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Review

Wearable Solutions for Patients with Parkinson’s Disease and Neurocognitive Disorder: A Systematic Review

Computer Science Department, University POLITEHNICA of Bucharest, RO-060042 Bucharest, Romania
*
Author to whom correspondence should be addressed.
Sensors 2020, 20(9), 2713; https://doi.org/10.3390/s20092713
Submission received: 9 April 2020 / Revised: 5 May 2020 / Accepted: 6 May 2020 / Published: 9 May 2020
(This article belongs to the Special Issue State-of-the-Art Sensors Technology in Romania 2020)

Abstract

:
Prevalence of neurocognitive diseases in adult patients demands the use of wearable devices to transform the future of mental health. Recent development in wearable technology proclaimed its use in diagnosis, rehabilitation, assessment, and monitoring. This systematic review presents the state of the art of wearables used by Parkinson’s disease (PD) patients or the patients who are going through a neurocognitive disorder. This article is based on PRISMA guidelines, and the literature is searched between January 2009 to January 2020 analyzing four databases: PubMed, IEEE Xplorer, Elsevier, and ISI Web of Science. For further validity of articles, a new PEDro-inspired technique is implemented. In PEDro, five statistical indicators were set to classify relevant articles and later the citations were also considered to make strong assessment of relevant articles. This led to 46 articles that met inclusion criteria. Based on them, this systematic review examines different types of wearable devices, essential in improving early diagnose and monitoring, emphasizing their role in improving the quality of life, differentiating the various fitness and gait wearable-based exercises and their impact on the regression of disease and on the motor diagnosis tests and finally addressing the available wearable insoles and their role in rehabilitation. The research findings proved that sensor based wearable devices, and specially instrumented insoles, help not only in monitoring and diagnosis but also in tracking numerous exercises and their positive impact towards the improvement of quality of life among different Parkinson and neurocognitive patients.

1. Introduction

Nowadays, millions of people are bearing cognitive deterioration [1]. There is an extensive range of neurocognitive disorders specified as Alzheimer’s disease, Parkinson’s disease, Traumatic brain injury, Lewy body disease, Vascular disease, Frontotemporal lobar degeneration, etc. [2,3]. Comparatively, Parkinson’s disease (PD) is the second most frequently observed neurodegenerative disease [4]. Around seven to ten million people in the world have Parkinson’s disease. The examination of Parkinson’s disease is a tricky one; research has been done for decades and still there is no robust test that serves as the best since Parkinson’s disease signs and symptoms vary from person to person and its features are very similar to other illnesses [5]. PD can be investigated incorrectly and can be interpreted with other diseases. Characterization of tremors in hands and gait features plays a vital role in diagnosis and long-term monitoring of Parkinson patients.
Typical gait disorders of PD can be illustrated as freezing of gait (FOG), stooped posture, shuffling steps, festination, and falling [6]. Current clinical solutions for detecting gait use motion sensing technology i.e., camera-based optical motion-capture system, markers attached with body, force plated on the ground to measure pressure, equipped treadmills with different sensors and for quantifying tremors, laser displacement sensors, and electromyography (EMG) systems [7,8] are used. For diagnosis, assessment, and monitoring, there is a need for continuous data from patients and the solution lies in wearable technology [9]. The role of wearables is multifold, and it starts from continuously capturing the motion data [10] that helps in diagnosis, monitoring, and tracking the changes in compliance with exercise training, boosting, and also from clinical trial data. It does not only monitor PD symptoms but helps in improving them. Hence, the aim of this systematic review is to find the use of sensor based wearable devices in the diagnosing and monitoring of PD patients, analyzing their role in enhancing PD patients’ quality of life (QoL) and clearly identifying how wearables can help in finding the results of various fitness and rehabilitation exercises.

2. Method

2.1. Data Collection

Our systematic literature review collected publications from January 2009 to January 2020 from the following databases: Elsevier, IEEE Xplorer, and PubMed/Medline. Our search for finding relevant articles is comprised of five stages based on Preferred Reporting Items for Systematic Reviews and Meta Analyses (PRISMA) as shown in Figure 1 and Figure 2. In the initial stage, we used three combinations of keywords: “wearable sensors AND Parkinson disorder”, “wearable sensors AND neurocognitive disorder”, “Parkinson patients AND rehabilitation exercises” in the three databases mentioned above, and we got around 3158 articles as result. We also added 102 relevant articles found from other sources with these keywords and hence we got 3260 articles as shown in Table 1.
In the second stage, we initially removed 271 duplicates since the same articles were found in different databases, and we also removed articles on the basis of careful analysis of titles and abstracts. In this way, 740 records were obtained as shown in Table 2. In the third stage, we filtered out the articles and considered the ones which are ISI indexed. Based on this criteria, we got 639 articles as shown in Table 3.
In the fourth stage, we have developed our own customized PEDro inspired scoring that classified the most relevant articles fitted for our system review. In PEDro, five statistical indicators are set as answers to the following questions:
  • Does this article prove that wearable sensors can be used to quantify recovery automatically in a laboratory setting?
  • In this article, were wearable sensors used to monitor people remotely in their home?
  • How many patients/subjects participated in this study?
  • Does this article discuss the exercise rehabilitation that can enhance the recovery and fitness in (PD) patients?
  • Is this a Survey/Review article?
In this way, the articles were analyzed by means of the answers to these above presented questions and we selected those publications that obtained at least four points (“fair”/“high” quality), by applying the following grading criteria as represented in Equations (1) and (2):
Q n * = r = 1 n = 5 Q r
Q n * = Q n * Q n * < 4 4 Q n * 4
Q3 refers to the number of human subjects included in the study for each article, and it is shown in Table 4. However, this standard does not apply for review articles—for survey papers, a different perspective is set, following the same calculations. In this case, the references’ quality was considered as depicted in Table 5. For each criterion, the maximum number of points possible to be obtained was 1.
A balance between the newly published articles with less number of citations and the older ones which have more citations have been considered further. For this reason, a new tailored formula is developed. Its purpose is counting the number of citations obtained each year for each article starting from the year in which the article was published. Some steps should be mentioned at this point. In the first stage, Equation (3) gives the number of citations registered every year for one candidate article:
P Y C i = T C i 2020 Y i
In the above equation, PYC represents the number of citations per year, TC shows the total number of citations, and Y specifies the year when the article was published. The equation takes into account the idea that some articles are published in different years and the number of citations depends on this aspect. Thus, the newer articles have a different weight than the older ones. In this context, Equation (4) presents the method of computing the absolute value of quality Qi* for an article from the citation point of view:
Q i * = 5 P Y C i m a x j = 1 n ( P Y C j ) + 6 m i n ( 2020 Y i , 6 ) 2
As it will be seen in Equation (5), all of the absolute values should be inside the interval [0:5]. This final value Qi has been chosen to range the maximal score up to 10 because the total score of each article is, in fact, the average of each statistical indicator multiplied by 2:
Q i = { Q i * , Q i * < 5 5 , Q i * 5
All these selection criteria have been applied according to the discussed equations and the final number of articles remained to be analyzed became 46. The systematic review will focus further on the analysis of this reduced set.

