Sensors 19 03309
Sensors 19 03309
Article
Development of an EMG-Based Muscle Health Model
for Elbow Trauma Patients
Emma Farago 1 , Shrikant Chinchalkar 2 , Daniel J. Lizotte 3,4 and Ana Luisa Trejos 1,5, *
1 Department of Electrical and Computer Engineering, Western University, London, ON N6A 5B9, Canada
2 Division of Hand Therapy, Hand and Upper Limb Centre, St. Joseph’s Health Care, London, ON N5V 3A1,
Canada
3 Department of Computer Science, Western University, London, ON N6A 5B9, Canada
4 Department of Epidemiology & Biostatistics, Western University, London, ON N6A 5B9, Canada
5 School of Biomedical Engineering, Western University, London, ON N6A 5A5, Canada
* Correspondence: [email protected]; Tel.: +1-519-661-2111 (ext. 89281)
Received: 10 June 2019; Accepted: 25 July 2019; Published: 27 July 2019
Abstract: Wearable robotic braces have the potential to improve rehabilitative therapies for patients
suffering from musculoskeletal (MSK) conditions. Ideally, a quantitative assessment of health would
be incorporated into rehabilitative devices to monitor patient recovery. The purpose of this work is
to develop a model to distinguish between the healthy and injured arms of elbow trauma patients
based on electromyography (EMG) data. Surface EMG recordings were collected from the healthy
and injured limbs of 30 elbow trauma patients while performing 10 upper-limb motions. Forty-two
features and five feature sets were extracted from the data. Feature selection was performed to
improve the class separation and to reduce the computational complexity of the feature sets. The
following classifiers were tested: linear discriminant analysis (LDA), support vector machine (SVM),
and random forest (RF). The classifiers were used to distinguish between two levels of health: healthy
and injured (50% baseline accuracy rate). Maximum fractal length (MFL), myopulse percentage
rate (MYOP), power spectrum ratio (PSR) and spike shape analysis features were identified as the
best features for classifying elbow muscle health. A majority vote of the LDA classification models
provided a cross-validation accuracy of 82.1%. The work described in this paper indicates that it is
possible to discern between healthy and injured limbs of patients with MSK elbow injuries. Further
assessment and optimization could improve the consistency and accuracy of the classification models.
This work is the first of its kind to identify EMG metrics for muscle health assessment by wearable
rehabilitative devices.
1. Introduction
Musculoskeletal (MSK) conditions are disorders or injuries that affect the bones, joints, skeletal
muscles and/or connective tissues. Without adequate rehabilitation, MSK injuries could become
chronic as a result of joint stiffness and reduced muscle strength [1].
The development of lightweight robotic braces offers a potential for improved rehabilitation.
Wearable rehabilitation robotic devices have been successful in improving rehabilitation program
compliance, accelerating recovery, and monitoring health for patients suffering from neuromuscular
damage from stroke [2]. Mechatronic braces for patients with neurological disorders have been
developed to assist with mobility and to allow patients to perform exercises at home and at their
own convenience [3]. However, there has been little work done to develop rehabilitation devices for
patients with MSK injuries, in which damage affects the bones, muscles, and connective tissues, but in
which the central nervous system is intact.
The rehabilitation of the elbow following trauma is an inherently challenging process due to the
complexity of the elbow joint [4]. Inadequate rehabilitation leads to the development of stiff elbow
and a loss of range of motion (ROM) [5]. Rehabilitation following elbow trauma should involve
passive and active ROM exercises to ensure that the ensuing collagen remodeling and elongation of the
tendinous and capsular tissues allow for joint motion. ROM exercises typically involve elbow flexion
and extension, and forearm pronation performed with the elbow at 90 degrees [4].
Most of the scientific evidence to support certain rehabilitation approaches is based on
retrospective and case series studies with small sample sizes, not on randomized clinical trials
(RCTs) [5], and the optimum dosage of the frequency and repetition of ROM exercises is unknown [4,5].
Furthermore, the rehabilitative procedures tested are often poorly described and not reproducible [5],
and the outcome measures often depend on the therapist’s perspective [6]. Measurements from smart
wearable devices could improve the objectivity of muscle health assessment, and lead towards stronger
evidence-based rehabilitation.
An ideal rehabilitative smart device would be capable of objectively and autonomously
determining a patient’s muscle health. This would enable a path towards (1) improved diagnostics,
(2) the development of individualized therapies specific to a patient’s level of health, and (3) the
identification of objective outcome measures to inform evidence-based rehabilitation practices.
