Haptic Simulation: Tactile Mechanisms, Restoration and Medical
Applications
Yifei He
Northeastern University, Shenyang, Liaoning Province, 110819, China
Keywords: Haptic Simulation, Intracortical Microstimulation, Sensory Restoration.
Abstract: This paper mainly focuses on three sections: tactile capture, tactile restoration, and medical potential
evaluation. It reviews the research progress of haptic simulation technology in the field of neuroscience,
focusing on the mechanisms of tactile capture and restoration based on intracortical microelectrode arrays.
Studies have shown that by integrating functional magnetic resonance imaging (fMRI) and
magnetoencephalography (MEG) technologies, the neural pathways and brain functional areas involved in
tactile perception can be precisely captured. During tactile restoration, microelectrode arrays demonstrate
higher accuracy compared to deep brain stimulation (DBS), especially in tasks requiring fine tactile
perception, enabling subjects to experience natural tactile feedback. Furthermore, multimodal stimulation
integration in the brain significantly enhances the effectiveness of tactile restoration. This technology has
important applications in the rehabilitation of amputees and spinal cord injury patients, as well as in the
treatment of neurodegenerative diseases. Future research should focus on improving the design of
microelectrode arrays to enhance the precision and naturalness of haptic simulation and explore their
integration with artificial intelligence technologies.
1 INTRODUCTION
Haptic simulation technology enhances users'
perception of the external environment by integrating
sensors and visual stimuli. Prosthetic limbs help
amputees regain partial mobility but fall short of
replicating the tactile feedback of natural limbs.
In psychophysical experiments, researchers found
that by stimulating the skin while simultaneously
providing visual stimuli, patients could almost
completely restore their sense of touch (Schultz,
Marasco, & Kuiken, 2009). The core of this discovery
lies in "tricking" the brain into believing the missing
limb still exists, enabling users to operate prosthetics
with the brain's assistance.
Skin electrical stimulation therapy involves
adjusting the frequency and amplitude of electrical
stimulation at the afferent nerve interface and
stimulating the residual nerves connected to the
missing limb to restore prosthetic sensation. A widely
used technique in this therapy is transcutaneous
electrical nerve stimulation (TENS), which targets
peripheral sensory nerves. Normally, the brain
receives signals of touch through afferent nerves.
However, when the residual skin of amputees is
stimulated, these signals can "bypass" the traditional
afferent nerve pathways, allowing amputees to regain
non-corporeal perception (Christie et al., 2017).
Another approach is electrical stimulation of the
brain and spinal cord. Through cortical stimulation,
volunteers have been able to control robotic arms and
achieve very simple pain reflexes (Muheim et al.,
2024). This technique not only benefits prosthetic
operation but also shows progress in treating
neurological diseases such as epilepsy. Compared to
the brain, the spinal cord's simpler distribution
structure makes it easier to operate. Spinal cord
stimulation is more suited for lower-limb amputees,
but its sensitivity to somatosensory resolution
remains a challenge (Kruger, Sininoff, & Witkovsky,
1961).
Currently, electrical stimulation technology offers
promising solutions for both upper and lower limbs.
While progress in temperature and pain perception is
nearing maturity, tactile feedback has yet to reach
natural levels. Scientists are currently employing
hybrid strategies of bionic frequency modulation and
amplitude modulation to enhance the natural
perception of prosthetics (Valle, 2022). Bionic
frequency modulation provides a more natural tactile
experience, while amplitude modulation is more
He, Y.
Haptic Simulation: Tactile Mechanisms, Restoration and Medical Applications.
DOI: 10.5220/0014299600004933
Paper published under CC license (CC BY-NC-ND 4.0)
In Proceedings of the 1st International Conference on Biomedical Engineering and Food Science (BEFS 2025), pages 21-26
ISBN: 978-989-758-789-4
Proceedings Copyright © 2026 by SCITEPRESS Science and Technology Publications, Lda.
21
effective in tasks requiring fine recognition (Valle,
2022).
This paper focuses on the mechanisms of
generating sensation through intracortical
microelectrode arrays, with an emphasis on their
impact on amputees. Microelectrode arrays regulate
abnormal neural circuits in the brain, offering new
therapeutic pathways for patients who have lost
sensation and those with neurodegenerative
diseases.
