- Open Access
Motor priming in virtual reality can augment motor-imagery training efficacy in restorative brain-computer interaction: a within-subject analysis
© The Author(s). 2016
Received: 9 December 2015
Accepted: 12 July 2016
Published: 9 August 2016
The use of Brain–Computer Interface (BCI) technology in neurorehabilitation provides new strategies to overcome stroke-related motor limitations. Recent studies demonstrated the brain's capacity for functional and structural plasticity through BCI. However, it is not fully clear how we can take full advantage of the neurobiological mechanisms underlying recovery and how to maximize restoration through BCI. In this study we investigate the role of multimodal virtual reality (VR) simulations and motor priming (MP) in an upper limb motor-imagery BCI task in order to maximize the engagement of sensory-motor networks in a broad range of patients who can benefit from virtual rehabilitation training.
In order to investigate how different BCI paradigms impact brain activation, we designed 3 experimental conditions in a within-subject design, including an immersive Multimodal Virtual Reality with Motor Priming (VRMP) condition where users had to perform motor-execution before BCI training, an immersive Multimodal VR condition, and a control condition with standard 2D feedback. Further, these were also compared to overt motor-execution. Finally, a set of questionnaires were used to gather subjective data on Workload, Kinesthetic Imagery and Presence.
Our findings show increased capacity to modulate and enhance brain activity patterns in all extracted EEG rhythms matching more closely those present during motor-execution and also a strong relationship between electrophysiological data and subjective experience.
Our data suggest that both VR and particularly MP can enhance the activation of brain patterns present during overt motor-execution. Further, we show changes in the interhemispheric EEG balance, which might play an important role in the promotion of neural activation and neuroplastic changes in stroke patients in a motor-imagery neurofeedback paradigm. In addition, electrophysiological correlates of psychophysiological responses provide us with valuable information about the motor and affective state of the user that has the potential to be used to predict MI-BCI training outcome based on user’s profile. Finally, we propose a BCI paradigm in VR, which gives the possibility of motor priming for patients with low level of motor control.
Brain-Computer Interfaces (BCIs) are communication systems capable of establishing an alternative pathway between user’s brain activity and a computer system. The most common signal acquisition technology in BCI is the non-invasive electroencephalography (EEG) . The EEG activity is distinguished by different wave patterns in the frequency domain called EEG bands or rhythms. These EEG rhythms are divided into different ranges including Alpha (8 Hz - 12 Hz), Beta (12 Hz - 30 Hz), Theta (4 Hz - 7 Hz), and Gamma (25 Hz - 90 Hz) and each rhythm had been found to be related with sensorimotor and/or cognitive states [2, 3]. Rhythms in the Alpha and Beta frequency bands are functionally related to major sensorimotor systems  which are activated primarily through motor preparation or execution . Alpha and Theta oscillations are known to reflect cognitive and memory performance [6, 7], and Theta was shown by early EEG studies to be closely related with problem solving, perceptual processing and learning . Finally, Gamma rhythm has been shown to be modulated during volitionally meditation, consciousness, and sense of self . In addition, decreased levels of Gamma is observed in children with ADHD , in Alzheimer's Disease (AD), and also in epileptic patients . Overall, EEG signals offer low spatial resolution measures of neural activity that occurs in the cortical area of the brain. Translating cognitive states or motor intentions from different rhythms is a complex process and is impossible to associate a single frequency range or cortical location to a brain function.
For BCIs, this oscillatory brain activity -recorded through EEG- is currently used for the interfacing between humans and computers. This communication can be triggered by an exogenous stimulus through visual, auditory or sensory feedback, like Steady State Visual Evoked Potentials (SSVEP) and P300. SSVEP is caused by visual stimulation of flashing lights and occur at the primary visual cortex of the brain . Instead, P300 responses are generated by measuring the brain evoked responses 300 ms after stimulus onset (hence the name) . In contrast to exogenous sources, motor-imagery (MI) BCI is of endogenous origin and makes use of the visuo-motor imagination (imagination of upper and/or lower limb movement). MI has been shown to share common control mechanisms and neural substrates of actual movement both in action execution and action observation , providing a unique opportunity to study neural control of movement in either healthy people or patients [15, 16]. Therefore, MI has been widely used as the main BCI paradigm in research  for individuals with high degree of motor disability or locked-in syndrome [18, 19]. To date, MI is proven useful in a wide area of applications ranging from accessibility tools for disabled users with paralysis or severe neuromuscular disorders , for restoration of active movement , to human-computer interaction research , virtual reality and video games .
In stroke rehabilitation, BCIs have been mostly used with two different strategies. The first one is the “assistive”, which aims at bypassing non-functional corticospinal pathways for controlling robotic prosthetics . The second is the “restorative”, which aims at mobilizing neuroplastic changes in order to achieve the reorganization of motor networks to attain functional motor recovery . For the latter case, MI-BCI training has been the most widely used BCI paradigm . Results from previous studies have proven mental practice of action to be useful in MI-BCI training . MI training is leading to the activation of overlapping brain areas with actual movement, and because sensory and motor cortices can dynamically reorganize through neuroplasticity [26, 27], MI constitutes an important component for motor learning and recovery. Moreover, research about the mirror neuron system (MNS) have shown that action observation, motor imagery, and imitation share the same basic motor circuit as action execution and thus provide an additional or alternative source of motor training that may be useful to promote recovery from stroke . In addition, it has been found that the spatial distribution of local neuronal population activity during MI mimics the spatial distribution of activity during actual motor movements . Beneficial effects of MI in motor control have been shown , and new paradigms have been proposed to maximize the recruitment of motor networks . In stroke rehabilitation, the combination of BCIs with virtual environments has gained popularity, and it has been shown very useful to train functional upper limb pointing movements [31, 32]. Unfortunately, MI-BCI studies for stroke rehabilitation are very different in terms of (a) experimental design and (b) research protocols. So far in MI training, the use of abstract feedback in the form of unidirectional arrows as the main visual feedback mechanism is the most widely used . Although there is no direct evidence that different feedback designs, i.e. realistic grasping with a hand vs. extending arrows, imply differences in performance in MI , previous studies have shown that the type of feedback can have different effects based on the learner . For instance, emotional feedback (in the form of smiley faces) has shown positive results in MI performance . Other researchers have studied the effect of alternative feedback modalities on a BCI task, such as haptic and auditory feedback, with inconclusive results [36, 37]. Interestingly, it has been shown that the combination of audio and visual feedback decreases BCI performance, whereas the combination of haptic and visual feedback increases the performance [38, 39]. In another experiment, displaying real-time cortical activity as neurofeedback was shown to significantly increase MI performance . Furthermore, videogames and Virtual Reality (VR) feedback has also produced positive results, offering a more compelling experience to the user through 3D environments [22, 41]. The fusion of BCI and VR (BCI-VR) allows a wide range of experiences where participants can control various aspects of their environment -either in an explicit or implicit manner-, by using mental effort alone. This direct brain-to-VR communication can be used to induce illusions mostly relying on the sensorimotor contingencies between perception and action . Friedman et al., in a study from 2007, included three different BCI setups: (i) abstract feedback, (ii) head-mounted display (HMD), and (iii) the CAVE-like system. They did not find any consistent performance trend related to the type of interface, but the event-related synchronization (ERS) was stronger in the CAVE setup .