Electromyography (EMG), the study of the electrical currents generated during muscle contraction,
offers a possible solution for assessing muscle health with a smart brace. EMG signals can be collected
directly from muscle units by inserting a needle into the muscle fiber. Surface EMG (sEMG) signals are
collected noninvasively by placing electrodes on the surface of the skin. Quantitative EMG analysis is
an established diagnostic tool for patients with nerve damage and skeletal muscle damage.
A range of models including artificial neural networks, support vector machines, and decision
trees have been used to successfully classify needle EMG signals as neuropathic, myopathic, or
normal [7,8]. There is some evidence that sEMG data from patients with elbow injuries conform to
patterns that distinguish the level of injury and could therefore be used to quantify the success of a
therapy. Patients with elbow motion deficits following injury have been observed to have increased
sEMG activity in their elbow muscles during elbow flexion and extension compared to controls [9].
However, there is no classification method that can be implemented in an elbow rehabilitation device to
monitor and assess patient health following elbow trauma. If these differences could be modeled using
a classification system, they could be implemented in a rehabilitative robotic device and a patient’s
health could be monitored as they progress through the rehabilitation process.
As a first step in this direction, this paper investigates methods of using sEMG data for classifying
upper limbs as healthy or injured. The remainder of the paper is organized as follows: Section 2
provides background information about feature extraction for sEMG signal classification. Section 3
explains the methods used in the study, including data collection, feature extraction, feature selection,
and classification. Section 4 describes the classification results, Section 5 is the discussion, and Section 6
provides the conclusions.
2. Background
EMG data are typically classified using pattern recognition techniques [10]. Following
EMG acquisition, the data are windowed into segments, and features are extracted from each
segment. Feature extraction allows useful information to be obtained from the sEMG signal, and
reduces unwanted information and noise [11]. Numerous features have been proposed for sEMG
classification [12,13]. The features used in this study are summarized in Table 1.
Sensors 2019, 19, 3309 3 of 15
Table 1. List of common sEMG features with references. K is the number of window segments used for
multi-window features.
Entropy Features
The approximate entropy (ApEn) feature is a measure of system complexity used to classify
stochastic processes [16]. ApEn has been applied to sEMG signals for motion classification [22].
ApEn represents the likelihood that similar patterns of observations will not be followed by similar
observations. The sample entropy (SampleEn) feature is a refinement of ApEn that improves the
consistency of comparisons between data sets [19].
features. The RMS and MAV features collected from the patients at the end of the therapy program
were found to resemble the healthy population more closely. The frequency domain features, MDF
and MNF, showed no significant differences between the groups.
2.3. Classification
Following feature extraction, machine learning classifiers (including linear discriminant analysis
(LDA), support vector machines (SVM), and decision tree classifiers) are applied to the extracted
features to classify the EMG data. LDA is a robust classifier and is advantageous for embedded
processors involved with real-time applications because it provides fast prediction speeds and small
memory usages. LDA has been applied to a variety of EMG classification problems [26], and is generally
found to provide acceptable classification accuracies [20]. An extension of the LDA classification
method is the SVM classifier, which uses separating hyperplanes to distinguish between two classes of
data. The SVM classifier has been used for many EMG applications including motion classification [15]
and the diagnosis of neuromuscular disorders [27].
LDA and linear SVM models may perform poorly if the relationships between features are
non-linear. Decision tree classifiers are simple models that provide easily interpretable results, and can
outperform linear models when classifying non-linear data. A single decision tree classifier determines
an outcome based on a series of splitting rules starting at the top of a tree and continuing into a series
of branches. The decision tree stratifies the feature space into regions to provide the prediction. A
single decision tree model is susceptible to over-fitting and a lack of robustness. These problems can
be avoided by aggregating many decision trees. The random forest (RF) algorithm prevents decision
tree models from considering most of the available predictors at each split [28].
2.4. Summary
Pattern recognition techniques have been applied to the classification of sEMG signals by
motion [13,29], force [30], neuromuscular health [7], and fatigue [31,32]. There has not been a
study, however, classifying muscular health of patients following MSK injury, although preliminary
evidence suggests that muscle activation patterns differ between healthy and injured patients [25]. This
paper investigates the application of sEMG features to the classification of muscle health following
MSK injury.
3. Methods
Working from the sEMG features presented above, this section now describes the methods of
data collection and data analysis (feature extraction, feature selection, classification, evaluation, and
optimization) with the objective of identifying and assessing the ability of features to distinguish elbow
muscle health.
extensor carpi ulnaris (ECU), and flexor carpi ulnaris (FCU). Electrodes were placed according to the
SENIAM recommendations for electrode placement [33].