2 TACTILE CAPTURE
2.1 Methods for Tactile Capture
Before microelectrode array experiments, fixed-
frequency oscillatory stimuli are typically applied to
the subject's limbs while functional magnetic
resonance imaging (fMRI) or
magnetoencephalography (MEG) is used to capture
the subject's tactile perception map. This ensures
precise stimulation and avoids individual differences
(Swan, Gasperson, Krucoff, Grill, & Turner, 2018;
John, 2024; Rickard, 2000; Martijn, van den Heuvel,
Hilleke, & Hulshoff Pol, 2010). This paper primarily
outlines fMRI-based tactile capture processes in
humans.
2.2 Data Collection
Some researchers set EPI scan parameters to multiple
axial slices (approximately 20 slices), with a slice
thickness of about 5 mm and a matrix resolution of 64
× 64 (Rickard, 2000; Cox, & Savoy, 2003).
Anatomical images are obtained using T1-weighted
3D SPGR image acquisition (Rickard, 2000).
2.3 Subjects with Perceptual
Impairments
During the generation of tactile experiences, the brain
integrates tactile stimuli with inputs from other
senses, such as visual stimuli. When individuals
observe their own body parts, tactile stimuli activate
the premotor cortex and intraparietal sulcus, resulting
in the tactile-visual enhancement effect (VET) (Swan,
et al. 2018; Andrea, & Patrick, 2010). Based on VET,
scientists collect data by guiding subjects who cannot
directly perceive tactile sensations through touch to
imagine touch while simultaneously providing visual
stimuli (John, 2024).
2.4 Data Processing and Visualization
fMRI data processing methods include Independent
Component Analysis (ICA), clustering analysis,
large-scale network identification (LSNI), and seed-
based analysis (Martijn et al., 2010; Cox, & Savoy,
2003). The LSNI method can identify functional
networks in about 30% of the cortex (Cox, & Savoy,
2003). Researchers first use MCFLIRT for motion
correction and BET to remove non-brain tissue
(John, 2024). Subsequently, constrained volume-to-
surface mapping methods project fMRI data onto the
pial and white matter surfaces for reconstruction
(John, 2024). By calculating z-scores of upper and
lateral cortical areas and setting minimum z-
thresholds, the distance to S1 can be further
calculated for precise functional area localization
(John, 2024).
2.5 Partial Results of Tactile Capture
Tactile sensations can be classified into three main
categories: mechanical perception, thermal
perception (cold and hot), and pain perception
(Huang & Wu, 2021).
2.6 Mechanical Perception
In touch triggered by mechanoreceptors, the
processing of tactile forms and positions exhibits
hemispheric dominance (Van et al., 2005). In GO and
GL tasks, the left intraparietal sulcus (IPS) processes
tactile forms, while the right temporoparietal junction
(TPJ) processes tactile spatial localization (Van
Boven et al., 2005). The secondary somatosensory
cortex (SII) is the neural basis for learning roughness
and pressure information (Harris, Harris, & Diamond,
2001).
2.7 Thermal Perception
Pathways include the thalamus, primary
somatosensory cortex, anterior cingulate cortex
(ACC), orbitofrontal cortex (OFC), and precuneus
(Xiu et al., 2014).
2.8 Pain Perception
Pain perception is regulated by the medial pain
system, with the ACC being a key structure involved
in generating pain experiences and processing pain-
related emotions and motivation (Xiu et al., 2014).
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2.9 Multisensory Integration
Under multisensory stimulation, enhanced BOLD
signals are observed in multiple brain regions,
including the left ventral and dorsal premotor
cortices, left anterior intraparietal sulcus, left inferior
parietal cortex, left postcentral sulcus, left insula, and
bilateral parietal operculum (Swan et al., 2018).
Subcortical structures involved in multisensory
integration include the left putamen, left thalamus,
and right cerebellum (Swan et al., 2018). These
regions are highly interconnected anatomically,
forming the basis for multisensory integration (Swan
et al., 2018).
2.10 Tactile Classification and Decision-
Making
Tactile classification and decision-making are
regulated by different functional subdivisions of the
supramarginal gyrus (SMG) in the parietal lobe (Lee,
Chung, Kim, & Ryun, 2023). Tactile classification is
influenced by PFt stimulation (rostral SMG), while
decision-making is influenced by PF stimulation
(caudal SMG) (Lee et al., 2023).
