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Technical Correspondence
Myoelectric Pattern Recognition Based on Muscle Synergies for
Simultaneous Control of Dexterous Finger Movements
Shenquan Zhang, Xu Zhang, Shuai Cao, Xiaoping Gao, Xiang Chen, and Ping Zhou

Abstract—Motor activities during daily life always involve simultaneous of freedom (DOFs) for multifunctional use [4], especially for con-
control of multiple degrees of freedom (DOFs), which has not yet been trolling dexterous hand or finger movements [5], [6]. State-of-the-art
fully explored in myoelectric control due to difficulty in sufficiently decod-
ing the complex neural control information. This study presents a novel myoelectric controllers have been reported to support the control of
framework for simultaneous myoelectric control based on pattern recog- more than 4 DOFs in total [5]–[8]. However, one main limitation of
nition incorporated with a muscle synergy motor control strategy for each the pattern-recognition-based control strategy is its sequential selection
DOF. An experiment for discriminating 18 dexterous finger movement of different DOFs or task patterns. This contrasts sharply with natu-
tasks was designed to evaluate the performance of the framework for the
simultaneous control of 5 DOFs. Task discrimination was assessed with 18
ral motor control, which is based on simultaneous control of multiple
neurologically intact subjects, and the framework exhibited high accuracy DOFs [7].
(96.79% ±2.46%), outperforming three other methods, including the rou- Many studies have recently been conducted on simultaneous control,
tine myoelectric pattern-recognition approach for conventional sequential and some have reported promising results [9], [10]. The concept of mus-
control (p<0.001). Furthermore, the feasibility of the proposed framework cle synergy has been employed in myoelectric control methods by many
is also demonstrated with data from paretic muscles of two stroke subjects.
This study offers a feasible solution for simultaneous myoelectric control recent studies to decode neural control information. Muscle synergy is
of multiple DOFs, which has great potential for natural implementation in mathematically described as a vector that specifies a pattern of relative
prosthetic hand devices and robotic training systems, especially for dexter- muscle activation with activation coefficients related to the strength of
ous finger movements. motor drive from the central nervous system [11]. Any complex move-
Index Terms—Myoelectric pattern recognition, muscle synergy, ments can be formulated by multiple weighted combinations of muscle
simultaneous control, stroke rehabilitation. synergies. Inspired by this idea, Jiang et al. made many achievements
in extracting simultaneous control information from surface EMG [9].
Ison and Artemiadis [11] also showed that muscle synergies extracted
I. INTRODUCTION from EMG can be used to promote intuitive myoelectric control.
Although enormous progress has been made in the simultaneous con-

M YOELECTRIC control is a technique that enables interpreta-


tion of movements or movement intentions as control com-
mands by recording and processing surface electromyography (EMG).
trol of multiple DOFs in recent years, the number of simultaneously
activated DOFs is still limited to three [9]–[12]. A generative model
proposed by Jiang et al. [9] managed to control two DOFs simultane-
The method has been widely used in prosthetic control since the 1960s ously, but it turned out to be invalid when an additional third DOF was
[1], and it is used more generally as an input interface for human- included. Young et al. [12] reported a 4-DOF control approach under
computer interaction [2], [3]. Myoelectric pattern recognition has been the restriction that no more than 2 DOFs would be activated at the
developed as a useful strategy to enable control of multiple degrees same time. Recent efforts on simultaneous myoelectric control have
always involved upper-limb gross motor activities, such as hand clos-
ing/opening and extension/flexion of the wrist and elbow [9], [10], [12].
Investigations into simultaneous control of dexterous finger movements
Manuscript received September 1, 2016; revised January 10, 2017; accepted remain insufficient due to the challenge that at least 5 DOFs need to be
March 25, 2017. This work was supported in part by the National Natural decoded simultaneously.
Science Foundation of China under Grant 61401421 and Grant 61431017, and
in part by the Fundamental Research Funds for the Central Universities under In this paper, a novel framework for myoelectric simultaneous con-
Grant WK2100230014. This paper was recommended by Associate Editor X. trol of multiple DOFs is proposed to discriminate dexterous finger
Hu. (Corresponding author: Xu Zhang.) movements. The activities of five fingers are processed separately to
S. Zhang, X. Zhang, S. Cao, and X. Chen are with the Department of control 5 DOFs, and the control of each DOF relies on myoelectric pat-
Electronic Science and Technology, University of Science and Technology of
tern recognition incorporated with muscle synergies specific to the ac-
China, Hefei 230027, China (e-mail: zsq350@mail.ustc.edu.cn; xuzhang90@
ustc.edu.cn; caoshuai@mail.ustc.edu.cn; xch@ustc.edu.cn). tivities of the corresponding finger. Surface EMG signals are recorded
X. Gao is with the Department of Rehabilitation Medicine, First Affil- via two flexible high-density electrode arrays placed over both fin-
iated Hospital of Anhui Medical University, Hefei 230022, China (e-mail: ger extensors and flexors around the forearm. The discrimination of
gxp678@163.com). 18 tasks involving activities of any single finger or different finger
P. Zhou is with the Guangdong Work Injury Rehabilitation Center, Guangzhou
510440, China, and also with the Department of Physical Medicine and combinations was conducted to evaluate the performance of the pro-
Rehabilitation, University of Texas Health Science Center at Houston, and posed framework.
TIRR Memorial Hermann Research Center, Houston, TX 77030 USA (e-mail: This study is a part of our continuous efforts to explore the
ping.zhou.1@uth.tmc.edu). application of myoelectric pattern recognition for neurological injury
Color versions of one or more of the figures in this paper are available online
patients (such as stroke, spinal cord injury, and cerebral palsy patients)
at http://ieeexplore.ieee.org.
Digital Object Identifier 10.1109/THMS.2017.2700444 [13]–[15]. The results of the current study could not only benefit