All sEMG signals were collected and amplified with a commercial wireless myoelectric system
(Trigno Wireless system, Delsys Inc., Natick, MA, USA). The signals were amplified with a gain of
300×, and the sampling frequency was 1925.93 Hz. The sensors were affixed to the skin using the
recommended double-sided adhesive stickers (Trigno Sensor Skin Interface SC–F03).
Patients were asked to perform three repetitions of the following motions with both the injured
and the contralateral uninjured arm: elbow flexion (EF), elbow extension (EE), forearm pronation
(P), forearm supination (S), wrist flexion (WF), wrist extension (WE), ulnar deviation (UD), radial
deviation (RD), hand open (HO), and hand close (HC). Motions were selected based on standard elbow
rehabilitation exercises. Wrist and hand exercises were included because elbow trauma patients are
also encouraged to perform wrist and finger exercises during rehabilitation [4]. The forearm, wrist,
and hand exercises were performed with the elbow held at approximately 90 degrees (Figure 1).
Figure 1. Ten upper-limb motions performed: (a) elbow flexion (EF), (b) elbow extension (EE),
(c) forearm pronation (P), (d) forearm supination (S), (e) wrist flexion (WF), (f) wrist extension (WE),
(g) ulnar deviation (UD), (h) radial deviation (RD), (i) hand open (HO), and (j) hand close (HC).
Motions were performed in sets with the patient pausing at the end of each motion. The following
order of motion sets was used for every trial: EF/EE, P/S, WF/WE, UD/RD, and HO/HC. Each
motion set was performed with the injured arm three times, and then with the uninjured arm three
times. The forearm, wrist, and hand exercises were performed with the elbow at approximately
90 degrees. The patients were instructed to perform all motions at a comfortable pace.
The segmentations for each sEMG recording were verified visually and sets that were not
segmented correctly by the algorithm were segmented manually. About 50% of the data sets had to be
resegmented manually. Data sets from three subjects were excluded from further analysis after visual
inspection indicated that the data were corrupted.
The sEMG signals were filtered with a 2nd order Butterworth 20–400 Hz band pass filter to
remove low frequency motion artifacts, and uninformative high-frequency components. The signals
were also filtered with a 60 Hz notch filter to reduce power line interference [36].
FS1 is the Hudgins feature set [18]. FS2 is the feature set developed by Oskeoi and Hu [15]
that was observed to perform well for motion classification. FS3 is a feature set consisting of spike
shape features [14]. All features were calculated from the signal collected over the entire motion. One
feature was obtained for each muscle. For example, for FS1 there were 4 features times 7 sEMG muscle
channels for a total of 28 features in the feature vector for each segment. Feature values for healthy and
injured limbs from the same patient were calculated independently. The features were not adjusted so
that direct comparisons could be made between the healthy and injured limbs of individual patients.
3.4. Classification
Classification models were developed and evaluated for each of the ten motions separately. The
LDA, SVM, and RF classification models were investigated. The LDA classifier was selected because it
is simple, and has been found to be effective for classifying EMG signals in the literature. The SVM
classifier was selected as an extension of the LDA classifier. The RF classifier was selected due to its
usefulness for classifying stroke rehabilitation outcomes [28]. The RF classifier was generated from
200 decision trees. Classification models were initially developed to distinguish between healthy and
injured limbs. The classification models were also investigated for distinguishing between patients at
two different stages of rehabilitation: 0–6 weeks and 7+ weeks.
3.5. Evaluation
The classification accuracies for the feature sets extracted from each motion were evaluated for the
LDA, SVM, and RF models. The classification accuracies were computed using a leave-one-patient-out
cross-validation method. One patient was used as a test set, and the remaining patients were used
as the training set. This process was repeated for each patient. The accuracy was calculated as the
number of correct classifications divided by the total number of patients.
distinguishable. The computational complexity of a feature set should be kept as low as possible to
reduce the feature extraction time and the hardware memory requirements [37].
The RELIEFF feature selection algorithm [38] provides a weight for each feature based on its
predictive ability. The algorithm iterates through instances of each feature and searches for the k-nearest
neighbours in the same class (nearest hits) and from a different class (nearest misses). A good feature
has a similar value to the nearest hit classes, and a very different value from the nearest miss classes.
The differences between each feature instance and the nearest hits are added to the feature weight, and
the differences between each feature instance and the nearest misses are subtracted from the feature
weight. Feature weights are scaled on the interval [−1,1]. The best individual features were found by
comparing their individual performance in a majority vote model. The RELIEFF algorithm [38] was
used with the number of k-nearest neighbours to search for set to 10, as recommended in [28] to search
for the best combinations of features within a feature set.