2.2. Method of Analysis

After we created our collection of the most relevant articles by the quantitative analysis, the next phase regards the qualitative analysis of the remaining 46 articles. Considering the main purpose of this systematic review, we further investigated them following some relevant research questions as:
  • Does motor disability play any role in altering the quality of life of PD patients?
  • Do wearable insoles help in diagnosis, monitoring, and rehabilitation of PD patients?
  • Which gait or fitness exercise impact the quality of life?
  • Which fitness tests lead in proper diagnosis of balance, walking, and aerobics fitness of PD patients?

3. Outcomes of the Systematic Review

This section is divided into four parts. Each of them revolves around the main aims of this systematic review.

3.1. Early Diagnosis Wearables and the Effects of Motor Disorders on Quality of Life (QoL)

Preponderance of Parkinson’s and overall motor symptoms affects the QoL of PD patients very badly [11]. Gait disorders are classified according to an accepted scheme and their associations to falls. Neuro-psychological measures and QoL have been explored for decades, a fact that proved that gait impairments significantly diminish QoL. The main motor disabilities faced by PD patients are elaborated in Table 6 and Figure 3. Gait disorders are the most common among PD patients, reducing the mobility in the daily life activities and becoming worse as disease advances [12]. The difference between normal and Parkinsonism gait can be seen in Figure 3. Hence, PD leads to major walking problems, causing falls and hence leading to long-term disability and independence loss.
The role of wearables in improving early diagnosis and monitoring is further analyzed considering the great improvements brought by the wearable devices proposed by so many researchers in this field. The most promising role can be played by the wearables which are less expensive, consume less power, are unobtrusive, and provide more accurate data in diagnosing, monitoring, and managing a rehabilitation process. Wearables in PD applications may be helpful in early diagnosis, tremor, body motor fluctuations, and home and long-term assessment as discussed in [13]. Currently, PD diagnosis relies on monitoring the motor and non-motor significance and usually doctors check the severity of PD patients disease by asking them to perform specific tasks and assign them scores based on Unified Parkinson Disease Rating Scale (UPDRS) or Movement Disorder Society-sponsored revision of UPDRS and Hoehn and Yahr scale. Many times, the result provides a 40% wrong diagnosis because of the inter-rater variability among different examiners. Early, prompt, and accurate diagnosis of PD may improve QoL and, regarding this, wearables play a fundamental role in helping clinicians perform early diagnosis and objective quantification. In [14], the researchers proposed a pedestrian dead reckoning (PDR)-based method using a smartphone. The accelerometer sensor in a smartphone monitors the changes of walking patterns of subject like PD and captures the gait characteristics, such as step length and step frequency. This early warning diagnosing tool gives about 98% accuracy of step length estimation. In [15], researchers introduced another early diagnosing wearable wireless system with a proprietary algorithm. The system is composed of IMUs attached on the patient’s lower limb. The system is tested on 20 subjects and showed promising results, the maximum error in stride number estimation was as low as three units.
Tremor is the most frequently observed symptom among PD patients. It appears in 70% of them. In [16], a custom-developed device (SNUMAP) is designed using an accelerometer and gyroscope, fabricated on a wrist module. The system is validated on 92 PD patients and showed more precise monitoring of PD tremors. In [17], a smartwatch is developed for PD tremor analysis which turns out to be very reliable, well-correlated with clinical scores, and well-accepted by patients for clinical follow-up. Bradykinesia is another symptom that severely affects QoL. In [18], the wearable IMUs are implemented to quantify whole body movements, producing Bradykinesia indices for walking (WBI) and standing up from a chair (sit-to-stand; SBI) and compute an objective score for whole body Bradykinesia.
The concept of monitoring patients in their own homes is the future trend in long-term monitoring. In this context, [19] proposed a multi-sensor monitoring unit (WMSMU) called PERFORM for monitoring, assessment, and management of patients. In [20], another system using IMUs and smartphone-based application served as an adequate gait training application in home infrastructure by improving postural balance and gait activity. The system gave auditory cueing to prevent or overcome FOG episodes. Similarly, the articles [21,22] proposed on-shoes wearable sensors and monitoring insoles that helps in gait assessment and monitoring. Thus, an optimal solution for improving monitoring and assisting PD patients lies in wearable technology which has been proven to be more flexible to be adopted in both clinical framework and in a home environment.

