Journal Article |
Year of Publication | 2008 |
Authors | Nijboer, F, Sellers, EW, Mellinger, J, Jordan, MA, Matuz, T, Furdea, A, Halder, S, Mochty, U, Krusienski, DJ, Vaughan, TM, Wolpaw, J, Birbaumer, N, Kübler, A |
Journal | Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology |
Volume | 119 |
Pagination | 1909–1916 |
Date Published | 08/2008 |
ISSN | 1388-2457 |
Keywords | Amyotrophic Lateral Sclerosis, brain-computer interface, electroencephalogram, event-related potentials, P300, Rehabilitation |
Abstract | OBJECTIVE:
The current study evaluates the efficacy of a P300-based brain-computer interface (BCI) communication device for individuals with advanced ALS.
METHODS:
Participants attended to one cell of a N x N matrix while the N rows and N columns flashed randomly. Each cell of the matrix contained one character. Every flash of an attended character served as a rare event in an oddball sequence and elicited a P300 response. Classification coefficients derived using a stepwise linear discriminant function were applied to the data after each set of flashes. The character receiving the highest discriminant score was presented as feedback.
RESULTS:
In Phase I, six participants used a 6 x 6 matrix on 12 separate days with a mean rate of 1.2 selections/min and mean online and offline accuracies of 62% and 82%, respectively. In Phase II, four participants used either a 6 x 6 or a 7 x 7 matrix to produce novel and spontaneous statements with a mean online rate of 2.1 selections/min and online accuracy of 79%. The amplitude and latency of the P300 remained stable over 40 weeks.
CONCLUSIONS:
Participants could communicate with the P300-based BCI and performance was stable over many months.
SIGNIFICANCE:
BCIs could provide an alternative communication and control technology in the daily lives of people severely disabled by ALS.
|
URL | http://www.ncbi.nlm.nih.gov/pubmed/18571984 |
DOI | 10.1016/j.clinph.2008.03.034 |