Following the development and testing of the various classification models, the influence of
patient characteristics (sex, age, body mass index (BMI), and the time since injury) on the outcomes
of the models was investigated. Age was divided into three categories: (1) <30 (n = 8), (2) 30–45
(n = 13), (3) >45 (n = 6). BMI was divided into categories of normal (18.5–25), overweight (25–30),
and obese (>30). Each BMI category contained nine patients. Three categories of time since injury
were investigated: healthy, the early stages of rehabilitation (0–6 weeks of therapy), and the late stages
of rehabilitation (7+ weeks of therapy). The rationale behind these divisions was that strengthening
rehabilitation exercises begin at 7–8 weeks of therapy [4,5]. As well, patients in later stages of
recovery have been observed to have more similar EMG metrics to healthy subjects [25]. The patient
characteristics were input into the classification models as non-zero ordinal categories, and the models
were reevaluated.
4. Results
Table 2. Classification accuracies for each preliminary feature set. The best classification result for each
motion within each feature set is in bold.
Classification
Feature Set Motions
Accuracy (%)
LDA SVM RF
EF 62.3 60.5 70.3
EE 65.4 62.3 71.6
P 69.1 67.9 67.3
S 60.5 62.3 68.5
FS1
WF 67.3 56.8 69.1
(MAV, SSC,
WE 55.6 64.8 56.8
WL, ZC)
UD 58.6 62.3 71.6
RD 61.7 65.4 66.0
HC 64.8 54.9 72.2
HO 55.6 61.1 57.4
EF 59.9 57.4 67.9
EE 61.7 64.8 69.8
P 67.3 49.4 71.6
S 58.6 54.9 69.8
FS2 WF 63.6 59.3 65.4
(RMS, AR2) WE 60.5 54.3 59.9
UD 62.3 57.4 63.0
RD 59.1 45.9 69.2
HC 63.0 56.2 66.7
HO 58.6 64.2 63.0
EF 74.1 61.1 64.8
EE 61.1 77.8 68.5
P 72.2 63.0 61.1
S 50.0 63.0 72.2
FS3
WF 79.6 64.8 75.9
(MSA, MSF, MSS,
WE 57.4 66.7 64.8
MNPPS, MSD)
UD 72.2 68.5 61.1
RD 61.1 77.8 57.4
HC 57.4 59.3 64.8
HO 48.2 50.0 51.9
Table 4. Majority vote classification accuracies for individual features. Features are ordered by LDA
classification accuracy. The best classifier result for each feature is in bold.
Classification Classification
Feature Feature
Accuracy (%) Accuracy (%)
LDA SVM RF LDA SVM RF
MFL 76.54 73.45 59.88 MMAV1 64.81 54.94 62.35
MYOP 74.69 66.67 58.64 HFD 64.20 62.35 59.88
MSD 74.69 54.94 55.56 MAVS 64.20 50.00 56.17
AR4 74.07 59.88 50.00 PKF 63.58 67.9 61.11
MSF 72.84 72.84 54.94 MAV 63.58 55.60 64.81
MNPPS 70.99 64.20 52.47 MSA 63.58 53.70 62.35
PSR 70.99 66.67 56.17 MTW 62.96 50.62 64.20
ApEn 69.14 65.43 57.41 RMS 62.35 57.41 65.43
LOG 69.14 57.41 63.58 MHW 61.73 51.85 62.34
MNF 69.14 68.52 54.32 SM3 60.49 61.73 60.49
ZC 68.52 62.35 55.56 MNP 59.88 52.47 63.58
DASDV 68.52 51.85 61.73 TTP 58.79 51.85 64.20
VCF 68.52 57.41 56.17 VAR 58.64 52.47 64.20
AAC 67.90 51.85 59.88 FR 58.02 67.90 58.02
MSS 67.90 51.85 56.17 SM1 58.02 51.85 61.11
MMAV2 67.38 54.32 61.73 SKEW 57.41 53.09 50.00
WL 66.05 51.85 56.17 DFA 56.80 46.30 50.00
CC4 66.05 51.23 50.62 SM2 55.56 56.79 59.23
MDF 65.43 65.43 56.79 WAMP 54.32 56.17 50.62
SampleEn 65.43 64.81 56.17 KURT 52.47 53.70 50.00
SSC 64.81 61.73 51.85
The individual feature models classified between healthy and injured limbs with accuracies
ranging from 46.3–76.5%. The LDA classifier provided the highest classification accuracy for 27/41
of the individual features, therefore the following features were ranked the highest for each feature
category: LOG (time domain: energy), DASDV (time domain: information complexity), MYOP (time
domain: frequency), MAVS (time domain: multi-window), PSR (frequency domain), MSD (spike shape
analysis), AR4 (prediction model coefficients), ApEn (entropy), MFL (fractal dimension), and SKEW
(higher order statistics).