3 TACTILE RESTORATION
3.1 Successful Methods for Tactile
Restoration
Due to the VET effect, limbs or prosthetics that
cannot perceive touch are typically touched during
brain stimulation to provide visual stimuli
concurrently (Swan et al., 2018; Andrea, & Patrick,
2010). Tactile restoration can be achieved using
microelectrode arrays and deep brain stimulation
(DBS). Compared to DBS, which is suitable for
broader brain region stimulation (eg.Parkinson's
disease treatment) and uses monopolar configurations
(Swan et al., 2018). Microelectrode arrays are better
suited for fine tactile perception and neural repair
tasks, employing bipolar configurations (Swan et al.,
2018). This paper focuses on tactile restoration using
bipolar-configured microelectrode arrays.
3.2 Implantation Method
In related surgeries, the initial stimulation signal
trajectory is typically mapped while the patient is
awake (Swan et al., 2018). Commonly targeted
locations are 2 3 mm posterior to the planned
ventral intermediate nucleus (VIM) treatment
trajectory, close to the visual cortex (VC) and sensory
thalamus (Swan et al., 2018; Downey et al., 2024).
Individual tactile capture results can influence these
implantation locations. Additionally, tapered
electrode arrays are recommended due to their
significantly lower risk of cellular damage compared
to blunt or angled arrays (McNamara et al., 2024).
3.3 Bipolar Configuration Stimulation
Signal Mode
Most experiments use asymmetric bidirectional pulse
sequences (BPS) (Swan et al., 2018; İsmail, Sevgi, &
Burak, 2021). BPS consists of two currents or voltage
pulses opposite in polarity, typically alternating
between a positive and negative pulse. This design
effectively reduces DC bias, minimizing the risks of
tissue damage.
3.4 Bipolar Configuration Stimulation
Signal Duration
The stimulation signal duration is typically greater
than 500 milliseconds, as the minimum time required
to activate specific neurons is generally around this
threshold (Libet et al., 1991). Longer stimulation
ensures the successful activation of neurons and
provides more precise sensory feedback for
subjects (Libet et al., 1991).
3.5 Bipolar Configuration Stimulation
Signal Frequency
Frequency modulation is primarily associated with
the roughness of perceived textures and the number
of neurons activated within the cortical volume
(Greenspon et al., 2024). In human studies,
stimulation at a constant frequency of 100 Hz to 300
Hz typically results in sensations of light touch,
pressure, or mild pricking without triggering
vibratory sensations (Swan et al., 2018). For vibration
perception, frequencies below 100 Hz are usually
selected. For example, studies on rats have shown 40
Hz stimulation induces vibratory effects (İsmail et al.,
2021; Öztürk, Devecioğlu, & Güçlü, 2023).
3.6 Bipolar Configuration Stimulation
Signal Amplitude
Amplitude modulation correlates with the perceived
pressure intensity and the cortical volume activated
(Greenspon et al., 2024). In human experiments,
Haptic Simulation: Tactile Mechanisms, Restoration and Medical Applications
23
when the current amplitude is set between 2575 μ
A, participants generally report sensations of light
touch, pressure, or mild pricking (Swan et al., 2018).
Increasing the current incrementally can enhance the
sensation's intensity and potentially induce pain when
thresholds are exceeded.
3.7 Location and Size of the Perceived
Sensation
The sensation area triggered by different electrodes
and participants varies significantly (Greenspon et al.,
2024). Existing data show that the average sensory
area induced by a single wire for participants is
approximately 14 cm², ranging from 1 cm² to 120
cm² (Swan et al., 2018).
3.8 Processing of Tactile Restoration
Results
3.8.1 Statistical analysis
Data variability is represented by standard error (SE),
and differences in task accuracy, task types, and test
modes are analyzed using two-tailed t-tests (Van
Boven et al., 2005). Researchers adjust significance
levels based on the number of comparisons (eg.some
set α to 0.05) and use Bonferroni correction
methods to control experimental error rates while
reporting differences at p < 0.005 (Van Boven et al.,
2005; Harris et al., 2001).