Despite the increased attention that BCI technology has had with the launch of low-cost commercial EEG devices in the last few years, BCI technology is hardly used outside laboratory environments . Unfortunately, BCIs are not yet as accurate as other types of interfaces , and users require a training period up to several months to achieve accuracies of 65 %–80 % using cortical potentials . Although accuracy varies among the different BCI paradigms, most are not 100 % accurate, they require extensive training, and have low information transfer rates and long response delays . For instance, MI-BCI requires long training trials and settings are subject specific. As consequence, long and repetitive training sessions can result in user fatigue and declining performance over time. In addition, prolonged training is problematic in generating the EEG oscillatory rhythms modulated during MI, such as Mu and Beta rhythms . New findings in MI experimentation have shown that increased vividness of imagery is strongly associated with the neural activity in motor related areas  and that the kinesthetic imagination of movement is preferable over just visual imagination, resulting in increased MI-BCI performance . Unfortunately, there is a limited understanding on how these factors affect the activity patterns of motor related areas. Recent studies have shown that physical activity prior to a MI task (motor priming) facilitates the engagement of motor networks on the subsequent MI task . It has been shown that during feedback presentation EEG synchronization patterns increase hemispheric asymmetry compared to control sessions without feedback . In addition, hemispheric asymmetry is related with increased performance of fine motor tasks, and specifically left hemisphere changes are related to motor learning . However, different studies had different experimental setups and it is not clear how we can improve the design of a MI-BCI paradigm. Moreover, there is a lack of systematic studies dedicated to the actual aspects of the experimental (training) task, focusing mostly on the technical aspects of the system. Therefore, in the area of neurorehabilitation there is an urgent need to identify the key elements for a successful MI-BCI training using specific criteria for motor rehabilitation for including patients with severe hemiparesis. This leads to questions such as, (1) How can we include patients with low level of motor control, (2) how can we maximize both performance and sensorimotor activation, and (3) how can we promote adherence to MI-BCI training?
In order to overcome some of the limitations of current BCI systems, we performed a study based on a novel prototype that makes use of multimodal feedback, in an immersive VR environment delivered through a state-of-the-art Head Mounted Display (HMD), integrated in a MI-BCI motor training task (left | right hand imagery) . To achieve maximum engagement of sensory-motor networks in a MI-BCI motor rehabilitation task, we assessed the role of motor priming and multimodal VR feedback compared to a control condition. In this study we included naïve subjects, with no previous exposure in BCI, in order to have a first-time user experience (FTUE).
Through an immersive multimodal VR environment and motor priming, we can maximize the engagement of sensory-motor networks important in neurorehabilitation, due to the enhanced modulation of the same cortical areas that are activated during actual motor preparation and execution.
We can quantify the relationship between users’ electrophysiological data and psychophysiological responses, important for identifying which patient profile can benefit the most from an immersive BCI-VR setup for MI training.
In our design of the BCI setup, we incorporated properties that are recommended as a good instructional design in BCI training . In all conditions we presented the user only with the correct classified action for enhancing the feeling of competence, we provided a clear and meaningful task through the virtual task paradigm, the task was self-explanatory, simplified and intuitive, with progress of achievement, challenging but achievable, and finally in an engaging 3D virtual environment. All 3 BCI conditions were designed based on the Graz-training paradigm . The control condition incorporated the Graz-training with abstract bars-and-arrows feedback, and for the VR version we used ambient and event sounds and a virtual representation of two hands performing the motor action.
Three experimental conditions were designed with different feedback and priming mechanisms: multimodal VR with motor priming, multimodal VR, and standard MI. For all conditions, a total of 10 repetitions (of approximately 4 s duration, followed by a 2 s pause) of motor-execution/mental simulation for each hand were performed and presented always through a HMD.
Multimodal Virtual Reality with Motor Priming (VRMP)
Multimodal Virtual Reality (VR)
In this condition, users were asked to only carry out the MI-BCI calibration block and the online MI-BCI task block as in the previous condition, but without the prior MP (Fig. 2b).
Control - standard motor imagery
In this condition, a standard MI-BCI paradigm was used, providing a control condition for the other conditions to be compared with. Hence, this condition followed the same protocol as the VR condition, but instead of the VR component only simple bar-and arrow-elements without sounds (the so-called Graz visualization) were used as feedback mechanisms (Fig. 2c). Yet, the MI task consisted in the motor imagery of the same upper-limb movements as described in conditions VRMP and VR and was presented through the same HMD.
The experimental setup was composed by a desktop computer (OS: Windows 8.1, CPU: Intel® Core™ i5-4440 at 3.3 GHz, RAM: 8GB DDR3 1600MHZ, Graphics: Nvidia GT 630 1GB GDDR3), running the 3 different MI-BCI training conditions described above. All visual and auditory feedback was developed with the Unity 3D game engine (Unity Technologies, San Francisco, USA). For hand and finger tracking during the MP block, the Leap Motion controller (Leap Motion, Inc., San Francisco, California, United States) was used to map hand and finger movements to the virtual counterparts. A stereo headset for spatial sound was used in VR and VRMP conditions. The Oculus Rift DK1 HMD (Oculus VR, Irvine, California, United States) was used for all conditions, regardless of the feedback modality.
The BCI set up consisted of 8 active electrodes equipped with a low-noise biosignal amplifier and a 16-bit A/D converter at 256 Hz (g.MOBIlab biosignal amplifier, gtec, Graz, Austria). The spatial distribution of the electrodes followed the 10–20 system configuration with the following electrodes over the sensory-motor areas: FC3, FC4, C3, C4, C5, C6, CP3, and CP4. The signal amplifier was connected via bluetooth to a laptop computer (CPU: Intel® Core™ i3-3217U at 1.80 GHz, RAM: 8GB DDR3 1600MHZ, Graphics: Intel® HD Graphics 4000) for the EEG signal acquisition and processing through the OpenVibe platform . For all conditions, a Common Spatial Patterns (CSP) filter was used for feature extraction, based on the mutual diagonalization of each covariance matrix for each class to be discriminated . CSP has been shown to deliver better performance in MI experiments . In addition, Linear Discriminant Analysis (LDA) was used for the classification of the two classes (left | right hand imagery) from the feature vector. LDA reduces the dimensionality of the data and establishes a surface decision in the feature space which separates data into two groups, each one related to one class . Finally, the classified data were transmitted to the RehabNet Control Panel (RehabNetCP)  through the VRPN protocol  to control the virtual environment. The RehabNet Control Panel is a free tool that acts as a device router to bridge a multiple interfaces with virtual environments.
A total of 9 right handed healthy participants (8 male, 1 female) with a mean age of 27 ± 2 years old participated in the study. Participants were recruited based on their motivation to participate, with no previous known neurological disorder. We included only naïve subjects, with no previous exposure in BCI, to have a first-time user experience (FTUE). This was done in order to minimize any bias by previous experienced in MI in neurofeedback and because our target population has no prior BCI exposure. All participants were students and staff from the University of Madeira and were recruited at the Madeira Interactive Technologies Institute. The experiments were approved by the Ethics Committee of the Public Health System of the Autonomous Region of Madeira, Portugal (SESARAM), with decision number: 15/2015. All subjects were informed and signed an informed consent to participate and to publish their data according to the Declaration of Helsinki.