3.2. E-Health Wearables for PD Patients

The current demand of technology for PD appraisal, intervention, and rehabilitation varied in its requirements and can be counted from cost, usability, working, efficiency, design, and continuous quantitative and qualitative information [12]. In the beginning, clinical based scales were set to check motor symptoms severity which resulted in an uneven ratings and wrong measurements. The introduction of a smart environment such as body attached sensors, ubiquitous networking, and embedded sensors facilitates healthcare allied assistants to automatically monitor PD patients in real world environments. For instance, the researchers in [23] monitored full body tremor, which is one of the dominant symptoms among PD patients, using an inertial measurement unit (IMU) based motion capture system and detecting tremor against non-tremor dominant individuals among a group of 40 PD as well as from 20 healthy controls. In [24], the authors focused on another PD debilitating symptom that is freezing and discussed the variety of lightweight and wearable inertial sensors that may help in monitoring FOG (freezing of gate) in PD patients which uses dopaminergic medication. Similarly, in [25], the authors proposed a method for finding gait freezing events amid normal walking using skin conductance (SC) features and multivariate Gaussians.
The research study in [26] brings the key challenges in using wearable sensors i.e., data management, scalability, interoperability, standardization, security, and privacy and also proposed a smart glove in which flex sensors are attached to detect motor symptoms such as tremor, rigidity, and slowness of movement. The different endowed e-health wearables that assimilate contextual data are: DynaPort MiniMod Hybrid (worn on the lower back), Parkinson’s Kinetigraph (a wrist worn logger), a KinetiSense motion system (for dyskinesia measurements), ActivPAL, Stepwatch 3 (step activity monitor), Shimmer (records walking and turning), Mobi8Senior mobility monitor (SMM, Philips), SENSE-PARK system (for gait, hypokinesia, dyskinesia, sleeping), GAITrite (gait analysis systems), Opal (to asses quality of turning), Actigraphs (to monitor sleep), and also cueing devices such as auditory cueing devices, visual cueing devices, and somatosensory stimuli devices [27,28,29,30,31,32,33]. All of these devices help in feature classifying of PDs determining the disease severity, motor impairment, and also the improvements after the exercises.

3.2.1. Wearable Device(s)

Most of the wearable devices are developed based on inertial sensors that are comprised of an accelerometer and gyroscope. Accelerometers are used to measure accelerations but are unable to measure the rotations or angles. Therefore, these can not help with detecting the turns during walking activities. On the other side, gyroscopes serve in detection of angular velocity of body and also there are less chances of mechanical noise than in an accelerometer’s case, hence turning is better assessed during motion. Being critical with gyroscopes, it can be mentioned that their drawback relates to the high power consumption during long-term recording. Battery life, type, and number of inertial sensors, sampling rate, recording and processing time, and, most importantly, the learning algorithm is the key factor that makes the difference between the accuracy and precision of wearable devices. In this section, we highlight the ones that assess motor symptoms of PD patients and offer insights in diagnosis, cueing, and testing.
In [27], the authors proposed a device named Opal, with a weight of 22 g. It is built using inertial sensors, a battery, and includes 8 GB of memory storage. The device is tested in a research study in which users wore three Opals, one on the belt and the remaining two inside shoes. Data were recorded at 128 Hz and later uploaded to a laptop. The data from this device help in assessing the quality of turning. The researchers in [29] introduced a Kinesia system that consists of a software application, a hybrid sensor worn on the finger, and an automated web-based symptoms assessment system. The patients wore the sensors on the index finger of the most affected hand. The assessment is based on five motor tasks each of 15 s to predict finger tapping, dyskinesia, hand opening and closing, and also the postural tremor. The Parkinson’s Kinetigraph from [30,32] is used to measure the wrist movements and is worn like a wrist bracelet. It weighs around 35 g, and it has a three-axis iMEMS accelerometer (ADXL345 analog device) that records acceleration with a value of ± 4 g at sampling frequency of 50 samples/s. The device is developed using a digital microcontroller with flash memory along with a rechargeable battery. The sensor apprehends the Bradykinesia and dyskinesia values in a two-minute span for 10 days using a fuzzy logic algorithm. The device is preferred to be worn at the most affected limb of PD patients. The GAITRite in [30] is a walkway with a length of 4.6 m connected with Windows XP through the serial port. The thickness of passageway is 1/800 and has 16,128 sensors attached between two layers of vinyl and a rubber. It helps with demonstrating Bradykinesia and can be used in the replacement of conducting a traditional timed test such as a TUG test or filling questionnaires from PD patients [28].
Actigraphs are movement detectors, which are constructed with accelerometers and a memory for recording the movements for few weeks. The programs are developed to determine the levels of rest/movement, rhythmic parameters, and running/sitting parameters. In [27], Actigraphs, in the form of wrist worn activity sensor, are used for sleep monitoring. The KinetiSense motion system in [30] served for accurate measurements of tremors, Bradykinesia, and dyskinesia. It is built using accelerometers and gyroscopes that are attached on three areas of the body. This system is considered to be beneficial in developing new therapies. Stepwatch 3 is called an ankle acceleromater, fixed on the leg for counting stride rate. It is one of the devices with most valid and reliable results in monitoring ambulatory activity as discussed in [27,30]. ActivPAL™ in [31] is a small, lightweight activity monitor device that has a uni-axial accelerometer fixed on the upper thigh, at 10 Hz sampling frequency. The raw data in form of spreadsheet are exported for further analysis in MATLAB. The SENSE-PARK System in [31] has a set of inertial sensors (three are used during daytime and one in night phase) that helps in detecting movements of PD subjects i.e., FOG, dyskinesia, tremor, and sleep using an algorithm. The system also has a Wii balance board for collecting information such as body weight and sway.
In the study [31], SHIMMER sensors are introduced. These are kinematic sensors developed with gyroscope and an accelerometer that performs sampling at 102.4 Hz. These are attached in the form of elastic bands. The recorded data are transferred to computer wireless using Bluetooth. A total of 21 features are selected for reliability analysis from the recorded data. Another ambulatory assessing device is Mobi8 proposed in [31], which is a multichannel data logger with a dimension of 11.4 × 9.8 × 3.7 cm 3 , weighs up to 165 g, has a 3D sensor (Analog Devices ADXL330), and is worn on the lower back. It records anterior-posterior, vertical, and mediolateral, respectively. For finding daily life activities such as walking, the Senior Mobility Monitor (SMM) [31] was implemented. It is comprised of an accelerometer and barometer. The data are sampled at 50 Hz for the accelerometer and 25 Hz for the barometer. SMM is required to be worn at sternum height. The data are analyzed using a wavelet-based decision tree algorithm in MATLAB®, version 2013a. DynaPort MiniMod Hybrid in [32] weighs 74 g and has dimensions of 87 × 45 × 14 mm. It is attached on a belt on the back to show lower body movements in performing DLA. The device consists of accelerometer with a limitation of ± 2 g, a resolution of ± 1 mg, and a triaxial gyroscope. The readings are stored on an SD card at a frequency of 100 Hz and transferred in MATLAB Software for further analysis of gait features. The system aids in monitoring and classifying the quality and quantity of gait in PD faller and non-faller groups.
The study [33] provides a technological review on available wearable cueing devices, highlighting the current auditory, visual, and somatosensory cueing devices. The auditory cueing devices include Android applications based on Google Glass, GaitAssist (equipped with two inertial sensors and a smartphone with android application and wired headphones), FoG detection devices with wireless ear sets, Metronome Peterson bodyBeat and Metronome SDM300 SAMICK (Peterson Electro-Musical Products, Inc., Alsip, IL, USA), and devices with a movement sensor enabled with Bluetooth and wired headphones. These devices produce a typical and distinctive sounding tones (i.e., tap, tick, click, and beat) in beats/minute. In this way, it generates temporal information such as step interval, through the rhythmical beat. Some visual cueing devices are: Laser shoes, Smart Gait-Aid (Android app on binocular smart glasses), and Visual-auditory walker. These devices demonstrated that visual stimuli can diminish the FOG occurrence during walking. Parallel patterns aid in conveying spatial parameters’ information, such as step duration. Some somatography cueing devices are: CueStim (two channel electrical stimulator), Vibrating waistband, and a Vibrating system named VibroGait.