3.8.2 Quantitative and qualitative analysis
Behavioral data collected during experiments are
analyzed using mixed-effects models, considering the
task as a fixed factor and participants as random
factors (Swan et al., 2018). Quantitative analyses
record the size of the sensory area and classify the
distribution of sensation. Qualitative analyses
categorize sensory qualities based on patient
descriptions into natural pressure, touch, pricking,
and vibration (Swan et al., 2018). Additionally, the
effects of various stimulation modes (eg. constant
frequency, increasing frequency ramp, decreasing
frequency ramp, vibration modes) on the perceived
naturalness of the sensations are compared (Swan et
al., 2018; Öztürk et al., 2023).
4 EVALUATION OF MEDICAL
AND REHABILITATION
APPLICATIONS
4.1 Associated Technologies
4.1.1 Tactile Bionics Technology
To simulate natural tactile feedback, scientists have
proposed bionic designs, including bionic frequency
modulation and amplitude modulation (Valle, 2022).
Specific signal details have been discussed
previously. Experiments demonstrate that tactile
bionic feedback induced by intracortical
microstimulation aligns with the sensorimotor loop,
improving the grasping ability of patients with severe
sensory loss (Swan et al., 2018; Flesher et al., 2021).
Additionally, cortical electrical stimulation
enables volunteers to control robotic arms, achieving
basic pain reflexes (Muheim et al., 2024). Compared
to traditional tactile creation methods (eg. rubber
hand illusion via touch), computer-stimulated "rubber
hand" illusions occur in shorter durations, presenting
additional challenges for tactile restoration (Collins et
al., 2017).
4.1.2 Tactile-Assisted Recognition
Technology
Dynamic tactile feedback systems rely on computer
vision to identify the characteristics of the touched
object. Bionic tactile sensors trained with absolute
fluid pressure, dynamic fluid pressure, temperature,
and thermal flux can differentiate various materials,
including frequencies ranging from 0 140 Hz
(Huang, & Wu, 2021). Hershey lens, an AI camera
module, has been used to learn and identify colors,
facial features, and objects (Wang, Patnik, Wong,
Wong, & Wong, 2018). Future applications anticipate
observing tactile patterns and offering more
intelligent tactile recognition systems.
4.2 Treatment of Related Diseases
4.2.1 Patients with Sensory Loss
Amputees lose limbs and often experience phantom
limb pain. Through the VET effect, the brain can be
tricked into perceiving the presence of limbs, creating
an illusion of still having the missing body part (Swan
et al., 2018; Andrea, & Patrick, 2010). While TENS
is widely used to enhance tactile perception in
amputees, intracortical microelectrode stimulation
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offers more precise and robust features. For spinal
cord injury and paralysis patients, electrical
stimulation of tactile-related regions in the brain
using microelectrode arrays can activate residual
neural pathways, restoring partial sensory functions
(Kruger et al., 1961). Pain resulting from phantom
limb sensations or spinal cord injuries can also be
alleviated using brain-computer interface (BCI)
technologies, which have demonstrated successful
pain mitigation effects (Yanagisawa et al., 2020;
Yoshida, Hashimoto, Shikota, & Ota, 2016).
4.2.2 Patients with Neurodegenerative
Diseases
Neurodegenerative diseases such as Alzheimer's
Disease (AD) are often accompanied by progressive
loss of cognitive and sensory functions (Toh,
Yolland, Gurvich, Barnes, & Rossell, 2023).
Researchers have successfully mitigated disease
severity in AD mouse models through gentle massage
of the fingers or brushing with soft brushes, using
protocols such as three times daily for 15 minutes
over 15 days (Hossain, Karem, Jafari, Kolb, &
Mohajerani, 2023; Hossain, Karem, Jafari, Kolb, &
Mohajerani, 2023). Notably, tactile stimulation for
newborns carrying relevant genes yielded better
results (Hossain et al. 2023).
For Parkinson s Disease (PD), perceptual
disturbances often impair recognition ability. Tactile
illusions may further reduce patients
differentiation ability (Toh et al., 2023). Scientists
have addressed freezing of gait (FOG) in PD patients
by deploying vibrating socks to provide tactile hints,
alleviating symptoms (Brodie et al., 2023). While
DBS remains widely used for neurodegenerative
disease treatment, brain microelectrode stimulation
offers stronger and more precise effects. Tactile
stimulation introduced by microelectrode arrays
holds promise as an auxiliary therapy for
neurodegenerative diseases in the future.