The Presence Questionnaire (PQ) is a tool that measures the degree to which individuals experience presence in a virtual environment and the influence of possible contributing factors to the intensity of the experience . PQ has 24 questions in a seven-point Likert scale to assess items such as realism, possibility to act and sounds. Items related to haptic assessment were excluded because this aspect was not addressed in our experiment.
Vividness of Movement Imagery Questionnaire-2 (VMIQ2)  was used to assess the Kinesthetic Imagery ability of the participant. VMIQ comprises 12 questions to rate vividness of different items in a 5-point scale. Participants had to report how clear was the image obtained by imagining themselves do the following movements (Kinaesthetic imagery): walking, running, kicking a stone, bending to pick up a coin, running up-stairs, jumping sideways, throwing a stone into water, kicking a ball in the air, running downhill, riding a bike, swinging on a rope, and jumping off a high wall. The VMIQ has been previously used to determine differences in neural activation patterns between vivid and non-vivid imagery .
Finally, the NASA TLX questionnaire was used to measure task load through a number of subscales . These subscales include Mental Demands, Physical Demands, Temporal Demands, Performance, Effort and Frustration.
Power Spectral Density (PSD) Estimation
In order to remove major artifacts related with eye blinking and muscular activity, a manual cleaning of the signal in the time domain was performed, followed by a component rejection process. The component rejection was performed by using Independent Component Analysis (ICA) with the help of the EEGLAB toolbox . With the use of ICA we rejected components responsible for major artifacts of either endogenous (muscle, jaw clenching, eye movement) or exogenous source (AC power). EEG rhythms were processed by extracting the Power Spectral Density (PSD) of the signals in Matlab (MathWorks Inc., Massachusetts, US). The power was extracted every 500 ms using Welch’s method with windows of 128 samples for the following frequency bands: Alpha (8 Hz - 12 Hz), Beta (12 Hz - 30 Hz), Theta (4 Hz - 7 Hz), Low Gamma (25 Hz - 45 Hz), and High Gamma (55 Hz - 90 Hz). For the current analysis and because we were only measuring from sensory-motor areas, data were averaged for all the channels for each experimental condition. Moreover, left and right hemisphere electrodes were aggregated to assess hemispheric differences between conditions.
EEG Rhythms: We used the mean PSD from each EEG frequency band for each condition.
MI classifier performance: From the LDA classification accuracy on both the calibration and the online task blocks, we calculated the mean classification accuracy per condition as a percentage.
Workload: We used the sum of all sub-elements of the TLX questionnaire to extract the Workload for each participant on each condition.
Kinesthetic Imagery: We used the sum of all sub-elements per user to extract the overall Kinesthetic Imagery.
Normality of the distribution of all data was assessed using the Shapiro-Wilk (S-W) normality test, recommended for tests with a sample size of less than 50 . For classifier performance, and because the data deviated from normality, non-parametric statistical tests were used for the analysis. For the assessment of overall differences between the three experimental conditions, a Friedman test was used on each dependent variable. For further pairwise comparisons, the Wilcoxon signed-rank test on each of our combinations was used. On EEG rhythm data, the S-W test revealed normality of the data (p > 0.05). We therefore analyzed the data using a repeated measures ANOVA with a Greenhouse-Geisser correction due to Mauchly's Test of Sphericity violation. For all pairwise comparisons a Bonferroni correction was used to account for the number of comparisons. Effect sizes were computed on pairwise comparisons. For all statistical comparisons the significance level was set to 5 % (p < 0.05). All statistical analysis was done using IBM SPSS 20 (SPSS Inc., Chicago, IL, USA).
Spearman correlations were performed between the mean PSD from all EEG rhythms (Alpha, Beta, Theta, Gamma) and questionnaire (Workload, Kinesthetic Imagery, and their sub-domains) data, with a significance level set to 5 % (p < 0.05).
Multivariate linear regression
A Stepwise regression modelling approach was used to identify electrophysiological predictors that provide a good fit based on their statistical significance (p < 0.05) between subjective (questionnaires) and objective (EEG) data. The set of variables that were used for the multivariate linear regression includes (a) the subjective experience as reported through the questionnaires against (b) the EEG rhythms. The Stepwise coefficient estimation of the models was done using Matlab (MathWorks Inc., Massachusetts, US).
In the following section, results concerning EEG activity, classification performance and questionnaire answers are illustrated for all conditions. In addition, electrophysiological correlates between subjective and objective data are assessed in order to understand how we can maximally engage motor areas in an MI-BCI task.
Effect and impact of different MI-BCI experimental paradigms
To assess the difference between all conditions, we compared the different EEG rhythms, the classification score (the ability of the classifier to identify correctly one of the two classes of our motor-imagery task), and the hemispheric asymmetry for (1) motor-execution during MP, (2) VRMP condition, (3) VR condition, and (4) Control condition. In this analysis, (1) and (4) are used both as controls for comparison to standard MI-BCI feedback and to assess resemblance with actual motor-execution. The latter is particularly interesting since we aim for a MI-BCI paradigm that is able to retrain the same motor networks that are responsible for actual movement.
A repeated measures ANOVA determined that mean EEG rhythms differed significantly across conditions for: Alpha (F(2.524, 20.191) = 4.800, p < 0.05), Beta (F(1.599, 12.796) = 7.541, p < 0.05), Theta (F(1.874, 14.990) = 7.615, p < 0.05), low Gamma (F(1.713, 13.701) = 11.639, p < 0.05), and high Gamma (F(1.617, 12.938) = 6.869, p < 0.05) (Fig. 4a). EEG rhythms during calibration show a convergence of brain activation for VR and VRMP conditions towards overt motor-execution. Overall, EEG data show a clear trend with overt motor-execution and Control condition at opposite ends and VR and VRMP in between, being the latter the closest to motor-execution. Post hoc tests revealed that the mean EEG rhythm on the Alpha band differed significantly between VRMP and Control conditions. For the Beta band, a significant difference was found between both motor-execution and VRMP conditions with Control. For the Theta band, motor-execution was significantly different from both VR and Control conditions, and VRMP from Control. In Lower Gamma, motor-execution was significant different from VRMP and VR, as VRMP was significantly different from Control. Interestingly, in Lower Gamma, the above trend was altered, with the mean power of overt motor-execution displaying the lowest values. Finally, for Higher Gamma, there was a significant difference for both motor-execution and VRMP conditions with Control.
Classification ScoreThe MI-BCI calibration data revealed that the multimodal setup with motor priming condition (VRMP) provided the highest performance (Mdn = 65.8, IQR = 3.32) when compared with the VR only condition (Mdn = 64.5, IQR = 5.41) and control condition with the traditional feedback (Mdn = 62.3, IQR = 7.63) (Fig. 3a). However, these differences are small and a Friedman test revealed no statistical difference (χ2(2) = 1.429, p = 0.490).