3.2.2. Insoles Models and Technical Features

According to primary research studies, there are two ways to evaluate motion activities of PD patients: subjective and objective. The subjective methods are based on questionnaires, UPDRS criteria, or Hoehn and Yahr scales in which there are more chances of getting an incorrect evaluation and error in scaling. The objective assessment is based on a huge variety of body worn sensors such as accelerometers, gyroscopes, magnetometers, force sensors, etc. that detect each fine movement and angles of a person performing (daily life activities) DLA, but the criterion validity of these wearable e-health devices vary from one to another. Not all the aforementioned devices in [27,28,29,30,31,32,33] are appropriate for daily routines in people with Parkinson’s disorder, and it is hard to find a single wearable device for diagnosis, monitoring, and rehabilitation of PD. A systematic review in [34] provided a potential solution for continuous and unobstructed appraisal of Parkinson’s patients that resides in smart insoles.
There is no doubt that humans wear shoes continuously, and the insoles are much cheaper than other wearable devices commercially available in the market. Table 7 presents an overview of the insole models discussed in papers [35,36,37,38,39]. These insoles can extract gait features and help in classification of PD stages and in daily monitoring for rehabilitation purposes. The results of the comparative study [34] emphasize that the data validity of smart insoles is 75% to 100% accurate, 75% to 100% precise, and the specificity lies between 73% to 100%. In this way, we can say that smart wearables [40] allow quantitative, objective, and reliable evaluation of motor activities.

3.2.3. Algorithms for Analysis of Gait Pattern

However, besides the acquisition of a robust data set from wearable insoles, another noteworthy aspect regards the algorithms that accurately learn from the data and also accurately predict [41]. Machine learning algorithms are currently considered as the pervasive part of the smart environment, but PD data are different in a more sophisticated way from the traditional clinical data as it is comprised of high-frequency continuous digital sensors readings of around tens of thousands per second.
ML algorithms such as random forest (RF), decision trees (DTs), logistic regression (LR), support vector machine (SVM), hidden Markov models (HMMs), naive Bayes, clustering algorithms, and neural networks (NNs) have been implemented successfully in medicine [32] and recently expanded to use them for sensor based PD motor assessment. A systematic study [42] revealed that ML algorithms depend on the data and on the features that are needed to be extracted as it is discussed in [43], where a TRIS (treatment response objective index) algorithm is discussed that examines clinical effectiveness with regard to dose response.
The outcome of studying these insoles models proved that smart insoles can identify either the subjects are sitting, standing, walking, or lying and can also differentiate between normal gait and Parkinsonism gait features. Last but not least, these can be useful to find the improvements in movement after exercises.

3.3. Clinical Effects of Rehabilitation Exercises on PD Patients

Research has proved that gait disorder creates disability and determines poor QoL because of the cardinal symptoms i.e., FOG (freezing of gate), tremors, and falls in people with PD. Systematic reviews and guidelines confirmed that the motor exercise is an effective method to rectify the gait and the overall physical functioning, improving QoL. Many fitness exercises like physiotherapy, center or home based workouts, treadmill training, visual or acoustic cueing and upper and lower body strength exercises have become an integral part of managing Parkinson’s disease. However, clinical trials have been unsuccessful in identifying which motion oriented gait exercise method can give the best results. In this systematic review, one of our objectives is to compare the results of different training activities [44,45,46,47,48,49,50,51,52] as elaborated in Table 8, and to assess the overall changes in movement related disorders and QoL.
“Exercise is medicine” [49] are the perfect words that fit for PD patients. Improvement in QoL appears to be the most general form of rehabilitation, even if it is resulted just based on home exercises, tailored center based training, robotic, or treadmill. Our study based on different reported research works reveals the fact that most of the training is conducted outside the home [53]. Home based exercise gives similar results to the instrumental based one, and it is applied to patients who are not in an advanced stage of PD. It is also observed that cognitive and psychological rehabilitation is just at the beginning, but it is an emerging area of research. The majority of interventions missed taking inter-professional approach planned without the consent of patients and conducted in a home environment. Considering all the interventions, it is observed that PD rehabilitation needs more concentration and research. Coordination between distinctive health care professionals and multidisciplinary support teams is needed to tackle the complexity of PD and more work is needed in this area [54]. Such multidisciplinary support must be tailored keeping the desires and objectives of each individual PD patient.