Table 5. Classification accuracies for each feature set. The best classification result for each motion
within each feature set is in bold.
Classification
Feature Set Motions
Accuracy (%)
LDA SVM RF
EF 78.4 70.4 63.6
EE 68.5 65.4 67.3
P 71.6 70.4 63.6
S 72.2 71.0 70.4
FS4 WF 70.3 70.4 70.4
(MFL, MYOP) WE 66.0 60.5 57.4
UD 77.2 79.6 67.3
RD 74.7 69.1 67.9
HC 69.8 69.8 63.6
HO 63.0 70.4 63.6
EF 61.7 73.5 71.0
EE 75.9 72.8 72.8
P 59.9 66.7 67.9
FS5 S 58.0 71.0 67.9
(LOG, DASDV, MYOP, WF 64.8 59.9 69.1
MAVS, PSR, AR4, WE 51.9 58.6 63.0
ApEn, MFL, MSD) UD 69.1 74.7 64.8
RD 61.1 73.5 67.3
HC 56.2 63.6 67.3
HO 56.8 64.8 60.5
EF 69.8 71.6 64.8
EE 72.5 72.2 75.9
P 72.8 70.4 66.0
S 71.0 72.8 70.4
FS5 Optimized
WF 56.8 69.1 68.5
with RELIEFF
WE 61.7 66.7 64.2
(PSR, MFL, MSD)
UD 72.2 76.5 69.1
RD 67.3 64.8 68.5
HC 65.4 71.0 61.7
HO 63.6 66.7 71.6
Table 6. Majority vote classification accuracies. Majority vote decisions were developed from all ten
motions, from only the top motions (EF, EE, P, S, WF, UD, and HC), and from a weighted majority vote.
The best classification results within each feature set are in bold.
Classification
Feature Set Motions
Accuracy (%)
LDA SVM RF
All 67.9 69.8 71.0
FS1
Top 70.4 69.1 75.3
Weighted 72.2 71.0 74.1
All 70.4 58.6 69.8
FS2
Top 69.1 60.5 67.9
Weighted 73.5 64.8 75.3
All 71.6 74.7 71.6
FS3
Top 72.2 72.8 74.1
Weighted 71.6 73.5 77.2
All 77.8 73.4 62.3
FS4
Top 79.6 77.8 64.2
Weighted 82.1 74.1 71.0
All 64.8 73.5 66.7
FS5
Top 68.5 76.5 65.4
Weighted 67.3 75.9 75.3
FS5 Optimized All 74.1 74.8 63.0
with RELIEFF Top 74.1 77.2 62.3
Weighted 79.6 81.5 77.2
A weighted majority vote decision was also applied to the individual motion models. Each model
was weighted by its respective classification accuracy. For example, when using the LDA classifier
with FS1, the weights for each decision model were selected as follows: EF = 62.3, EE = 65.4, etc.,
based on the classification results found in Table 2. The sum of the weights of the decision models that
identified the patient as healthy was determined, as well as the sum of the weights of the models that
identified the patient as injured. The highest sum (representing either healthy or injured) was selected
as the final weighted majority vote decision. The weighted majority vote classification accuracies
ranged from 64.8–77.2%, and the weighted vote provided improvements to the basic majority vote
classification accuracy for all models.
5. Discussion
The feature sets recommended in the literature were first explored for classifying muscle health.
When compared to FS1, FS2 performed similarly with the various classifiers, but had an overall worse
performance than FS1. FS3 was unique in that there was not a single classifier that was the best;
however, FS3 also provided the highest accuracies out of all feature sets. These observations are
consistent with the literature, which suggests that feature set selection is more important than classifier
selection for obtaining high classification accuracy with EMG signals [36].
The addition of more features in the feature set can improve accuracy, until an asymptote is
reached, at which point adding new features will not improve the accuracy [13]. The inclusion of four
features in FS1 compared to two in FS2 could account for the better classification performance of FS1.
Sensors 2019, 19, 3309 13 of 15
Likewise, FS3 contained the greatest number of features of the three feature sets tested, and displayed
higher accuracies than FS1 and FS2.
The LDA classifier tended to provide better classification for individual features; however, the RF
classifier provided better accuracies when used with feature sets. As the RF classifier can classify based
on nonlinear relationships between features, this may have contributed to the higher performance
when used with feature sets.