In the Calibration block, we observe the same convergence pattern towards motor-execution present in the previous EEG analysis for all frequency bands (Fig. 5a). A repeated measures ANOVA determined that mean difference of hemispheric asymmetry, was not statistically significantly different between conditions for calibration, in Alpha (F(2.219, 17.754) = 0.865, p = 0.448), Beta (F(1.905, 15.242) = 0.998, p = 0.388), Theta (F(1.941, 15.528) = 0.960, p = 0.402), low Gamma (F(2.083, 16.667) = 0.719, p = 0.507), and high Gamma (F(2.430, 19.443) = 0.625, p = 0.625);
MI Task Block
EEG RhythmsThe mean EEG rhythms during the MI task block followed a very similar trend as in the calibration block (Fig. 4b), being both blocks significantly correlated for Alpha (r = 0.564, p < 0.01), Beta (r = 0.501, p < 0.01), Theta (r = 0.599, p < 0.01), low Gamma (r = 0.555, p < 0.01), high Gamma (r = 0.635, p < 0.01). The repeated measures ANOVA revealed a significant difference for Theta (F(2.660, 21.277) = 3.520, p < 0.05). Nevertheless, no statistical differences across conditions were found for Alpha (F(2.804, 22.429) = 0.813, p = 0.493), Beta (F(2.628, 21.020) = 2.780, p = 0.72), low Gamma (F(2.434, 19.475) = 3.199, p = 0.055), and high Gamma (F(2.232, 17.860) = 3.071, p = 0.067). Post hoc tests using the Bonferroni correction revealed that there is a trend for VRMP against the control condition (p = 0.073) but not for the rest of the pairwise comparisons. Interestingly, the mean power of the Lower Gamma frequency band was reduced for all MI conditions, showing that EEG activation during the MI task block was more similar to motor-execution than in the calibration block, and hence in accordance with the trend identified in the rest of frequency bands (Fig. 4).
In contrast to the calibration block, performance score drops considerably (>10 %) for all conditions during the subsequent MI task block, showing lower performances and higher variability (Fig. 3b). Notably, for VRMP, performance dropped to Mdn = 51.29 (IQR = 6.42), for VR to Mdn = 53.61 (IQR = 12.99) and in Control condition to Mdn = 50.1 (IQR = 7.23).
Hemispheric AsymmetryA repeated measures ANOVA determined that mean difference of hemispheric asymmetry was not statistically different between conditions for the MI task, Alpha (F(2.094, 16.754) = 1.210, p = 0.325), Beta (F(2.236, 17.891) = 1.519, p = 0.245), Theta (F(1.878, 15.023) = 1.263, p = 0.309), low Gamma (F(2.299, 18.393) = 1.047, p = 0.380), and high Gamma (F(2.287, 18.296) = 1.086, p = 0.366) (Fig. 5b).
Quality of the experience
Realism of the VR Training SimulationBoth VRMP and VR conditions share the same virtual environment for which users were asked to report their sense of presence. The normalized score of the Presence Questionnaire (PQ) indicates an overall acceptance of the VR task (M = 94.3 %, SD = 8.3) (Fig. 6). Overall, four out of the five domains considered scored above 70 %: realism (M = 73 %, SD = 8), the possibility to act through initiated actions and events (M = 77 %, SD = 14), sounds of the VR task (M = 79 %, SD = 12), and the self-evaluation of performance, which had the highest score (M = 83 %, SD = 9). The quality of the interface showed the lowest score (M = 58 %, SD = 13). Nevertheless, the quality of the interface did not seem to affect the high perceived performance and realism of the VR task.
Correlates of Workload, Kinesthetic Imagery and Task EngagementAfter the MI task block on each condition, the perceived Workload was assessed through the NASA TLX questionnaire and the Kinesthetic Imagery ability through the VMIQ-2 questionnaire. A repeated measures ANOVA determined that mean Workload differed significantly across conditions (F(1.505, 12.036) = 5.290, P < 0.05) (Fig. 7). Post hoc tests revealed that Workload in the VRMP condition to be significantly higher than for Control. A correlation analysis revealed no correlation between Workload and the performance during the MI task block.Kinesthetic Imagery was assessed through the VMIQ-2 questionnaire. The cut-off-point established by Whetstone estimates good imagery ability with a total score of 70 % . Our experiment considered only first-time user experiences, and the average ability score was 61.36 % (SD = 12) and only 3 out of 9 subjects scored above 70 %. A comparison among conditions showed that conditions did not affect the participant’s ability to create clear and vivid motor imagery (F(1.567, 12.532) = 1.292, p = 0.300) (Fig. 8). A correlation analysis showed no significant correlation between Kinesthetic Imagery and the performance during the MI task block.
Relationship between EEG rhythms and subjective experience
Correlation AnalysisConsidering only the EEG data during the MI task block, we identified correlations of Alpha and Theta bands with the subjective reports (Table 1). For the TLX subcomponent of Mental Demand we found a significant correlations with Alpha (r = 0.500, p < 0.05) and Theta (r = 0.555, p < 0.05). Negative correlations were found for Alpha with the reported Kinesthetic Imagery ability in Jumping Sideways (r = −0.381, p < 0.05) and Running Downhill (r = −0.420, p < 0.05), and for Theta only for Running Downhill Kinesthetic Imagery (r = −0.545, p < 0.05).Table 1
Correlation table from MI task EEG data including Alpha and Theta bands with TLX and its subdomains
TLX - Mental Demand
KI - Jump Sideways
KI – Run Downhill
Multilinear Regression ModellingA stepwise regression modelling was used to identify electrophysiological predictors of subjective experience based on EEG PSD and questionnaire data (Table 2). Mental Demand was found to relate to a combination of Theta and Beta bands (F(2, 24) = 8.894, p < 0.05, R 2 = 0.426). Interestingly, although both Alpha and Theta bands were shown to positively correlate with Mental Demand, this is better explained through Beta and Theta. This may indicate collinearity between Alpha and Theta bands. For Kinesthetic Imagery, Alpha band modulation is related to the user’s capacity for mental imagery that involves sideways jumps (F(1, 25) = 4.607, p < 0.05, R 2 = 0.156), and Beta and Theta for mental imagery that involves running downhill (F(2, 24) = 10.606, p < 0.05, R 2 = 0.469).Table 2
Stepwise model coefficients from online data
TLX – Mental Demand
KI – Jump sideways
KI – Run downhill
x1 : Alpha
x 2 : Beta
x3 : Theta
The obtained results contribute with a set of important findings in several dimensions: quantification of EEG modulation and classification through VR feedback and MP, and how those relate to perceived experience and Kinesthetic Imagery ability. These findings may be important to enhance the impact of MI-BCI in neurorehabilitation and push the state-of-the-art.