3.4. Fitness Test for Objective Evaluation of Rehabilitation

After selecting the type of exercise, the location, approach, and the intensity duration required to achieve motor benefits, the next relevant concern is how to find a robust evaluation test that correctly shows the results of rehabilitation. The assessment of motor activity in PD has been growing in recent years among research communities. Previous rehabilitation tests have varied with every individual, but researchers have considered the timed up and go (TUG) test as more efficient. In this test, individuals are asked to perform some tailored motor activities (i.e., sitting, in stood posture, turning, climbing) and the positive feedback proves the improvement of specific rehabilitation training. However, the TUG test gives promising results by just counting on the total time taken by patients to complete the task, and addresses some lower extremities’ dysfunctions. These two factors are not enough for evaluation of PD patients’ motor recovery. Hence, numerous tests have been proposed in recent years. Table 8 depicts the type of test for each research study used to predict the amount of benefits of each training.
In addition to TUG tests acquired using the wearable sensors, two other examination methods using wearable sensors are described in articles like [38,39]. In [38], the Ambulosono wearable works with an iOS GaitReminder App that produces auditory instructions while continuously recording step sizes via iOS gyro and accelerometers (after correcting the limb length, angular excursion, signal filtering, and drift). During the tests, the patients uniformly received a set of standardized auditory instructions, tailored by clinical guidelines, through wireless headphones, which contain verbal encouragement, specification of walking speed (e.g., comfortable or fast), and reminders of completed walking time. Step features collected via GaitReminder App show an average of <10% difference when it was tested against direct video measurements, and an analogous error rate was conjointly found once the App was used for treadmill walking or over-ground walking activities. A new generation of the Ambulosono sensor was designed, and it demonstrated a <5% error rate in gait measurement.
Another wearable based method is the combination of TUG and different subsystems. As TUG gives promising results in evaluation of lower extremity dysfunctions, the total time to finish the TUG does not give insight into turning and transitioning from standing to sitting actions. Hence, [39] highlighted the importance of segmenting the TUG into phases. In their study, they proposed that IMU data should be extracted from an iPad coupled with a custom built application. The Cleveland Clinic Mobility and Balance Application (CC-MB) could be used to segment the TUG into the subtasks. However, the study is in an infant stage and needs validation and more work to verify the results.
Table 8 clearly emphasizes the idea that currently the TUG test and the 6 or 10 min walking test are mostly considered for evaluation. However, a new paradigm is set to quantify the rehabilitation phase using IMU (inertial measurement unit) for the TUG test [45]. The research is still in an incipient phase, but it can provide crucial factors that helps in distinguishing the recovery rates. In the case of upper limb neuro-rehabilitation, the researchers pay more attention to automatic assessment systems as they are described in the systematic review [46]. They proposed a framework of automated assessment rehabilitation systems that will be more autonomous and objective.
Table 8 clearly emphasizes the idea that the TUG test and 6 or 10 min walking test are mostly considered for evaluation. However, a new paradigm is set to quantify the rehabilitation phase using IMU (inertial measurement unit) for TUG test [55]. The research is still in an incipient phase, but it can provide crucial factors that helps in distinguishing the recovery rates. In the case of upper limb neuro-rehabilitation, the researchers pay more attention to automatic assessment systems as it is described in the systematic review [56]. They proposed a framework of automated assessment rehabilitation systems that will be more autonomous and objective.

4. Conclusions

In the context of fast development of wearable technologies, more and more solutions for diagnosis, rehabilitation, assessment, and monitoring of patients with Parkinson’s disease have been discussed and presented in the scientific literature. This systematic review is comprised of two parts. The first one regards a quantitative analysis in which we collected more than 3000 articles from four databases, based on the PRISMA technique. We used a PEDro inspired method to reduce our set to 46 worthy articles. Furthermore, in the second part, a qualitative analysis has been realized based on recent solutions developed for PD diagnosis and rehabilitation. Considering all the factors and research works, we can conclude that motor disability of Parkinson’s patients significantly reduces the QoL as it is not diagnosed at initial stages and the clinical diagnoses are based on UPDRS scaling and other clinical systems scoring that proved to be limited by individual assessment and patients’ status. The existing wearable technology is playing a leading role in terms of treatment, diagnosis, and motor activity improvement of PD.
Researchers have proposed many different wearable solutions for monitoring and diagnosis of PD by putting more efforts in finding the most dominant features during gait activity such as heel off, step length, stride length, stride time, and plantar pressure. The most suitable wearable sensor devices for finding these features are wearable insoles, IMU based monitoring systems attached at lower limb, smart bands, EMG based devices, Actigraphs, GAITrite, ActivPals, and gait monitoring system using a smart-phone equipped with inertial sensors. Among all these, the insoles proved to be more dominant and useful, suggesting that these wearable solutions must be exposed to a larger population for validity. From the selected articles, it is demonstrated that repetitive intense motion activities proved to be effective for PD patients especially to those with severe motor disabilities. Great advantages are observed with treadmill and sensory motor training’s but still the results depend on the optimal location, amount of training under supervision, mode of delivery, intensity of exercise, and the type of training required to get the benefits.
With respect to rehabilitation evaluation, the TUG, 6MWKT, and 10MWKT tests are traditional gold standard examination tests for monitoring gait deflation, providing treatment analysis such as of physical therapy and various exercises. However, these tests are time consuming and task performance related, and the results are affected by many multiple variables like walking area, task complexity assigned to patient, physical exertion by participant, and incapability to finish the task as a result of fatigue. Among these, the TUG test has been used for decades, but currently new methods are being introduced from which the automatic assessment system brings remarkable results. These wearable devices help not only for rehabilitation exercises and motor improvement but also in analyzing the evolution or involution of this disease. However, there is a lot of research and development work left in this healthcare area especially on the accuracy, precision, reliability, and objective support from patients and healthcare systems for validation and adoption of these wearable solutions.
As a high number of initiatives in the previous research shows that most of the wearable devices use uni-modal sensor or bi-modal sensors, in the future, we will investigate the effectiveness of the multi-modal sensor approach for the assessment of PD. Our next directions will also focus on the role of invasive sensors. The aforementioned technology in which sensors reside inside the patient body has been proved to be very useful providing continuous information for monitoring and also diminishing PD effects like tremor or bradykinesia. Hence, we will investigate the articles regarding the impact of invasive sensors on PD patients, challenges in operation of minimally invasive sampling techniques, their application to larger community for telemedicine or telehealthcare, and their useful deployment in healthcare industry.