2168-2291 © 2017 IEEE. Personal use is permitted, but republication/redistribution requires IEEE permission.
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2 IEEE TRANSACTIONS ON HUMAN-MACHINE SYSTEMS

Fig. 2. Illustration of the 18 finger movement tasks.

a 4 × 8 matrix. Each recording probe had a diameter of 3 mm, and the


center-to-center distance between two consecutive probes was 10 mm.
When placed over the forearm, both arrays constituted an entire array
in a 4 × 16 matrix, producing a total of 64 channels of EMG recordings
in a monopolar configuration. The second row of the entire array was
aligned around the maximal circumference around the forearm. A round
Fig. 1. Electrode placement for 64-channel surface EMG signal recording
using two pieces of flexible high-density electrode arrays placed over both the reference electrode was located on the olecranon of the same arm.
posterior and anterior sides of the forearm. The numbers in circles represent To facilitate signal collection during the experiment, a wide stretch-
indices of surface EMG channels. The uppercase letters and lowercase letters able nylon belt was used as an armband over the electrode arrays to
denote the indices of rows and columns of the entire electrode array, respectively. prevent loose connections between the recording probes and the skin
surface. The surface EMG signals were recorded by a custom-made data
prosthetic users, but also advance dexterous robotic training for recording system capable of recording up to 128 channels at the same
neurological injury patients driven by simultaneous control of multiple time. Each surface EMG channel was processed by a two-stage ampli-
DOFs, which may have better therapeutic effects than passive training fier with a total gain of 60 dB, a built-in band-pass filter (20–500 Hz),
or simple active training driven by conventional myoelectric control and digitalization at a sampling rate of 1000 Hz. The recorded data
[15]. The framework was tested on both neurologically intact subjects were transferred and stored on a computer via USB cable. A software
and hemiparetic stroke survivors. package was also developed to monitor all the recorded EMG data on
the computer screen in real time.
II. METHODS
C. Experimental Protocol
A. Subjects
In the experiment, subjects were comfortably seated in a chair, and
Participants in the data collection experiment comprised 18 neuro- their dominant arm was placed over a height-adjustable side table for
logically intact subjects (all male, 16 right-handed and 2 left-handed, the test with shoulder abduction at 30°, elbow flexion at 90°, and slight
age 21–27 years) and two stroke subjects (both male, 45 and 54 years wrist pronation to allow the hand to be placed flat on the horizontal
old, both right-handed before stroke, 1 and 2 months since the on- surface of the table. The subject was instructed to perform 18 gesture
set of stroke, denoted as S1 and S2). The experiment was approved by tasks involving the extension of different individual fingers or finger
the institutional ethics review board. The stroke survivors suffered from combinations, as shown in Fig. 2. The experiment protocol comprised
substantial hemiplegia on the right side of the body after either cerebral 18 trials. For each trial of the same task, the subject was guided by
infarction or cerebral hemorrhage. Their hand motor function scored an experimenter to start or terminate each of five repetitions in total.
58 and 38 on the upper-extremity component of the Fugl–Meyer scale The subject was required to perform (or intend to perform, especially
(a total score of 66 represents full function) [16] and 5 and 2 on the for both stroke subjects following substantial hemiparesis) a muscle
hand impairment part of the Chedoke–McMaster stroke assessment contraction with a mild to moderate force that just enables the activities
scale (a full score of 7 represents full function) [17]. There was no of specific fingers to be activated and maintained and to hold the task
requirement for stroke subjects to be able to perform the tested tasks for approximately 3 s. A sufficiently long rest period was allowed for
using the affected hand. Written consent was obtained from all subjects each subject between consecutive trials and repetitions to avoid muscle
before the experiment. fatigue.

