For individuals with severe motor deficiencies, controlling external devices such as robotic arms or wheelchairs can be challenging, as many devices require some degree of motor control to be operated, e.g. when controlled using a joystick. A brain-computer interface (BCI) relies only on signals from the brain and may be used as a controller instead of muscles. Motor imagery (MI) has been used in many studies as a control signal for BCIs. However, MI may not be suitable for all control purposes, and several people cannot obtain BCI control with MI. In this study, the aim was to investigate the feasibility of decoding covert speech from single-trial EEG and compare and combine it with MI. In seven healthy subjects, EEG was recorded with twenty-five channels during six different actions: Speaking three words (both covert and overt speech), two arm movements (both motor imagery and execution), and one idle class. Temporal and spectral features were derived from the epochs and classified with a random forest classifier. The average classification accuracy was 67 ± 9 % and 75 ± 7 % for covert and overt speech, respectively; this was 5-10 % lower than the movement classification. The performance of the combined movement-speech decoder was 61 ± 9 % and 67 ± 7 % (covert and overt), but it is possible to have more classes available for control. The possibility of using covert speech for controlling a BCI was outlined; this is a step towards a multimodal BCI system for improved usability.

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Objective. Despite decades of research on central processing of pain, there are still several unanswered questions, in particular regarding the brain regions that may contribute to this alerting sensation. Since it is generally accepted that more than one cortical area is responsible for pain processing, there is an increasing focus on the interaction between areas known to be involved. Approach. In this study, we aimed to investigate the bidirectional information flow from the primary somatosensory cortex (SI) to the anterior cingulate cortex (ACC) in an animal model of neuropathic pain.19 rats (nine controls and ten intervention) had an intracortical electrode implanted with six pins in SI and six pins in ACC, and a cuff stimulation electrode around the sciatic nerve. The intervention rats were subjected to the spared nerve injury after baseline recordings. Electrical stimulation at three intensities of both noxious and non-noxious stimulation was used to record electrically evoked cortical potentials. To investigate information flow, two connectivity measures were used: phase lag index (PLI) and granger prediction (GP). The rats were anesthetized during the entire study. Main results. Immediately after the intervention (<5 minutes after intervention), the high frequency (γ and γ+) PLI was significantly decreased compared to controls. In the last recording cycle (3-4 hours after intervention), the GP increased consistently in the intervention group. Peripheral nerve injury, as a model of neuropathic pain, resulted in an immediate decrease in information flow between SI and ACC, possibly due to decreased sensory input from the injured nerve. Hours after injury, the connectivity between SI and ACC increased, likely indicating hypersensitivity of this pathway. Significance. We have shown that both a directed and nondirected connectivity between SI and ACC approach can be used to show the acute changes resulting from the SNI model.

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