Firstly, through the analysis of EEG rhythms we compared VR and VRMP conditions with (1) a standard control condition using Graz visualization and (2) actual EEG activity during overt motor-execution. Our EEG data revealed statistically significant differences of VRMP with standard feedback, suggesting the engagement of different underlying processes, more consistent with motor-execution data. The differences in Alpha and Beta with control and their similarity with the activity induced during motor-execution is of high importance for MI training in rehabilitation due to better association to cortical activation of sensorimotor areas during voluntary movement [66, 67]. Furthermore, increased activity in Alpha and Theta could indicate an effect of increased cognitive and memory load in VR , as also shown in our study through TLX data. However, despite measurable differences in EEG activity among conditions, these did not significantly change the classification performance of the LDA used for BCI control.
We also observed in our hemispheric asymmetry analysis that interhemispheric communication changed during the different MI-BCI paradigms. Previous studies have shown that the hemispheric asymmetry increases during feedback presentation compared to sessions without feedback , enhances the performance of fine motor tasks and triggers changes in motor learning . A recent study highlights that the left hemisphere is specialized for sequential motor organization in both left- and right-handers, suggesting an endogenous hemispheric asymmetry related to compound actions and skill representation . Therefore, if interhemispheric communication can be modulated through VRMP as our data suggests, this is an important feature to be utilized in motor learning. In patient populations with affected hemispheric differences we could promote increased interhemispheric interaction by balancing the activation of motor-areas and influence motor performance . In addition, interhemispheric interactions may also contribute to intermanual transfer, as it has been found that motor learning using one hand improves the performance of the other hand [70, 71]. Therefore, longitudinal neuroimaging and electrophysiological studies are necessary in order to demonstrate the dynamic change in interhemispheric interaction between both hemispheres during the process of functional recovery in stroke survivors.
Secondly, subjective data reported through questionnaires allowed us to report on their relationship with EEG data, providing insights of the effect of different MI conditions in both of cognitive and motor processes. Interestingly, although in the VRMP condition the user had to exert more physical activity, our data revealed that Physical Demand and Effort subcomponents of the TLX were not affected. We argue that the inclusion of the MP component within an immersive VR environment turned the MI-BCI task into a more mentally demanding task, with the potential of engaging more neural circuits than in the other 2 conditions. This hypothesis is also supported by the differences found in the EEG activity patterns. Additionally, we found a correlation between Kinesthetic Imagery ability and their capacity to display enhanced activity in the Alpha and Beta bands, which are modulated during cortical activation/deactivation in the planning of voluntary movement [72, 73]. Finally, enhanced sensory-motor rhythms through MI-BCI training have been shown in patients displaying higher motor improvements as assessed by the Fugl-Mayer . Thus, our findings give further support to the importance of the vividness of motor-imagery capability in MI-BCI training, −especially the walking components of the questionnaire (jump, run)-, enabling us to use them as inclusion criteria in a neurorehabilitation MI-BCI paradigm, considering that their reliability has been assessed in both healthy and post-stroke people .
Our findings are aligned with previous research, verifying that abstract feedback versus realistic, can have very little effect in terms of BCI classification performance, but showing that BCI feedback clearly modulates sensorimotor EEG rhythms . This could lead towards better functional outcomes compared with standard MI as reported by previous research .
Our current results are based on the premise that it is possible to modify EEG rhythms through multimodal feedback, affecting the activity of somatosensory and motor areas for the better. This is a proposition for which there is limited empirical evidence so far. We found consistent performance trends related to the type of interface but also enhanced EEG rhythms modulation through immersive VR and motor priming. Overall, we showed that, both VR conditions elicited an increase of mean power in all EEG rhythms. Although it is known that motor-imagery involves to a large extent the same cortical areas that are activated during actual motor preparation and execution , we have shown that motor-imagery training in a multimodal setup and priming (VRMP) can provide the strongest and most similar motor network activation to overt movement-execution from all tested MI-BCI training paradigms. Furthermore, the activation of ipsilateral (contralesional) primary sensorimotor cortex (SMC) and the mirror neuron system (MNS) appears to play a fundamental role in both action execution and imitation [67, 76, 77] enhanced by VR. With current findings in hemispheric asymmetry, we can distinguish the important role of interhemispheric communication in motor learning.
Moreover, by assessing the quality of the experience, we observed a high overall acceptance of the novel multimodal MI paradigms, despite a reported increase in Workload. By modeling electrophysiological data and perceived experience data, we are able to better describe the relationship between user profile (Kinesthetic Imagery ability, perceived Workload, Presence in VR) and EEG rhythms changes in response to MI-BCI training, which may become very relevant to identify which patients can benefit the most from it.
In practice, satisfactory BCI control depends largely on the degree to which neural activity can be voluntarily controlled by users. Therefore, approaches to the training of users to control a BCI taking into consideration the specific target population play an important role. In the case of stroke survivors, our approach is based on the priming of the sensorimotor system, through realistic VR and training through gamified tasks. For patients with severe hand paresis for who motor priming through movements of the paretic limb is not possible, a VR setup such as ours could offer the ability to mirror the healthy arm during the priming session, with the affected. Mirror therapy is the use of visual illusion created by a mirror by superimposing the intact arm over the paretic. Mirror therapy is well established in stroke rehabilitation for promoting recovery [78, 79]. Therefore, our system could also be used to provide MI driven mirror therapy by mirroring the healthy arm to virtual limbs. Overall, in this study we showed that MI training with multimodal setup and priming (VRMP) is an effective paradigm to elicit sensorimotor activation consistent with motor execution. We showed that thanks to our quantification of the perceived experience in MI-VR training could improve adherence to the treatment by adjusting the VR task to improve the experience. Finally, the proposed VRMP paradigm has a large potential even in the case of patients with no motor control, by exploring the possibilities of MI-BCI driven mirror therapy.
In the future, we plan to run a study with stroke participants in order to evaluate the impact of the proposed VRMP paradigm in motor function restoration. We plan to clinically validate the VRMP paradigm in a longitudinal 1-month MI-BCI study including motor evaluations and pre- and post- functional brain imaging to identify the underlying neural activation and reorganization correlates of motor recovery.
This study, although it results from the collection of 63 EEG datasets, is limited by its sample size (N = 9). Findings have limited statistical power and should be interpreted with caution. Moreover, results from healthy participants cannot be directly generalized to a stroke population, which requires further research. Finally, current data was recorded through 8 EEG electrodes and a limited spatial resolution. An increased amount of electrodes could offer new insights by covering a larger area of the sensorimotor and neighboring areas and with higher resolution.
BCI, brain-computer interface; EEG, electroencephalography; MI, motor-imagery; SMR, sensorimotor rhythm; VR, virtual reality; VRMP, Virtual Reality with Motor Priming
This work was developed at the NeuroRehabLab (http://neurorehabilitation.m-iti.org) and is supported by the European Commission through the RehabNet project - Neuroscience Based Interactive Systems for Motor Rehabilitation - EC (303891 RehabNet FP7-PEOPLE-2011-CIG), by the Fundação para a Ciência e Tecnologia (Portuguese Foundation for Science and Technology) through SFRH/BD/97117/2013, and LARSyS (Laboratório de Robótica e Sistemas em Engenharia e Ciência) through UID/EEA/50009/2013.