Author Contributions

The concept of article is proposed by N.P., and the data resources and validation have been contributed by A.C. and V.C. The formal analysis, investigation, and draft preparation are performed by A.C. The supervision and review of study are headed by N.P. The final writing was critically revised by N.P. and V.C. and finally approved by all the authors. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the European Union’s Horizon 2020 Research and Innovation program under the Marie Skodowska Curie grant agreement No. 813278 (A-WEAR: A network for dynamic wearable applications with privacy constraints).

Acknowledgments

The authors gratefully acknowledge funding from European Union’s Horizon 2020 Research and Innovation program under the Marie Skłodowska Curie grant agreement No. 813278 (A-WEAR: A network for dynamic wearable applications with privacy constraints, http://www.a-wear.eu/).

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

PDParkinson’s disease
QoLQuality of life
UPDRSUnified Parkinson’s disease rating scale
FOGFreezing of gait
DLADaily life activities
IMUInertial measurement unit
TUGTimed up and go

References

  1. Alzheimer’s Disease and Healthy Aging-Cognitive Impairment. 2020. Available online: https://www.cdc.gov/aging/pdf/cognitive_impairment/cogimp_poilicy_final.pdf (accessed on 25 January 2020).
  2. Strydom, A.; Fleisher, M.H.; Deb, S.; Ring, H.; Esralew, L.; Dodd, K.; al Janab, T.; Trollor, J.; Whitwham, S.L. Neurocognitive Disorders. Available online: https://www.ucl.ac.uk/intellectual-developmental-disabilities-research/sites/intellectual-developmental-disabilities-research/files/DMID-2_Neurocognitive_disorders.pdf (accessed on 9 May 2020).
  3. Durand, V.M.; Barlow, D.H. Essentials of Abnormal Psychology; Cengage Learning: Belmont, CA, USA, 2012. [Google Scholar]
  4. Naqvi, E. Parkinson’s Disease Statistics. 2020. Available online: https://parkinsonsnewstoday.com/parkinsons-disease-statistics/?fbclid=IwAR3_8-8t1AzNT510ObUf6IdZ9PcyLHj_A2XFIUQAifBAbsSGfrbGh1lzDe0 (accessed on 25 January 2020).
  5. Parkinson’s Disease. 2018. Available online: https://www.mayoclinic.org/diseases-conditions/parkinsons-disease/symptoms-causes/syc-20376055 (accessed on 25 January 2020).
  6. Chen, P.H.; Wang, R.L.; Liou, D.J.; Shaw, J.S. Gait disorders in Parkinson’s disease: Assessment and management. Int. J. Gerontol. 2013, 7, 189–193. [Google Scholar] [CrossRef] [Green Version]
  7. Lukšys, D.; Jonaitis, G.; Griškevičius, J. Quantitative analysis of parkinsonian tremor in a clinical setting using inertial measurement units. Park. Dis. 2018, 2018, 1683831. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Elble, R.J.; McNames, J. Using portable transducers to measure tremor severity. Tremor Other Hyperkinet. Mov. 2016, 6, 375. [Google Scholar]
  9. How Wearable Tech Can Help People with Parkinson’s Disease. 2019. Available online: https://www.apdaparkinson.org/article/wearable-technology-in-parkinsons/ (accessed on 25 January 2020).
  10. Godoi, B.B.; Amorim, G.D.; Quiroga, D.G.; Holanda, V.M.; Júlio, T.; Tournier, M.B. Parkinson’s disease and wearable devices, new perspectives for a public health issue: An integrative literature review. Rev. Assoc. Méd. Bras. 2019, 65, 1413–1420. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Baker, J.M. Gait disorders. Am. J. Med. 2018, 131, 602–607. [Google Scholar] [CrossRef] [PubMed]
  12. Son, H.; Park, W.S.; Kim, H. Mobility monitoring using smart technologies for Parkinson’s disease in free-living environment. Collegian 2018, 25, 549–560. [Google Scholar] [CrossRef]
  13. Rovini, E.; Maremmani, C.; Cavallo, F. How wearable sensors can support Parkinson’s disease diagnosis and treatment: A systematic review. Front. Neurosci. 2017, 11, 555. [Google Scholar] [CrossRef]
  14. Lan, K.C.; Shih, W.Y. Early Diagnosis of Parkinson’s Disease Using a Smartphone. Procedia Comput. Sci. 2014, 34, 305–312. [Google Scholar] [CrossRef] [Green Version]
  15. Margiotta, N.; Avitabile, G.; Coviello, G. A wearable wireless system for gait analysis for early diagnosis of Alzheimer and Parkinson disease. In Proceedings of the 2016 5th International Conference on Electronic Devices, Systems and Applications (ICEDSA), Ras Al Khaimah, UAE, 6–8 December 2016; pp. 1–4. [Google Scholar]
  16. Kim, H.B.; Lee, W.W.; Kim, A.; Lee, H.J.; Park, H.Y.; Jeon, H.S.; Kim, S.K.; Jeon, B.; Park, K.S. Wrist sensor-based tremor severity quantification in Parkinson’s disease using convolutional neural network. Comput. Biol. Med. 2018, 95, 140–146. [Google Scholar] [CrossRef]
  17. López-Blanco, R.; Velasco, M.A.; Méndez-Guerrero, A.; Romero, J.P.; Del Castillo, M.D.; Serrano, J.I.; Rocon, E.; Benito-León, J. Smartwatch for the analysis of rest tremor in patients with Parkinson’s disease. J. Neurol. Sci. 2019, 401, 37–42. [Google Scholar] [CrossRef]
  18. Memar, S.; Delrobaei, M.; Pieterman, M.; McIsaac, K.; Jog, M. Quantification of whole-body bradykinesia in Parkinson’s disease participants using multiple inertial sensors. J. Neurol. Sci. 2018, 387, 157–165. [Google Scholar] [CrossRef] [PubMed]