B. Data Acquisition D. Data Segmentation and Feature Extraction


The data acquisition experiment was performed on the dominant- The recorded EMG data showed five activity bursts corresponding
hand side of all neurologically intact subjects and the hemiparetic side to five repetitions of each movement in one trial. Both the onset and
of both stroke subjects. Fig. 1 illustrates the placement of electrodes offset times of each repetition were straightforwardly determined using
over the right hand as an example. Two flexible high-density electrode a routine amplitude-thresholding approach [18]. Each detected data
arrays were used to collect surface EMG data from finger extensors and segment corresponding to one repetition was further segmented into a
flexors on mainly the posterior and anterior sides around the forearm, series of overlapped analysis windows with a window size of 256 ms
respectively. Each array consisted of 32 recording probes arranged in and a window increment of 32 ms. These analysis windows were also
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IEEE TRANSACTIONS ON HUMAN-MACHINE SYSTEMS 3

considered as basic data samples in the feature extraction and pattern the Euclidean distance between v and v̂p . In the synergy-based EMG
classification analyses. classification, the distance was quite small when the data sample truly
The Hudgins’ feature set [4], [13] was used to extract four time- belonged to the pattern considered (positive in this case). Therefore, it
domain (TD) parameters: the mean absolute value (MAV), wave- is reasonable to make the decision about the DOF by comparing the
form length (WL), number of zero-crossings (ZC), and number of distance with a predefined threshold. The DOF is positive if the distance
slope sign changes (SSC) from each EMG channel. This produced a is smaller than the threshold, and negative otherwise. The threshold
256-dimensional (4 × 64) feature vector for each data sample. The was determined based on the maximum classification accuracy with
reasons for adopting the TD feature set included its reported effective- the training dataset. Generally, these thresholds varied across DOFs.
ness in EMG pattern recognition and low computational complexity. 2) Pattern Comparison Version of MSD for Simultaneous
Another reason was its nonnegative definition, which is very important Control (MSDSC-2): MSDSC-2 applies the same procedure as
for the muscle synergy analysis [19], [20]. The features from all data MSDSC-1 to the negative pattern as well. In the training phase, the
samples were further normalized to a range between 0 and 1 using the training dataset Vn t r n was additionally formed and further decom-
min–max normalization [21]. posed via (1) to obtain Wn for the negative pattern. In the testing
phase, given an unknown testing sample v, two distance values dp
E. Muscle Synergy Analysis and dn were computed accordingly for both the positive and nega-
tive patterns. The lower distance indicated higher likelihood that the
The muscle synergy model used in this paper is described as: data sample belonged to the corresponding pattern. Thus, the main
difference of this method from MSDSC-1 is replacing the threshold
V m ×n = Wm ×r × Hr ×n (1)
by dn ; that is, the state is positive if dp is lower than dn , and negative
where Vm ×n denotes a group of n data samples (each represented in otherwise.
an m-dimensional feature vector) arranged in a matrix form, W and In muscle synergy analysis, the number of muscle synergies is a cru-
H denote the synergy matrix and the activation coefficient matrix, cial parameter that might affect the classification performance. A small
respectively, and r(< m) is the number of extracted synergies. Given synergy number might not carry sufficient information, while one that
V , the problem of determining both W and H is a typical blind source is too large would increase the calculation burden and even compro-
separation problem. This problem was solved using nonnegative matrix mise the performance. Therefore, the synergy number was varied from
factorization due to its effectiveness in extracting muscle synergies [22]. 3 to 25 to examine its effect on the classification performance using
both methods.
F. Synergy-Based Classification for Simultaneous Control
All the examined tasks were regarded to be performed via five inde- G. Performance Evaluation
pendent DOFs corresponding to activities of the five fingers. For each The task discrimination was conducted in a user-specific manner.
DOF, there are positive and negative states representing whether or not Given five repetitions of each task during the data collection, a five-