This research was supported by the European Commission through the RehabNet project - Neuroscience Based Interactive Systems for Motor Rehabilitation - EC (303891 RehabNet FP7-PEOPLE-2011-CIG), by the Fundação para a Ciência e Tecnologia (Portuguese Foundation for Science and Technology) through SFRH/BD/97117/2013, and LARSyS (Laboratório de Robótica e Sistemas em Engenharia e Ciência) through UID/EEA/50009/2013. The funding bodies supported the design of the study, collection and analysis of the data, as well as the interpretation and the writing of the article.
Availability of data and material
The datasets during and/or analyzed during the current study available from the corresponding author on reasonable request.
AV and SBB defined and designed the research study. AV participated in the development of the software, and AV and SBB designed the technical specifications underlying the different experimental conditions. AV collected and analyzed the data. AV and SBB interpreted the data. SBB supervised the study. All authors revised and approved the current version of the manuscript.
The authors declare that they have no competing interests.
Consent for publication
All subjects signed an informed consent to publish their data and images.
Ethics approval and consent to participate
The experiments were approved by the Ethics Committee of the Public Health System of the Autonomous Region of Madeira, Portugal (SESARAM), with reference number: 15/2015 and signed by the president of CES/SESARAM, Mr. Ricardo Santos . All subjects signed an informed consent to participate in the study and to publish their data and according to the Declaration of Helsinki.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Wolpaw JR, Birbaumer N, McFarland DJ, Pfurtscheller G, Vaughan TM. Brain-computer interfaces for communication and control. Clin Neurophysiol Off J Int Fed Clin Neurophysiol. 2002;113:767.View ArticleGoogle Scholar
- Budzynski TH, Budzynski HK, Evans JR, Abarbanel A. Introduction to Quantitative EEG and Neurofeedback: Advanced Theory and Applications. San Diego, USA: Academic Press; 2009.Google Scholar
- Schomer DL, Silva FHL da Niedermeyer’s Electroencephalography: Basic Principles, Clinical Applications, and Related Fields. Philadelphia, USA: Lippincott Williams & Wilkins; 2011.Google Scholar
- Crone NE, Miglioretti DL, Gordon B, Sieracki JM, Wilson MT, Uematsu S, Lesser RP. Functional mapping of human sensorimotor cortex with electrocorticographic spectral analysis. I. Alpha and beta event-related desynchronization. Brain. 1998;121:2271–99.View ArticlePubMedGoogle Scholar
- Pfurtscheller G, Neuper C. Motor imagery activates primary sensorimotor area in humans. Neurosci Lett. 1997;239:65–8.View ArticlePubMedGoogle Scholar
- Klimesch W. EEG alpha and theta oscillations reflect cognitive and memory performance: a review and analysis. Brain Res Rev. 1999;29:169–95.View ArticlePubMedGoogle Scholar
- Schack B, Vath N, Petsche H, Geissler H-G, Möller E. Phase-coupling of theta–gamma EEG rhythms during short-term memory processing. Int J Psychophysiol. 2002;44:143–63.View ArticlePubMedGoogle Scholar
- Schacter DL. EEG theta waves and psychological phenomena: A review and analysis. Biol Psychol. 1977;5:47–82.View ArticlePubMedGoogle Scholar
- Lehmann D, Faber PL, Achermann P, Jeanmonod D, Gianotti LRR, Pizzagalli D. Brain sources of EEG gamma frequency during volitionally meditation-induced, altered states of consciousness, and experience of the self. Psychiatry Res Neuroimaging. 2001;108:111–21.View ArticlePubMedGoogle Scholar
- Barry RJ, Clarke AR, Hajos M, McCarthy R, Selikowitz M, Dupuy FE. Resting-state EEG gamma activity in children with Attention-Deficit/Hyperactivity Disorder. Clin Neurophysiol. 2010;121:1871–7.View ArticlePubMedGoogle Scholar
- Herrmann CS, Demiralp T. Human EEG gamma oscillations in neuropsychiatric disorders. Clin Neurophysiol. 2005;116:2719–33.View ArticlePubMedGoogle Scholar
- Wang Y, Gao X, Hong B, Jia C, Gao S. Brain-Computer Interfaces Based on Visual Evoked Potentials. IEEE Eng Med Biol Mag. 2008;27:64–71.View ArticleGoogle Scholar
- Guger C, Daban S, Sellers E, Holzner C, Krausz G, Carabalona R, Gramatica F, Edlinger G. How many people are able to control a P300-based brain–computer interface (BCI)? Neurosci Lett. 2009;462:94–8.View ArticlePubMedGoogle Scholar
- Eaves DL, Haythornthwaite L, Vogt S (2014) Motor imagery during action observation modulates automatic imitation effects in rhythmical actions. Front Hum Neurosci. doi: 10.3389/fnhum.2014.00028
- Neuper C, Scherer R, Wriessnegger S, Pfurtscheller G. Motor imagery and action observation: Modulation of sensorimotor brain rhythms during mental control of a brain–computer interface. Clin Neurophysiol. 2009;120:239–47.View ArticlePubMedGoogle Scholar
- Mulder T. Motor imagery and action observation: cognitive tools for rehabilitation. J Neural Transm. 2007;114:1265–78.View ArticlePubMedPubMed CentralGoogle Scholar
- Li J, Zhang L. Active training paradigm for motor imagery BCI. Exp Brain Res. 2012;219:245–54.View ArticlePubMedGoogle Scholar
- Ang KK, Guan C, Chua KSG, Ang BT, Kuah CWK, Wang C, Phua KS, Chin ZY, Zhang H. A Large Clinical Study on the Ability of Stroke Patients to Use an EEG-Based Motor Imagery Brain-Computer Interface. Clin EEG Neurosci. 2011;42:253–8.View ArticlePubMedGoogle Scholar
- Birbaumer N, Cohen LG. Brain–computer interfaces: communication and restoration of movement in paralysis. J Physiol. 2007;579:621–36.View ArticlePubMedPubMed CentralGoogle Scholar
- Pfurtscheller G, Muller-Putz GR, Scherer R, Neuper C. Rehabilitation with Brain-Computer Interface Systems. Computer. 2008;41:58–65.View ArticleGoogle Scholar
- Tan D, Nijholt A Brain-Computer Interfaces - Applying our Minds to Human-Computer Interaction.Google Scholar
- Lecuyer A, Lotte F, Reilly RB, Leeb R, Hirose M, Slater M. Brain-Computer Interfaces, Virtual Reality, and Videogames. Computer. 2008;41:66–72.View ArticleGoogle Scholar
- Collinger JL, Wodlinger B, Downey JE, Wang W, Tyler-Kabara EC, Weber DJ, McMorland AJC, Velliste M, Boninger ML, Schwartz AB. High-performance neuroprosthetic control by an individual with tetraplegia. Lancet. 2013;381:557–64.View ArticlePubMedPubMed CentralGoogle Scholar