The EE motion was found to provide best classification, and the WE, HO, and RD motions were
found to provide poor classification accuracies. The WE, HO, and RD motions are hand and wrist
motions, therefore, the performance of these motions may be less impacted by an injury to the elbow.
For example, the HO motion involves the relaxation of the forearm muscles as the hand is released from
the closed position, which may be less strenuous on the elbow. The lower classification performance
may also be due to the muscles involved in the motion. The primary muscles involved in RD, the
extensor carpi radialis and the flexor carpi radialis, were not used as inputs for the classification
models. The WE motion is primarily performed by the ECU muscle, which suggests that the activation
of the ECU muscle is less informative for assessing elbow muscle health.
The RELIEFF algorithm identified the MFL, MYOP, PSR, and MSD features as preferable for
identifying muscle health. The feature set FS4 provided the highest classification accuracy achieved
(82.1%). Although not ideal, this sets a baseline for future comparisons.
This study used the injured and uninjured limbs of the same participants. This design ensured
that the healthy and injured data sets were matched for the population of patients (in terms of age, sex,
and BMI) presenting at clinics with elbow trauma injuries. However, this design does not consider
potential differences in muscle activity due to handedness. For example, research suggests that biceps
activity is lower in the dominant arm [39]. Overuse of the healthy limb to compensate for the loss of
function in the injured limb could also have influenced the results.
ROM and strength recovery were not measured in this study. It is recommended that for future
studies, a cohort of patients should be observed at multiple stages over the recovery process, to observe
healing patterns within individuals.
The purpose of the model was to allow for an objective metric of muscle health to be determined
that could identify if a patient was healing. This work was also directed towards identifying trends in
EMG behaviour that reflect muscle health following elbow trauma. EMG has been used to study the
muscle health of patients with neuromuscular injuries; however, no models have yet been developed
to identify and diagnose the muscle health of elbow trauma patients. This is the first model of its
kind. There is evidence that this could be a precursor to developing a more advanced model of muscle
health, so that a patient could be monitored as they progress through the rehabilitation process.
To develop a practical model of muscle health for a wearable device with multiple classes of
patient health, future work should be directed towards collecting data from a larger cohort of patients
with similar injuries, or from the same patients at multiple stages of recovery.
6. Conclusions
This paper introduced and evaluated a method of using sEMG signals to classify subjects between
two levels of upper-limb muscle health. The models developed achieved classification accuracies
of 45.9–82.1%. The healthy and injured data sets were collected from the same patient, so that the
healthy data sets can be compared to the injured sets, and can allow for a better representation of the
population of patients (in terms of age, sex, BMI) presenting at clinics with elbow trauma injuries.
EMG features capable of predicting muscle health were identified. The best individual features were
identified to be MFL, MYOP, PSR, and spike shape analysis features, in particular MSD. The best
individual motions for classifying health were EF, EE, P, S, WF, UD, and HC. The first classification
models to distinguish between healthy and injured limbs of elbow trauma patients based on EMG
data were developed. There is the potential for implementing a classification model of health in a
rehabilitative elbow brace to assess patients recovering from elbow trauma; however, further work in
Sensors 2019, 19, 3309 14 of 15
this direction, including further data collection, validation, optimization, and improvements to the
existing state-of-the-art EMG acquisition systems will be necessary to achieve this goal.
Author Contributions: Data collection, E.F.; conceptualization and supervision, A.L.T.; recruitment, patient
recruitment, S.C.; data analysis and validation E.F. and D.J.L.; the main content of this manuscript was created
and written by E.F. and reviewed by all authors.
Funding: This work was funded by the Natural Sciences and Engineering Research Council (NSERC) of Canada
under grant RGPIN-2014-03815 and by the Ontario Ministry of Economic Development, Trade and Employment
and the Ontario Ministry of Research and Innovation through the Early Researcher Award (A. L. Trejos). Financial
support for E. Farago was provided by a Transdisciplinary Bone & Joint Training Award from the Collaborative
Training Program in Musculoskeletal Health Research (CMHR) at Western University, and by an NSERC Canada
Graduate Scholarship.
Conflicts of Interest: The authors declare no conflict of interest.
References
1. Canadian Institute of Musculoskeletal Health and Arthritis. IMHA Strategic Plan 2014–2018. 2014. Available
online: http://www.cihr-irsc.gc.ca/e/48830.html/ (accessed on 28 May 2019).
