Page 143 - Handbook of Biomechatronics
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140                                                     Domen Novak


          be as low as 0.1Hz (Novak and Riener, 2015). Most of the EEG paradigms
          can then also be applied to ECoG. However, due to its higher SNR, it is
          possible to use additional signal analysis paradigms that achieve much more
          accurate estimation of the user’s desired motions. While EEG-based motor
          imagery can only identify broad classes such as “move left arm” vs “move
          right arm,” ECoG and intracortical electrodes allow “movement decoding”:
          reconstruction of the detailed movement trajectory (actual or desired) from
          the brain signal. Similarly to motor imagery analysis, this process usually
          begins by extracting frequency features from a PSD estimated over a sliding
          window. These features are transformed into an estimate of the desired
          motion trajectory by means of linear regression (Chao et al., 2010) or more
          advanced methods such as Kalman filters (Hochberg et al., 2012) and then
          used as direct inputs to a biomechatronic device, for example, as the trajec-
          tory of a BCI-controlled robotic arm.


          1.3 Functional Near-Infrared Spectroscopy

          Functional near-infrared spectroscopy (fNIRS) differs from EEG and ECoG
          in that it measures the hemodynamic activity rather than electrical brain
          activity, that is, it is a measure of blood flow. Specifically, it measures the
          degree of tissue oxygen saturation and changes in hemoglobin volume using
          near-infrared light (Ferrari et al., 2004). Near-infrared light (700–1000nm)
          penetrates the skin, subcutaneous fat, skull, and underlying muscle/brain,
          and is either absorbed or scattered within the tissue, with the degree of
          absorption and scatter dependent on, among other things, the ratio of oxy-
          hemoglobin to total hemoglobin within the tissue (Ferrari et al., 2004).
          Since this ratio changes as a result of increased oxygen consumption due
          to, for example, higher mental workload, fNIRS can be used to measure
          the degree of activation of different brain regions.
             A typical fNIRS sensor consists of a light source and a light detector, with
          the two commonly placed on the scalp 3–5cm apart (Ferrari et al., 2004;
          Naseer and Hong, 2015). The source emits a known amount of infrared
          light through the scalp and skull toward the brain, and the detector measures
          the amount of scattered light. Tissue oxygen saturation and brain blood flow
          are then estimated from these optical density measurements via the modified
          Beer-Lambert law (Naseer and Hong, 2015). While the response is slower
          than EEG (often appearing a few seconds after a stimulus), it has the advan-
          tage that it is less susceptible to data corruption by artifacts (e.g., blinks, mus-
          cle activity) and offers better spatial resolution, allowing localization of brain
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