- Dobkin BH. Brain-computer interface technology as a tool to augment plasticity and outcomes for neurological rehabilitation. J Physiol. 2007;579:637–42.View ArticlePubMedGoogle Scholar
- Prasad G, Herman P, Coyle D, McDonough S, Crosbie J. Applying a brain-computer interface to support motor imagery practice in people with stroke for upper limb recovery: a feasibility study. J NeuroEngineering Rehabil. 2010;7:60.View ArticleGoogle Scholar
- Lledo P-M, Alonso M, Grubb MS. Adult neurogenesis and functional plasticity in neuronal circuits. Nat Rev Neurosci. 2006;7:179–93.View ArticlePubMedGoogle Scholar
- Rossini PM, Calautti C, Pauri F, Baron J-C. Post-stroke plastic reorganisation in the adult brain. Lancet Neurol. 2003;2:493–502.View ArticlePubMedGoogle Scholar
- Garrison KA, Winstein CJ, Aziz-Zadeh L. The Mirror Neuron System: A Neural Substrate for Methods in Stroke Rehabilitation. Neurorehabil Neural Repair. 2010;24:404–12.View ArticlePubMedGoogle Scholar
- Miller KJ, Schalk G, Fetz EE, den Nijs M, Ojemann JG, Rao RPN. Cortical activity during motor execution, motor imagery, and imagery-based online feedback. Proc Natl Acad Sci U S A. 2010;107:4430–5.View ArticlePubMedPubMed CentralGoogle Scholar
- Bermudez i Badia S, Garcia Morgade A, Samaha H, Verschure P. Using a hybrid brain computer interface and virtual reality system to monitor and promote cortical reorganization through motor activity and motor imagery training. Neural Syst Rehabil Eng IEEE Trans On. 2013;21:174–81.View ArticleGoogle Scholar
- Cincotti F, Pichiorri F, Aricò P, Aloise F, Leotta F, de Vico Fallani F, Millán J del R, Molinari M, Mattia D. EEG-based Brain-Computer Interface to support post-stroke motor rehabilitation of the upper limb. Conf Proc IEEE Eng Med Biol Soc. 2012;2012:4112–5.PubMedGoogle Scholar
- Tung SW, Guan C, Ang KK, Phua KS, Wang C, Zhao L, Teo WP, Chew E. Motor imagery BCI for upper limb stroke rehabilitation: An evaluation of the EEG recordings using coherence analysis. Conf Proc IEEE Eng Med Biol Soc. 2013;2013:261–4.PubMedGoogle Scholar
- Pfurtscheller G, Neuper C. Motor imagery and direct brain-computer communication. Proc IEEE. 2001;89:1123–34.View ArticleGoogle Scholar
- McFarland DJ, McCane LM, Wolpaw JR. EEG-based communication and control: short-term role of feedback. IEEE Trans Rehabil Eng. 1998;6:7–11.View ArticlePubMedGoogle Scholar
- Kübler A, Neumann N, Wilhelm B, Hinterberger T, Birbaumer N. Predictability of Brain-Computer Communication. J Psychophysiol. 2004;18:121–9.View ArticleGoogle Scholar
- Cincotti F, Kauhanen L, Aloise F, et al. Vibrotactile Feedback for Brain-Computer Interface Operation. Comput Intell Neurosci. 2007;2007:e48937.View ArticleGoogle Scholar
- Nijboer F, Furdea A, Gunst I, Mellinger J, McFarland DJ, Birbaumer N, Kübler A. An auditory brain-computer interface (BCI). J Neurosci Methods. 2008;167:43–50.View ArticlePubMedGoogle Scholar
- Hinterberger T, Neumann N, Pham M, Kübler A, Grether A, Hofmayer N, Wilhelm B, Flor H, Birbaumer N. A multimodal brain-based feedback and communication system. Exp Brain Res. 2004;154:521–6.View ArticlePubMedGoogle Scholar
- Gomez-Rodriguez M, Peters J, Hill J, Schölkopf B, Gharabaghi A, Grosse-Wentrup M. Closing the sensorimotor loop: haptic feedback facilitates decoding of motor imagery. J Neural Eng. 2011;8:036005.View ArticlePubMedGoogle Scholar
- Hwang H-J, Kwon K, Im C-H. Neurofeedback-based motor imagery training for brain-computer interface (BCI). J Neurosci Methods. 2009;179:150–6.View ArticlePubMedGoogle Scholar
- Lotte F, Larrue F, Mühl C (2013) Flaws in current human training protocols for spontaneous Brain-Computer Interfaces: lessons learned from instructional design. Front Hum Neurosci. doi: 10.3389/fnhum.2013.00568
- Slater M. Place illusion and plausibility can lead to realistic behaviour in immersive virtual environments. Philos Trans R Soc Lond B Biol Sci. 2009;364:3549–57.View ArticlePubMedPubMed CentralGoogle Scholar
- Friedman D, Leeb R, Guger C, Steed A, Pfurtscheller G, Slater M. Navigating Virtual Reality by Thought: What Is It Like? Presence Teleop Virt Environ. 2007;16:100–10.View ArticleGoogle Scholar
- Lotte F (2012) On the need for alternative feedback training approaches for BCI.Google Scholar
- Friedman D. Brain-Computer Interfacing and Virtual Reality. In: Nakatsu R, Rauterberg M, Ciancarini P, editors. Handb. Digit. Games Entertain. Technol. Singapore: Springer; 2015. p. 1–22.View ArticleGoogle Scholar
- Wriessnegger SC, Steyrl D, Koschutnig K, Müller-Putz GR. Short time sports exercise boosts motor imagery patterns: implications of mental practice in rehabilitation programs. Front Hum Neurosci. 2014;8:469.View ArticlePubMedPubMed CentralGoogle Scholar
- Neuper C, Scherer R, Reiner M, Pfurtscheller G. Imagery of motor actions: differential effects of kinesthetic and visual-motor mode of imagery in single-trial EEG. Brain Res Cogn Brain Res. 2005;25:668–77.View ArticlePubMedGoogle Scholar
- Meyer DE, Schvaneveldt RW. Facilitation in recognizing pairs of words: evidence of a dependence between retrieval operations. J Exp Psychol. 1971;90:227–34.View ArticlePubMedGoogle Scholar
- Enhancement of Left-Right Sensorimotor EEG Differences Durin… : Journal of Clinical Neurophysiology. In: LWW. http://journals.lww.com/clinicalneurophys/Fulltext/1999/07000/Enhancement_of_Left_Right_Sensorimotor_EEG.10.aspx. Accessed 18 Nov 2015.
- Garry MI, Kamen G, Nordstrom MA. Hemispheric Differences in the Relationship Between Corticomotor Excitability Changes Following a Fine-Motor Task and Motor Learning. J Neurophysiol. 2004;91:1570–8.View ArticlePubMedGoogle Scholar
- Vourvopoulos A, Cardona JEM, Badia SB i. Optimizing Motor Imagery Neurofeedback through the Use of Multimodal Immersive Virtual Reality and Motor Priming. Valencia, Spain: IEEE, New Jersey, USA; 2015. http://0-ieeexplore.ieee.org.brum.beds.ac.uk/xpl/articleDetails.jsp?reload=true&arnumber=7358592&newsearch=true&queryText=Optimizing%20Motor%20Imagery%20Neurofeedback%20through%20the%20Use%20of%20Multimodal%20Immersive%20Virtual%20Reality%20and#article-page-hdr.