the corresponding finger is extended. Therefore, the proposed frame- fold cross-validation testing scheme was used to use the data efficiently.
work involved simultaneously identifying the states of five DOFs to The EMG data within any four repetitions were selected and assigned
make a final decision for task discrimination. Within this framework, a for training classifiers, and the remaining EMG data were referred to
classification approach incorporated with muscle synergy information as the testing dataset. To quantify the classification performance, the
was implemented as a classifier for each DOF. overall accuracy was defined by calculating the percentage ratio of the
Fig. 3 shows block diagrams of both the proposed simultaneous con- number of correctly identified data samples to the number of all data
trol framework and the synergy-based classifier for each DOF. Given samples over five testing trials in total for each subject.
a set of synergies specific to a movement task, whether an unknown A linear discriminant classifier (LDC) was employed for perfor-
data sample belongs to that task can be validated by how accurately the mance comparison. The LDC involves a linear discriminant analysis
encoding process can simulate the sample with those synergies. This (LDA) to enhance the class separability. A subsequent linear classifier
is regarded as the fundamental principle of the task-specific muscle- models the within-class density of each class as a multivariant Gaus-
synergy-based discrimination (MSD) method proposed by Rasool et sian distribution and gives decisions about unknown samples based on
al. for EMG classification [23]. Accordingly, two versions of the MSD maximum a posterior Bayesian estimation [13]. Specifically, a multi-
method were implemented as classifiers at the individual DOF level, variate extension of LDA called uncorrected LDA [24] was adopted
thus producing two methods for simultaneous control in the current due to the high dimension of feature vectors derived from high-density
study. surface EMG recordings. We implemented the LDC in two different
1) Threshold-Based Version of MSD for Simultaneous Con- schemes. In one scheme, the LDC is embedded in the proposed simul-
trol (MSDSC-1): When a single DOF was considered, movement taneous control framework (LDCSC) and works as a classifier at the
tasks were categorized by the positive and negative states into two pat- individual DOF level. The other allows us the LDC to work on TD fea-
terns: a positive pattern consisting of all tasks involving extension of tures directly, thus enabling conventional sequential control. The latter
the finger corresponding to the considered DOF, and a negative pat- scheme (LDC) has been adopted as a routine solution to myoelectric
tern consisting of other tasks. In the training phase as shown in Fig. pattern recognition with many successful applications [4], [5], [13].
3, the training dataset Vp t r n consists of data samples from all tasks Without the simultaneous control capability, LDC was used as a base-
belonging to the positive pattern. Muscle synergy analysis was then line for evaluating the task discrimination accuracy between different
performed on Vp t r n via (1) to obtain a synergy matrix Wp specific to methods.
the positive pattern. Two one-way repeated-measure analyses of variance (ANOVAs)
In the testing phase, given the constant Wp , an unknown testing were applied to the overall accuracy obtained from 18 neurologically
sample v was factorized to estimate the activation coefficient ĥp . The intact subjects using both MSDSC-1 and MSDSC-2 methods to deter-
reconstructed version of v was denoted as v̂p , which was calculated mine the appropriate synergy number (considered as the within-subject
as v̂p = Wp × ĥp . Next, the reconstruction residual was computed as factor ranging from 3 to 25). Another one-way repeated-measure
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4 IEEE TRANSACTIONS ON HUMAN-MACHINE SYSTEMS

Fig. 3. (a) Flowchart of the proposed framework for simultaneous myoelectric control of five DOFs. (b) Two versions of the muscle synergy-based myoelectric
pattern classifier implemented at each DOF level for simultaneous control (MSDSC-1 and MSDSC-2).

rapidly to 67.38 ± 10.53% for the MSDSC-1 and 96.79 ± 2.45% for the
MSDSC-2. Further increase in the synergy number beyond 11 did not
obviously improve the mean accuracies, which remained stable around
68% and 98% for the respective methods. The ANOVAs confirmed
that there was no significant difference in the accuracy for the synergy
number of 11 versus any larger numbers (p > 0.3). Thus, the synergy
number was optimally set to 11 in the following analysis.