5 CONCLUSION
Haptic simulation, by combining sensors, visual
stimuli, and electrical stimulation technologies, offers
possibilities for restoring tactile sensations in patients
who have lost sensation. In tactile capture,
researchers integrate fMRI and MEG technologies for
localization and employ methods like Independent
Component Analysis and seed-based analysis for
further study. Tactile restoration relies primarily on
microelectrode arrays for fine tactile perception and
incorporates multimodal input through the VET
effect.
The advantage of microelectrode arrays lies in
their higher suitability compared to DBS for
achieving fine tactile perception tasks, and their
bipolar stimulation configuration effectively reduces
risks of tissue damage. By frequency and amplitude
modulation, experimental participants perceive
natural touch, pressure, and mild pricking sensations.
The integration of haptic simulation with brain
microelectrode arrays has demonstrated broad
application prospects in the treatment of amputees,
spinal cord injury patients, paralysis patients, and
neurodegenerative disease patients.
In terms of implementation difficulty, the
technology requires invasive surgical implantation of
microelectrode arrays in patients while awake. The
large variability among individuals also presents
challenges to standardization. Future research should
focus on further optimizing microelectrode array
designs to improve precision and naturalness of
tactile restoration. The integration of AI and
neuroscience holds immense potential for the future
of tactile simulation technology.
REFERENCES
Andrea, S., & Patrick, H. 2010. Touch and the body.
Neuroscience & Biobehavioral Reviews, 34(2), 224-
236.
Brodie, M. A., Pelicioni, P. H., Okubo, Y., Chan, D. Y.,
Carroll, V., Toson, B., Vigano, D., Macagno, M.,
Sternberg, S., Schreier, G., & Lovell, N. H. 2023.
Immediate effects of lower limb sensory simulation
using smart socks to stabilize gait in people with
Parkinson's disease. Annual International Conference
of the IEEE Engineering in Medicine and Biology
Society, 2023, 1–4.
Christie, B. P., Freeberg, M., Memberg, W. D., Pinault, G.
J. C., Hoyen, H. A., Tyler, D. J., & Triolo, R. J. 2017.
Long-term stability of stimulating spiral nerve cuff
electrodes on human peripheral nerves. Journal of
Neuroengineering and Rehabilitation, 14(1), 70.
Collins, K. L., Guterstam, A., Cronin, J., Olson, J. D.,
Ehrsson, H. H., & Ojemann, J. G. 2017. Ownership of
an artificial limb induced by electrical brain
stimulation. Proceedings of the National Academy of
Sciences, 114(1), 166–171.
Cox, D. D., & Savoy, R. L. 2003. Functional magnetic
resonance imaging (fMRI) "brain reading": Detecting
and classifying distributed patterns of fMRI activity in
human visual cortex. NeuroImage, 19(2 Pt 1), 261-270.
Downey, J. E., Schone, H. R., Foldes, S. T., Greenspon, C.,
Liu, F., Verbaarschot, C., Biro, D., Satzer, D., Moon, C.
H., Coffman, B. A., Youssofzadeh, V., Fields, D.,
Hobbs, T. G., Okorokova, E., Tyler-Kabara, E. C.,
Haptic Simulation: Tactile Mechanisms, Restoration and Medical Applications
25
Warnke, P. C., Gonzalez-Martinez, J., Hatsopoulos, N.
G., Bensmaia, S. J., Boninger, M. L., Gaunt, R. A., &
Collinger, J. L. 2024. A roadmap for implanting
microelectrode arrays to evoke tactile sensations
through intracortical microstimulation. medRxiv.
Flesher, S. N., Downey, J. E., Weiss, J. M., Hughes, C. L.,
Herrera, A. J., Tyler-Kabara, E. C., Boninger, M. L.,
Collinger, J. L., & Gaunt, R. A. 2021. A brain-computer
interface that evokes tactile sensations improves robotic
arm control. Science, 372(6544), 831–836.
Greenspon, C. M., Valle, G., Shelchkova, N. D., Hobbs, T.
G., Verbaarschot, C., et al. 2024. Evoking stable and
precise tactile sensations via multi-electrode
intracortical microstimulation of the somatosensory
cortex. Nature Biomedical Engineering.
Harris, J. A., Harris, I. M., & Diamond, M. E. 2001. The
topography of tactile learning in humans. Journal of
Neuroscience, 21(3), 1056-1061.