2. Maciejasz, P.; Eschweiler, J.; Gerlach-Hahn, K.; Jansen-Troy, A.; Leonhardt, S. A survey on robotic devices for
upper limb rehabilitation. J. Neuroeng. Rehabil. 2014, 11, 3. [CrossRef] [PubMed]
3. Myomo. 2018. Available online: http://myomo.com/ (accessed on 28 May 2019).
4. Chinchalkar, S.J.; Szerkeres, M. Rehabilitation of elbow trauma. Hand Clin. 2004, 20, 363–374. [CrossRef]
[PubMed]
5. Fusaro, I.; Orsini, S.; Stignani Kantar, S.; Sforza, T.; Benedetti, M.G.; Bettelli, G.; Rotini, R. Elbow rehabilitation
in traumatic pathology. Musculoskelet. Surg. 2014, 98, S95–S102. [CrossRef] [PubMed]
6. Macdermid, J.C.; Vincent, J.I.; Kieffer, L.; Kieffer, A.; Demaiter, J.; Macintosh, S. A survey of practice patterns
for rehabilitation post elbow fracture. Open Orthop. J. 2012, 6, 429–439. [CrossRef] [PubMed]
7. Yousefi, J.; Hamilton-Wright, A. Characterizing EMG data using machine-learning tools. Comput. Biol. Med.
2014, 51, 1–13. [CrossRef]
8. Adel, T.; Smith, B.; Urner, R.; Stashuk, D.; Lizotte, D.J. Generative multiple-instance learning models
for quantitative electromyography. In Proceedings of the 29th conference on Uncertainty in Artificial
Intelligence (UAI), Corvallis, OR, USA, 11–15 August 2013.
9. Page, C.; Backus, S.I.; Lenhoff, M.W. Electromyographic activity in stiff and normal elbows during elbow
flexion and extension. J. Hand Ther. 2003, 16, 5–11. [CrossRef]
10. Nazmi, N.; Rahman, M.A.A.; Yamamoto, S.I.; Ahmad, S.A.; Zamzuri, H.; Mazlan, S.A. A review of
classification techniques of EMG signals during isotonic and isometric contractions. Sensors 2016, 16, 1304.
[CrossRef]
11. Chowdhury, R.H.; Reaz, M.B.I.; Ali, M.A.B.M.; Bakar, A.A.A.; Chellappan, K.; Chang, T.G. Surface
electromyography signal processing and classification techniques. Sensors 2013, 13, 12431–12466. [CrossRef]
12. Phinyomark, A.; Quaine, F.; Charbonnier, S.; Serviere, C.; Tarpin-Bernard, F.; Laurillau, Y. EMG feature
evaluation for improving myoelectric pattern recognition robustness. Expert Syst. Appl. 2013, 40, 4832–4840.
[CrossRef]
13. Phinyomark, A.; Phukpattaranont, P.; Limsakul, C. Feature reduction and selection for EMG signal
classification. Expert Syst. Appl. 2012, 39, 7420–7431. [CrossRef]
14. Gabriel, D.A.; Lester, S.M.; Lenhardt, S.A.; Cambridge, E.D.J. Analysis of surface EMG spike shape across
different levels of isometric force. J. Neurosci. Methods 2007, 159, 146–152. [CrossRef] [PubMed]
15. Oskoei, M.A.; Hu, H. Support vector machine-based classification scheme for myoelectric control applied to
upper limb. IEEE Trans. Biomed. Eng. 2008, 55, 1956–1965. [CrossRef] [PubMed]
16. Pincus, S.M. Approximate entropy as a measure of system complexity. Proc. Natl. Acad. Sci. USA 1991,
88, 2297–2301. [CrossRef] [PubMed]
17. Phinyomark, A.; Phukpattaranont, P.; Limsakul, C. Fractal analysis features for weak and single-channel
upper-limb EMG signals. Expert Syst. Appl. 2012, 39, 11156–11163. [CrossRef]
18. Hudgins, B.; Parker, P.; Scott, R.N. A new strategy for multifunction myoelectric control. IEEE Trans.
Biomed. Eng. 1993, 40, 82–94. [CrossRef] [PubMed]
Sensors 2019, 19, 3309 15 of 15
19. Richman, J.S.; Moorman, J.R. Physiological time-series analysis using approximate entropy and sample
entropy. Am. J. Physiol. Heart Circ. Physiol. 2000, 278, H2039–H2049. [CrossRef] [PubMed]
20. Englehart, K.; Hudgins, B. A robust, real-time control scheme for multifunction myoelectric control. IEEE
Trans. Biomed. Eng. 2003, 50, 848–854. [CrossRef] [PubMed]
21. Calder, K.M.; Gabriel, D.A.; McLean, L. Differences in EMG spike shape between individuals with and
without non-specific arm pain. J. Neurosci. Methods 2009, 178, 148–156. [CrossRef]
22. Zhao, J.; Jiang, L.; Cai, H.; Liu, H.; Hirzinger, G. A novel EMG motion pattern classifier based on wavelet
transform and nonlinearity analysis method. In Proceedings of the IEEE International Conference on
Robotics and Biomimetics, Kumming, China, 17–20 December 2006; pp. 1494–1499.