B. Characterization of Muscle Synergies


Given the spatial EMG activity recorded by two-dimensional elec-
trode arrays, each derived muscle synergy could be characterized by a
contour plot, where only one feature was used for each EMG channel,
and its value was represented by different colors. Fig. 5 shows exam-
Fig. 4. Effect of synergy number on recognition accuracy using both MSDSC ples of the EMG MAV feature contour plots for both the positive and
methods. The accuracies are averaged across 18 neurologically intact subjects negative patterns of DOF 1 from a representative subject. The left panel
and plotted with SD error bars.
of Fig. 5 shows the contour plots of all derived muscle synergies and
their direct summations for both positive and negative patterns for a
ANOVA was applied to the overall accuracy with the classification synergy number of 6. Surprisingly, we also found that such a synergy
method (MSDSC-1, MSDSC-2, LDCSC, and LDC) considered as summation kept almost a constant pattern when varying values of the
within-subject factors. Post hoc pairwise multiple comparisons with synergy number, as shown in the right panel of Fig. 5.
Bonferroni correction were used when necessary. The level of statis- The individual synergies were likely to appear in distinct contour
tical significance was set to p < 0.05 for all analyses. A prior power plots at different synergy numbers, but their summations offered a
analysis for the ANOVA was conducted to test the sample size using straightforward way of characterizing each DOF pattern. Therefore,
PASS software (ver. 11.0, NASS LLC. Kaysville, UT), while all other Fig. 6 shows contour plots of synergy summations for both patterns
statistical analyses were completed using SPSS software (ver. 16.0, of all five DOFs at a synergy number of 11. Based on the muscle
SPSS Inc. Chicago, IL). synergy summation, each DOF showed distinct positive and negative
patterns. The contour plots in this case were based on only MAV, an
amplitude-associated EMG feature, but more features were extracted in
III. RESULTS the following pattern recognition, including MAV, WL, ZC, and SSC.
A. Synergy Number Determination
C. Classification Results for Simultaneous Control
Fig. 4 shows the effect of synergy number on recognition accuracy
averaged across 18 neurologically intact subjects using both MSDSC-1 With the synergy number set to 11, myoelectric pattern recogni-
and MSDSC-2 methods. A very small synergy number led to relatively tion analyses were performed using the two proposed MSDSC meth-
low accuracies for both methods. When the synergy number was in- ods. Fig. 7 shows the classification accuracies averaged across all
creased from 3 to 11, the mean accuracy across all subjects increased 18 neurologically intact subjects. MSDSC-2 outperformed MSDSC-1
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Fig. 5. Examples of the muscle synergy contour plots measured by a MAV feature (units of µV) of surface EMG for both the positive and negative patterns of
DOF 1 from one representative subject (Subject 1). The left panel shows contour plots of all individual muscle synergies and their direct summations when the
synergy number was set to 6. The right panel shows all these synergy summations for both patterns when the synergy number was set to 1, 3, 5, 7, 9, 10, and 11,
respectively. The summation is equal to the sole synergy at the synergy number of 1.

Fig. 6. Muscle synergy summations for both positive and negative patterns of
all five DOFs when the synergy number was set to 11.

Fig. 7. Average classification accuracies across all 18 neurologically intact


subjects for identifying two patterns of five individual DOFs and for discrimi-
nating all 18 finger movement tasks using MSDSC-1, MSDSC-2, and LDCSC
and LDCSC in both DOF pattern identification and task discrimina- methods, respectively. The error bars indicate standard deviations.
tion. The accuracy for final task discrimination was also lower than
that for DOF pattern identification due to the stronger criterion where
the correctness of the final task discrimination relied on simultaneous 81.09%, 59.04%, and 86.87% for subject S2 for MSDSC-1, MSDSC-2,
correctness of five decisions of all DOFs. LDCSC, and LDC, respectively.
Fig. 8 shows the overall classification accuracies for 18 neurologi-
cally intact subjects and two stroke subjects, where only the mean accu-
IV. DISCUSSION
racies averaged over all neurological intact subjects were reported with
standard deviations. With the neurologically intact data, MSDSC-2 had Simultaneous myoelectric control of multiple DOFs could provide
a high mean accuracy of 96.79 ± 2.46%, whereas that for MSDSC-1 a practical way of developing advanced muscle-computer interfaces.
was only 67.38 ± 10.53%. The LDCSC and LDC achieved mean accu- This study proposes a novel framework for simultaneous control of
racies of 87.36% ± 4.11% and 91.66% ± 5.66%, respectively. Pairwise 5 DOFs using muscle-synergy-based EMG pattern recognition at the
comparisons in ANOVA further indicated that there was a significant individual DOF level. The promising classification results validated
difference (p < 0.001) in overall accuracy between any two pairs of the effectiveness of the proposed method. Moreover, when testing on a
classification methods. This shows that the proposed MSDSC-2 method common PC with a 3.4-GHz Core i3 CPU and 4GB RAM, we calculated
outperformed the other three approaches across neurologically intact a time delay of about 7 ms for processing a 256-ms analysis window
subjects. With the stroke data, the overall accuracies were 44.58%, using either of the MSDSC methods. This demonstrates the computa-
81.81%, 72.96%, and 82.16% for subject S1, while they were 26.26%, tional efficiency of the proposed method for realizing real-time control
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6 IEEE TRANSACTIONS ON HUMAN-MACHINE SYSTEMS