  19. Tsipouras, M.G.; Tzallas, A.T.; Karvounis, E.C.; Tsalikakis, D.G.; Cancela, J.; Pastorino, M.; Waldmeyer, M.T.A.; Konitsiotis, S.; Fotiadis, D.I. A wearable system for long-term ubiquitous monitoring of common motor symptoms in patients with Parkinson’s disease. In Proceedings of the IEEE-EMBS International Conference on Biomedical and Health Informatics (BHI), Valencia, Spain, 1–4 June 2014; pp. 173–176. [Google Scholar]
  20. Ginis, P.; Nieuwboer, A.; Dorfman, M.; Ferrari, A.; Gazit, E.; Canning, C.G.; Rocchi, L.; Chiari, L.; Hausdorff, J.M.; Mirelman, A. Feasibility and effects of home-based smartphone-delivered automated feedback training for gait in people with Parkinson’s disease: A pilot randomized controlled trial. Park. Relat. Disord. 2016, 22, 28–34. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Mariani, B.; Jiménez, M.C.; Vingerhoets, F.J.; Aminian, K. On-shoe wearable sensors for gait and turning assessment of patients with Parkinson’s disease. IEEE Trans. Biomed. Eng. 2012, 60, 155–158. [Google Scholar] [CrossRef] [PubMed]
  22. Hua, R.; Wang, Y. Monitoring Insole (MONI): A Low Power Solution Toward Daily Gait Monitoring and Analysis. IEEE Sens. J. 2019, 19, 6410–6420. [Google Scholar] [CrossRef]
  23. Delrobaei, M.; Memar, S.; Pieterman, M.; Stratton, T.W.; McIsaac, K.; Jog, M. Towards remote monitoring of Parkinson’s disease tremor using wearable motion capture systems. J. Neurol. Sci. 2018, 384, 38–45. [Google Scholar] [CrossRef] [Green Version]
  24. Mancini, M.; Bloem, B.R.; Horak, F.B.; Lewis, S.J.; Nieuwboer, A.; Nonnekes, J. Clinical and methodological challenges for assessing freezing of gait: Future perspectives. Mov. Disord. 2019, 34, 783–790. [Google Scholar] [CrossRef]
  25. Mazilu, S.; Calatroni, A.; Gazit, E.; Mirelman, A.; Hausdorff, J.M.; Tröster, G. Prediction of freezing of gait in Parkinson’s from physiological wearables: An exploratory study. IEEE J. Biomed. Health Inform. 2015, 19, 1843–1854. [Google Scholar] [CrossRef]
  26. Farahani, B.; Firouzi, F.; Chang, V.; Badaroglu, M.; Constant, N.; Mankodiya, K. Towards fog-driven IoT eHealth: Promises and challenges of IoT in medicine and healthcare. Future Gener. Comput. Syst. 2018, 78, 659–676. [Google Scholar] [CrossRef] [Green Version]
  27. Piau, A.; Wild, K.; Mattek, N.; Kaye, J. Current State of Digital Biomarker Technologies for Real-Life, Home-Based Monitoring of Cognitive Function for Mild Cognitive Impairment to Mild Alzheimer Disease and Implications for Clinical Care: Systematic Review. J. Med. Internet Res. 2019, 21, e12785. [Google Scholar] [CrossRef]
  28. Pasluosta, C.F.; Gassner, H.; Winkler, J.; Klucken, J.; Eskofier, B.M. An emerging era in the management of Parkinson’s disease: Wearable technologies and the internet of things. IEEE J. Biomed. Health Inform. 2015, 19, 1873–1881. [Google Scholar] [CrossRef]
  29. Heldman, D.A.; Giuffrida, J.P.; Cubo, E. Wearable sensors for advanced therapy referral in Parkinson’s disease. J. Park. Dis. 2016, 6, 631–638. [Google Scholar] [CrossRef] [PubMed]
  30. Ossig, C.; Antonini, A.; Buhmann, C.; Classen, J.; Csoti, I.; Falkenburger, B.; Schwarz, M.; Winkler, J.; Storch, A. Wearable sensor-based objective assessment of motor symptoms in Parkinson’s disease. J. Neural Transm. 2016, 123, 57–64. [Google Scholar] [CrossRef] [PubMed]
  31. Del Din, S.; Godfrey, A.; Mazzà, C.; Lord, S.; Rochester, L. Free-living monitoring of Parkinson’s disease: Lessons from the field. Mov. Disord. 2016, 31, 1293–1313. [Google Scholar] [CrossRef]
  32. Ramdhani, R.A.; Khojandi, A.; Shylo, O.; Kopell, B.H. Optimizing clinical assessments in Parkinson’s disease through the use of wearable sensors and data driven modeling. Front. Comput. Neurosci. 2018, 12, 72. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Sweeney, D.; Quinlan, L.R.; Browne, P.; Richardson, M.; Meskell, P.; ÓLaighin, G. A technological review of wearable cueing devices addressing freezing of gait in Parkinson’s disease. Sensors 2019, 19, 1277. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Ngueleu, A.M.; Blanchette, A.K.; Maltais, D.; Moffet, H.; McFadyen, B.J.; Bouyer, L.; Batcho, C.S. Validity of Instrumented Insoles for Step Counting, Posture and Activity Recognition: A Systematic Review. Sensors 2019, 19, 2438. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Rosevall, J.; Rusu, C.; Talavera, G.; Carrabina, J.; Garcia, J.; Carenas, C.; Breuil, F.; Reixach, E.; Torrent, M.; Burkard, S.; et al. A wireless sensor insole for collecting gait data. Stud. Heal. Technol. Inf. 2014, 200, 176–178. [Google Scholar]
  36. Hatton, A.L.; Dixon, J.; Rome, K.; Brauer, S.G.; Williams, K.; Kerr, G. The effects of prolonged wear of textured shoe insoles on gait, foot sensation and proprioception in people with multiple sclerosis: Study protocol for a randomised controlled trial. Trials 2016, 17, 208. [Google Scholar] [CrossRef] [Green Version]
