1 Department of Biomedical Engineering,
2
3 Department of Neurology,
Email- andrew.cornwell@cas
Neuroprosthetics
employing Functional Electrical Stimulation (FES) have grown to become an
accepted therapy and treatment for certain individuals with severe neurological
impairment. Several examples have shown
that this technology can restore effective function in the upper and lower extremity. However, to expand the populations of these
individuals who may be able to benefit from this technology, improved ways for
the subject to command FES-generated movements are needed. Current technology focuses on using retained
motor function, through movement of unaffected joints or EMG recordings from
nonparalyzed muscle activity. This
limits application to individuals with some remaining function and excludes
those with severe stroke, amyotrophic lateral sclerosis, or high-level spinal
cord injury. Therefore, much recent effort has been focused on recording
subdural electroencephalographic signals, called electrocorticogram (ECoG), as
a command sourc
2.
METHODS
2.1 Motion Data Collection
The position of the arm is
determined using the Fastrak electromagnetic motion tracking system by
Polhemus, Inc. Three sensors are used to
determine the position of the arm relative to the torso. The first sensor is securely taped to the
sternum, the second is strapped to the dorsal aspect of the upper arm close to
the elbow, and the third sensor is strapped to the forearm over the dorsal
aspect of the wrist. The two arm sensors
are held in place by tight Velcro straps.
Using a stylus, bony landmarks are identified relative to the
appropriate sensors according to Table I.

Features of the arm motion
are extracted from these bony landmarks, including endpoint position, velocity,
acceleration, and joint angles. The
joint angles are determined using the protocol determined by the International
Shoulder Group [1].
Each subject undertook a
series of arm movements that included center-out tasks,
reaching movements and simulated activities related to feeding.
Calibration of the workspace
to compensate for electromagnetic distortion was accomplished using a
polynomial regression, similar to [2].
Known points in the workspace are marked using an orthogonal 3-D 5 x 5 x
3 grid, and then using the stylus to mark the same positions as measured by the
Fastrak. The error at each point is
calculated, and a polynomial regression is performed in the x-, y-, and
z-directions to predict and account for the errors between the measured points.
2.2. ECoG Data Collection
Electroencephalographic signals are recorded at the
Epilepsy Monitoring Unit at the Cleveland Clinic Foundation in
2.3. Signal Processing
The motion data is used as recorded, after
compensating for electromagnetic distortion.
These data, recorded at about 12Hz, are resampled to 200Hz in order to
match the sampling frequency of the recorded ECoG signal.

Several features of the ECoG data were examined. First, a spatial Laplacian filter was applied
to each electrode of interest [3], and then each of the following techniques
was applied to every channel, and the result is used as the input to the ANN: Windowed Variance is the variance of the
signal over the preceding second. Median Power is the frequency at which half
of the spectral power is above, and one half below, calculated over the
preceding second. Moving estimates of
power in frequency bands known to have correlation to movement were calculated. Finally, a 4th order autoregressive model of
the data was fit to each channel. The
model uses a “forgetting factor” algorithm, and thus the model parameters
contain dynamic spectral information for a preceding period of time, determined
by the forgetting factor coefficient (λ).
2.4. Artificial Neural
Networks
A time-delayed, feed-forward, backpropagating
artificial neural network was implemented in the MATLAB environment. The network used linear neurons as input and
output layers, and contained one hidden layer of sigmoidal neurons. Inputs to the network were the results of one
of the signal processing techniques described abov
3.
RESULTS

In figure 1, the accuracy of the calibration of the motion tracking system is demonstrated. During the calibration, a 5 x 5 x 3 grid of points is gathered; only one of the five X-Z planes is shown for clarity. The straight dark lines indicate the exact measured positions. Points marked by a solid dot represent the pre-calibration points calculated by the Fastrak system, and points marked by an X represent the same points after the error correction has been applied. Note the reduction in systematic error between the original, pre-calibration points and the final, calibrated points. Repeated calibrations at the conclusion of the trials demonstrate that the single calibration before gathering data is sufficient. Mean Squared Error is typically reduced to less than 10% of the original, and is around 0.5cm. Figure 2 shows the results of network training on a single reaching type movement. The network input was the power in the 8-12 Hz range, which has been shown to be highly correlated to movement [4],[5]. The output used for training and prediction was 3-D endpoint location. These data are the training set only, which show the high correlation that can be discerned by the ANN algorithm.
The predictive
capability of the ANN is shown in Figure 3.
Here, the network was presented with a series of novel, pre-processed
ECoG data as inputs and a binary target signal, where a target value of “1”
signified motion, and a “0” signified rest.
The network accurately predicted the presence of nonstereotypical
movement with a variety of speeds and directions.
4. DISCUSSION AND CONCLUSIONS
The clinical
environment is not conducive to recording the electromagnetic signals used by
the Fastrak system. However, through the
use of careful calibration of a small workspace, the distortion present in this
setting can be overcom
Figure 1
demonstrates the accuracy of the polynomial approach in this case, where the
distortion is of low spatial frequency relative to the workspace volum
In Figure 2, the
correlation between the recorded endpoint position and that predicted by the
ANN is evident. Although significant
noise around the mean is noticeable, this high-frequency component is not
useful information, and can be filtered to produce a smooth correlation. These data represent the first step toward
prediction of movement features from ECoG signals. In this case only a single feature, the power
in the 8-12 Hz μ frequency band, is used as input. It is anticipated that several features of
the ECoG signal will be necessary for improving generalization, and ultimately
for prediction.
A simple
prediction task is represented in Figure 3.
Here, the network is able to predict the presence of movement. The movements shown are not repeated,
averaged, or cue-based.
Although
population vectors from single unit recordings have been shown to be excellent
predictors of endpoint location [6], it is increasingly evident that local
field potentials from cortical or scalp surface recordings can provide
additional useful information [7], in addition to providing a useful bridging
step in the development of cortically controlled FES systems.
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[2] C. G. Meskers, H. Fraterman, F. C. van der Helm, H. M. Vermeulen, and P. M. Rozing, "Calibration of the "Flock of Birds" electromagnetic tracking device and its application in shoulder motion studies," Journal of Biomechanics, vol. 32, pp. 629-33, 1999.
[3] F. Babiloni, F. Cincotti, L. Lazzarini, J. Millan, J. Mourino, M. Varsta, J. Heikkonen, L. Bianchi, and M. G. Marciani, "Linear classification of low-resolution EEG patterns produced by imagined hand movements," IEEE Transactions on Rehabilitation Engineering, vol. 8, pp. 186-8, 2000.
[4] C. Toro, C. Cox, G. Friehs, C. Ojakangas, R. Maxwell, J. R. Gates, R. J. Gumnit, and T. J. Ebner, "8-12 Hz rhythmic oscillations in human motor cortex during two-dimensional arm movements: evidence for representation of kinematic parameters," Electroencephalography & Clinical Neurophysiology, vol. 93, pp. 390-403, 1994.
[5] J. R. Wolpaw and D. J. McFarland, "Multichannel EEG-based brain-computer communication," Electroencephalography & Clinical Neurophysiology, vol. 90, pp. 444-9, 1994.
[6] D. Taylor and
[7] J. R. Wolpaw, N. Birbaumer, D. J. McFarland, G. Pfurtscheller, and T. M. Vaughan, "Brain-computer interfaces for communication and control.," Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology, vol. 113, pp. 767-91, 2002.
Acknowledgements
Funding
for this project is provided by Case’s IGERT fellowship in Neuromechanics, NSF
IGERT DGE 9972747