5% (p < 0.001). Moreover, the superior performance of MSDSC-2 over


LDCSC indicated the advantage of using the muscle-synergy-based
approach as a DOF classifier for simultaneous control.
Both stroke subjects had obviously lower classification accuracies
than the accuracies averaged across neurologically intact subjects, re-
gardless of the classification method. Such performance degradation
has been reported consistently by many previous studies [13]–[15] and
is probably due to the affected delivery of neural control information
in paretic muscles following stroke. However, among the three ap-
proaches supporting simultaneous control, the MSDSC-2 achieved the
highest accuracy for both stroke subjects. High accuracy over 80%
could potentially guarantee the implementation of simultaneous my-
oelectric control devices for advanced robotic training, which would
enable stroke subjects to perform dexterous movements voluntarily
Fig. 8. Classification accuracies for all neurologically intact subjects and toward enhanced functional restoration. Although the LDC method
stroke subjects S1, S2 using tested classification methods.
yielded comparable or even slightly higher accuracies, it worked in
the manner of a conventional sequential control without simultaneous
control capability.
systems. The proposed method offers a feasible solution for simultane- The main limitation of the current study is that only the OFFLINE
ous control of multiple DOFs, which would not only benefit prosthetic classification was presented without an evaluation of real-time con-
users but also has potential applications in stroke rehabilitation. trollability. Based on the very preliminary test on the processing
Increasing the synergy number from 3 to 11 led to dramatic improve- delay in the current study, it should be acknowledged that the pro-
ment in average accuracy from 70% to approximately 97%, but further posed framework is computationally efficient and fully compatible
increases did not change the performance much. This indicates that a with real-time applications. Our future work focuses on actual imple-
limited number of muscle synergies may be sufficient to characterize mentation of the proposed simultaneous myoelectric control devices,
complex functional tasks. This finding is consistent with a previous especially for dexterous hand robotic training towards enhanced stroke
study reporting that eight synergies could account for at least 90% of rehabilitation.
the variance of all myoelectric patterns of hand postures [19]. Based
on the tradeoff between classification performance and computational V. CONCLUSION
burden, the synergy number was set to 11 in this study.
The use of a high-density surface EMG electrode array has proven We presented a novel framework for simultaneous myoelectric con-
to offer a great opportunity to record valuable spatial information about trol of multiple DOFs by implementing myoelectric pattern recogni-
muscular activities [13]. Given such spatial information, the processed tion based on the muscle synergies at each DOF level. The feasibility
muscle synergies can be visualized in the form of contour plots, as of the framework was demonstrated by discriminating 18 hand ges-
shown in Figs. 5 and 6. Although the resultant muscle synergies were tures involving dexterous finger movements, where an individual fin-
likely to vary with different synergy numbers, quite surprisingly, the ger corresponds to one DOF. The proposed framework (particularly
contour plots of the summation of all the decomposed muscle synergies the MSDSC-2 method) outperformed the other methods in terms of
remained almost constant (see Fig. 5). Therefore, it was straightforward the average accuracy from 18 neurologically intact test subjects (p <
to compare the muscle synergies derived from different DOF patterns 0.001). The method was also demonstrated with data from hemiparetic
by the contour plots of their summations. Specific to each DOF state, stroke subjects. The framework is a feasible solution for simultaneous
the muscle synergy summation over the forearm muscles had a distinct myoelectric control of multiple DOFs with potential applications in
pattern (see Fig. 6), which demonstrated the fundamental feasibility of driving dexterous hand/finger prosthetic devices or robotic training.
performing synergy-based myoelectric classification at the individual
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IEEE TRANSACTIONS ON HUMAN-MACHINE SYSTEMS 7

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