- Kalcher J, Flotzinger D, Neuper C, Gölly S, Pfurtscheller DG. Graz brain-computer interface II: towards communication between humans and computers based on online classification of three different EEG patterns. Med Biol Eng Comput. 1996;34:382–8.View ArticlePubMedGoogle Scholar
- Renard Y, Lotte F, Gibert G, Congedo M, Maby E, Delannoy V, Bertrand O, Lécuyer A. OpenViBE: an open-source software platform to design, test, and use brain-computer interfaces in real and virtual environments. Presence Teleop Virt Environ. 2010;19:35–53.View ArticleGoogle Scholar
- Koles ZJ. The quantitative extraction and topographic mapping of the abnormal components in the clinical EEG. Electroencephalogr Clin Neurophysiol. 1991;79:440–7.View ArticlePubMedGoogle Scholar
- Pfurtscheller G, Guger C, Ramoser H. EEG-based brain-computer interface using subject-specific spatial filters. In: Mira J, Sánchez-Andrés JV, editors. Eng. Appl. Bio-Inspired Artif. Neural Netw. Berlin Heidelberg: Springer; 1999. p. 248–54.View ArticleGoogle Scholar
- Fukunaga K. Introduction to Statistical Pattern Recognition (2Nd Ed.). San Diego, CA, USA: Academic Press Professional, Inc; 1990.Google Scholar
- Vourvopoulos A, Faria AL, Cameirao MS, Bermudez i Badia S. RehabNet: A distributed architecture for motor and cognitive neuro-rehabilitation. In: 2013 IEEE 15th Int. Conf. E-Health Netw. Appl. Serv. Heal. Lisbon, Portugal. 2013. pp 454–459.Google Scholar
- Taylor II RM, Hudson TC, Seeger A, Weber H, Juliano J, Helser AT. VRPN: A Device-independent, Network-transparent VR Peripheral System. In: Proc. ACM Symp. Virtual Real. Softw. Technol. New York: ACM; 2001. p. 55–61.Google Scholar
- Witmer BG, Singer MJ. Measuring Presence in Virtual Environments: A Presence Questionnaire. Presence Teleop Virt Env. 1998;7:225–40.View ArticleGoogle Scholar
- Roberts R, Callow N, Hardy L, Markland D, Bringer J. Movement imagery ability: development and assessment of a revised version of the vividness of movement imagery questionnaire. J Sport Exerc Psychol. 2008;30:200–21.PubMedGoogle Scholar
- Marks DF, Isaac AR. Topographical distribution of EEG activity accompanying visual and motor imagery in vivid and non-vivid imagers. Br J Psychol Lond Engl. 1953;86(Pt 2):271–82.Google Scholar
- Hart SG, Staveland LE (1988) Development of NASA-TLX (Task Load Index): Results of Empirical and Theoretical Research. In: Meshkati PAH and N (ed) Adv. Psychol. North-Holland, pp 139–183. ISBN 978-0-444-70388-0. doi:10.1016/S0166-4115(08)62386-9.
- Delorme A, Makeig S. EEGLAB: an open source toolbox for analysis of single-trial EEG dynamics including independent component analysis. J Neurosci Methods. 2004;134:9–21.View ArticlePubMedGoogle Scholar
- Elliott AC, Woodward WA. Statistical Analysis Quick Reference Guidebook: With SPSS Examples. London, UK: Sage Publications Pvt. Ltd; 2006.Google Scholar
- Whetstone TS (1995) Enhancing Psychomotor Skill Development Through the Use of Mental Practice. J. Ind. Teach. Educ. 32. p5–31.Google Scholar
- Jeannerod M, Frak V. Mental imaging of motor activity in humans. Curr Opin Neurobiol. 1999;9:735–9.View ArticlePubMedGoogle Scholar
- Rizzolatti G, Craighero L. The Mirror-Neuron System. Annu Rev Neurosci. 2004;27:169–92.View ArticlePubMedGoogle Scholar
- Serrien DJ, Sovijärvi-Spapé MM. Hemispheric asymmetries and the control of motor sequences. Behav Brain Res. 2015;283:30–6.View ArticlePubMedGoogle Scholar
- Takeuchi N, Oouchida Y, Izumi S-I, Takeuchi N, Oouchida Y, Izumi S-I. Motor Control and Neural Plasticity through Interhemispheric Interactions, Motor Control and Neural Plasticity through Interhemispheric Interactions. Neural Plast Neural Plast. 2012;2012:e823285.Google Scholar
- Grafton ST, Hazeltine E, Ivry RB. Motor sequence learning with the nondominant left hand. A PET functional imaging study. Exp Brain Res. 2002;146:369–78.View ArticlePubMedGoogle Scholar
- Vaid J, Stiles-Davis J. Mirror writing: an advantage for the left-handed? Brain Lang. 1989;37:616–27.View ArticlePubMedGoogle Scholar
- Pfurtscheller G, Lopes da Silva FH. Event-related EEG/MEG synchronization and desynchronization: basic principles. Clin Neurophysiol. 1999;110:1842–57.View ArticlePubMedGoogle Scholar
- Pfurtscheller G, Berghold A. Patterns of cortical activation during planning of voluntary movement. Electroencephalogr Clin Neurophysiol. 1989;72:250–8.View ArticlePubMedGoogle Scholar
- Pichiorri F, Morone G, Petti M, et al. Brain-computer interface boosts motor imagery practice during stroke recovery. Ann Neurol. 2015;77:851–65.View ArticlePubMedGoogle Scholar
- Malouin F, Richards CL, Jackson PL, Lafleur MF, Durand A, Doyon J. The Kinesthetic and Visual Imagery Questionnaire (KVIQ) for Assessing Motor Imagery in Persons with Physical Disabilities: A Reliability and Construct Validity Study. J Neurol Phys Ther. 2007;31:20–9.View ArticlePubMedGoogle Scholar
- Hamzei F, Läppchen CH, Glauche V, Mader I, Rijntjes M, Weiller C. Functional Plasticity Induced by Mirror Training The Mirror as the Element Connecting Both Hands to One Hemisphere. Neurorehabil Neural Repair. 2012;26:484–96.View ArticlePubMedGoogle Scholar
- Michielsen ME, Selles RW, van der Geest JN, Eckhardt M, Yavuzer G, Stam HJ, Smits M, Ribbers GM, Bussmann JBJ. Motor Recovery and Cortical Reorganization After Mirror Therapy in Chronic Stroke Patients A Phase II Randomized Controlled Trial. Neurorehabil Neural Repair. 2011;25:223–33.View ArticlePubMedGoogle Scholar
- Yavuzer G, Selles R, Sezer N, Sütbeyaz S, Bussmann JB, Köseoğlu F, Atay MB, Stam HJ. Mirror Therapy Improves Hand Function in Subacute Stroke: A Randomized Controlled Trial. Arch Phys Med Rehabil. 2008;89:393–8.View ArticlePubMedGoogle Scholar
- Dohle C, Püllen J, Nakaten A, Küst J, Rietz C, Karbe H. Mirror Therapy Promotes Recovery From Severe Hemiparesis: A Randomized Controlled Trial. Neurorehabil Neural Repair. 2009;23:209–17.View ArticlePubMedGoogle Scholar