23. Nazarpour, K.; Al-Timemy, A.H.; Bugmann, G.; Jackson, A. A note on the probability distribution function
of the surface electromyogram signal. Brain Res. Bull. 2013, 90, 88–91. [CrossRef]
24. Hogrel, J.Y. Clinical applications of surface electromyography in neuromuscular disorders. Neurophysiol. Clin.
2005, 35, 59–71. [CrossRef]
25. Haddara, R.; Zhou, Y.; Chinchalkar, S.; Trejos, A.L. Postoperative healing patterns in elbow using
electromyography: Towards the development of a wearable mechatronic elbow brace. In Proceedings of the
IEEE International Conference on Rehabilitation Robotics, London, UK, 17–20 July 2017; pp. 1395–1400.
26. Fougner, A.; Scheme, E.; Chan, A.D.; Englehart, K.; Stavdahl, Ø. Resolving the limb position effect in
myoelectric pattern recognition. IEEE Trans. Neural Syst. Rehabil. Eng. 2011, 19, 644–651. [CrossRef]
[PubMed]
27. Subasi, A. Classification of EMG signals using PSO optimized SVM for diagnosis of neuromuscular disorders.
Comput. Biol. Med. 2013, 43, 576–586. [CrossRef] [PubMed]
28. Patel, S.; Hughes, R.; Hester, T.; Stein, J.; Akay, M.; Dy, J.; Bonato, P. Tracking motor recovery in stroke
survivors undergoing rehabilitation using wearable technology. In Proceedings of the IEEE Engineering
in Medicine and Biology Society Conference, Buenos Aires, Argentina, 31 August–4 September 2010;
pp. 6858–6861.
29. Toledo-Pérez, D.C.; Martínez-Prado, M.A.; Gómez-Loenzo, R.A.; Paredes-García, W.J.; Rodríguez-Reséndiz, J.
A Study of Movement Classification of the Lower Limb Based on up to 4-EMG Channels. Electronics 2019,
8, 259. [CrossRef]
30. Scheme, E.; Englehart, K. Electromyogram pattern recognition for control of powered upper-limb prostheses:
State of the art and challenges for clinical use. J. Rehabil. Res. Dev. 2011, 48, 643–660. [CrossRef] [PubMed]
31. Subasi, A.; Kiymik, M.K. Muscle fatigue detection in EMG using time-frequency methods, ICA and neural
networks. J. Med. Syst. 2010, 34, 777–785. [CrossRef]
32. De la Peña, S.; Polo, A.; Robles-Algarín, C. Implementation of a Portable Electromyographic Prototype for
the Detection of Muscle Fatigue. Electronics 2019, 8, 619. [CrossRef]
33. SENIAM project. Sensor placements. Available online: http://seniam.org/ (accessed on 28 May 2019).
34. Drapała, J.; Brzostowski, K.; Szpala, A.; Rutkowska-Kucharska, A. Two stage EMG onset detection method.
Arch. Control Sci. 2012, 22, 427–440. [CrossRef]
35. Solnik, S.; Rider, P.; Steinweg, K.; Devita, P.; Hortobágyi, T. Teager-Kaiser energy operator signal conditioning
improves EMG onset detection. Eur. J. Appl. Physiol. 2010, 110, 489–498. [CrossRef]
36. Hakonen, M.; Piitulainen, H.; Visala, A. Current state of digital signal processing in myoelectric interfaces
and related applications. Biomed. Signal Process. Control 2015, 18, 334–359. [CrossRef]
37. Zardoshti-Kermani, M.; Wheeler, B.C.; Badie, K.; Hashemi, R.M. Feature evaluation for movement control of
upper extremity prostheses. IEEE Trans. Rehabil. Eng. 1995, 3, 324–333. [CrossRef]
38. Kononenko, I.; Šimec, E.; Robnik-Šikonja, M. Overcoming the myopia of inductive learning algorithms with
RELIEFF. Appl. Intell. 1997, 7, 39–55. [CrossRef]
39. Bagesteiro, L.B.; Sainburg, R.L. Handedness: Dominant Arm Advantages in Control of Limb Dynamics.
J. Neurophysiol. 2002, 88, 2408–2421. [CrossRef] [PubMed]
c 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY) license (http://creativecommons.org/licenses/by/4.0/).