Hossain, S. R., Karem, H., Jafari, Z., Kolb, B. E., &
Mohajerani, M. H. 2023. Early tactile stimulation
influences the development of Alzheimer's disease in
gestationally stressed APP NL-G-F adult offspring NL-
G-F/NL-G-F mice. Experimental Neurology, 368,
114498.
Hossain, S. R., Karem, H., Jafari, Z., Kolb, B. E., &
Mohajerani, M. H. 2023. Tactile stimulation improves
cognition, motor, and anxiety-like behaviors and
attenuates the Alzheimer's disease pathology in adult
APPNL-G-F/NL-G-F mice. Synapse, 77(2), e22257.
İsmail, D., Sevgi, Ö., & Burak, G. 2021. Intracortical
microstimulation for tactile feedback in awake
behaving rats. In B. Güçlü (Ed.), Somatosensory
Feedback for Neuroprosthetics (pp. 379-411).
Academic Press.
Kruger, L., Siminoff, R., & Witkovsky, P. 1961. Single
neuron analysis of dorsal column nuclei and spinal
nucleus of trigeminal in cat. Journal of
Neurophysiology, 24(4), 333-349.
Lee, D. H., Chung, C. K., Kim, J. S., & Ryun, S. 2024.
Unraveling tactile categorization and decision-making
in the subregions of supramarginal gyrus via direct
cortical stimulation. Clinical Neurophysiology, 158,
16-26.
Libet, B., Pearl, D. K., Morledge, D. E., Gleason, C. A.,
Hosobuchi, Y., & Barbaro, N. M. 1991. Control of the
transition from sensory detection to sensory awareness
in man by the duration of a thalamic stimulus. Brain,
114(4), 1731-1757.
McNamara, I. N., Wellman, S. M., Li, L., Eles, J. R., Savya,
S., Sohal, H. S., Angle, M. R., & Kozai, T. D. Y. 2024.
Electrode sharpness and insertion speed reduce tissue
damage near high-density penetrating arrays. Journal of
Neural Engineering, 21(2).
Muheim, J., Iberite, F., Akouissi, O., Monney, R.,
Morosato, F., Gruppioni, E., Micera, S., & Shokur, S.
2024. A sensory-motor hand prosthesis with integrated
thermal feedback. Med, 5(2), 118-125.e5.
Öztürk, S., Devecioğlu, İ., & Güçlü, B. 2023. Bayesian
prediction of psychophysical detection responses from
spike activity in the rat sensorimotor cortex. Journal of
Computational Neuroscience, 51(2), 207–222.
Rickard, T. C., Romero, S. G., Basso, G., Wharton, C.,
Flitman, S., & Grafman, J. 2000. The calculating brain:
An fMRI study. Neuropsychologia, 38(3), 325-335.
Swan, B. D., Gasperson, L. B., Krucoff, M. O., Grill, W.
M., & Turner, D. A. 2018. Sensory percepts induced by
microwire array and DBS microstimulation in human
sensory thalamus. Brain Stimulation, 11(2), 416-422.
Toh, W. L., Yolland, C., Gurvich, C., Barnes, J., & Rossell,
S. L. 2023. Non-visual hallucinations in Parkinson's
disease: A systematic review. Journal of Neurology,
270(6), 2857–2889.
Valle, G. 2022. Peripheral neurostimulation for encoding
artificial somatosensations. European Journal of
Neuroscience, 56(10), 5888-5901.
Van Boven, R. W., Ingeholm, J. E., Beauchamp, M. S.,
Bikle, P. C., & Ungerleider, L. G. 2005. Tactile form
and location processing in the human brain.
Proceedings of the National Academy of Sciences,
102(35), 12601-12605.
Wang, L., Patnik, A., Wong, E., Wong, J., & Wong, A.
2018. OLIV: An artificial intelligence-powered
assistant for object localization for impaired vision.
Journal of Computational Vision and Imaging Systems,
4(1), 3.
Yanagisawa, T., Fukuma, R., Seymour, B., Tanaka, M.,
Hosomi, K., Yamashita, O., Kishima, H., Kamitani, Y.,
& Saitoh, Y. 2020. BCI training to move a virtual hand
reduces phantom limb pain: A randomized crossover
trial. Neurology, 95(4), e417–e426.
Yoshida, N., Hashimoto, Y., Shikota, M., & Ota, T. 2016.
Relief of neuropathic pain after spinal cord injury by
brain-computer interface training. Spinal Cord Series
and Cases, 2, 16021.
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