  37. Han, Y.; Cao, Y.; Zhao, J.; Yin, Y.; Ye, L.; Wang, X.; You, Z. A self-powered insole for human motion recognition. Sensors 2016, 16, 1502. [Google Scholar] [CrossRef] [Green Version]
  38. Qiu, F.; Cole, M.H.; Davids, K.W.; Hennig, E.M.; Silburn, P.A.; Netscher, H.; Kerr, G.K. Effects of textured insoles on balance in people with Parkinson’s disease. PLoS ONE 2013, 8. [Google Scholar] [CrossRef] [Green Version]
  39. Mustufa, Y.A.; Barton, J.; O’Flynn, B.; Davies, R.; McCullagh, P.; Zheng, H. Design of a smart insole for ambulatory assessment of gait. In Proceedings of the 2015 IEEE 12th International Conference on Wearable and Implantable Body Sensor Networks (BSN), Cambridge, MA, USA, 9–12 June 2015; pp. 1–5. [Google Scholar]
  40. Hobert, M.A.; Maetzler, W.; Aminian, K.; Chiari, L. Technical and clinical view on ambulatory assessment in Parkinson’s disease. Acta Neurol. Scand. 2014, 130, 139–147. [Google Scholar] [CrossRef] [PubMed]
  41. Kubota, K.J.; Chen, J.A.; Little, M.A. Machine learning for large-scale wearable sensor data in Parkinson’s disease: Concepts, promises, pitfalls, and futures. Mov. Disord. 2016, 31, 1314–1326. [Google Scholar] [CrossRef] [PubMed]
  42. Figueiredo, J.; Santos, C.P.; Moreno, J.C. Automatic recognition of gait patterns in human motor disorders using machine learning: A review. Med. Eng. Phys. 2018, 53, 1–12. [Google Scholar] [CrossRef]
  43. Johansson, D.; Thomas, I.; Ericsson, A.; Johansson, A.; Medvedev, A.; Memedi, M.; Nyholm, D.; Ohlsson, F.; Senek, M.; Spira, J.; et al. Evaluation of a sensor algorithm for motor state rating in Parkinson’s disease. Park. Relat. Disord. 2019, 64, 112–117. [Google Scholar] [CrossRef] [PubMed]
  44. Capecci, M.; Pournajaf, S.; Galafate, D.; Sale, P.; Le Pera, D.; Goffredo, M.; De Pandis, M.F.; Andrenelli, E.; Pennacchioni, M.; Ceravolo, M.G.; et al. Clinical effects of robot-assisted gait training and treadmill training for Parkinson’s disease. A randomized controlled trial. Ann. Phys. Rehabil. Med. 2019, 62, 303–312. [Google Scholar] [CrossRef] [PubMed]
  45. Flynn, A.; Allen, N.E.; Dennis, S.; Canning, C.G.; Preston, E. Home-based prescribed exercise improves balance-related activities in people with Parkinson’s disease and has benefits similar to centre-based exercise: A systematic review. J. Physiother. 2019, 65, 189–199. [Google Scholar] [CrossRef] [PubMed]
  46. Gordt, K.; Gerhardy, T.; Najafi, B.; Schwenk, M. Effects of wearable sensor-based balance and gait training on balance, gait, and functional performance in healthy and patient populations: A systematic review and meta-analysis of randomized controlled trials. Gerontology 2018, 64, 74–89. [Google Scholar] [CrossRef]
  47. Raccagni, C.; Goebel, G.; Gaßner, H.; Granata, R.; Ndayisaba, J.P.; Seebacher, B.; Schoenherr, G.; Mitterhuber, J.; Hendriks, P.; Kaindlstorfer, C.; et al. Physiotherapy improves motor function in patients with the Parkinson variant of multiple system atrophy: A prospective trial. Park. Relat. Disord. 2019, 67, 60–65. [Google Scholar] [CrossRef]
  48. Hu, B.; Chomiak, T. Wearable technological platform for multidomain diagnostic and exercise interventions in Parkinson’s disease. Int. Rev. Neurobiol. 2019, 147, 75–93. [Google Scholar]
  49. Koop, M.M.; Rosenfeldt, A.B.; Alberts, J.L. Mobility improves after high intensity aerobic exercise in individuals with Parkinson’s disease. J. Neurol. Sci. 2019, 399, 187–193. [Google Scholar] [CrossRef]
  50. Carpinella, I.; Cattaneo, D.; Bonora, G.; Bowman, T.; Martina, L.; Montesano, A.; Ferrarin, M. Wearable sensor-based biofeedback training for balance and gait in Parkinson disease: A pilot randomized controlled trial. Arch. Phys. Med. Rehabil. 2017, 98, 622–630. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  51. Taghizadeh, G.; Azad, A.; Kashefi, S.; Fallah, S.; Daneshjoo, F. The effect of sensory-motor training on hand and upper extremity sensory and motor function in patients with idiopathic Parkinson disease. J. Hand Ther. 2018, 31, 486–493. [Google Scholar] [CrossRef] [PubMed]
  52. Mohammadi-Abdar, H.; Ridgel, A.L.; Discenzo, F.M.; Loparo, K.A. Design and development of a smart exercise bike for motor rehabilitation in individuals with Parkinson’s disease. IEEE/ASME Trans. Mechatron. 2015, 21, 1650–1658. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Heli, V.R.; Rauhala, A.; Fagerström, L. Person-centered home-based rehabilitation for persons with Parkinson’s disease–a scoping review. Int. J. Nurs. Stud. 2019, 103395. [Google Scholar] [CrossRef]
  54. Tosserams, A.; de Vries, N.M.; Bloem, B.R.; Nonnekes, J. Multidisciplinary Care to Optimize Functional Mobility in Parkinson Disease. Clin. Geriatr. Med. 2019, 36, 159–172. [Google Scholar] [CrossRef]
  55. Kleiner, A.F.R.; Pacifici, I.; Vagnini, A.; Camerota, F.; Celletti, C.; Stocchi, F.; De Pandis, M.F.; Galli, M. Timed up and go evaluation with wearable devices: Validation in Parkinson’s disease. J. Bodyw. Mov. Ther. 2018, 22, 390–395. [Google Scholar] [CrossRef]
  56. Simbaña, E.D.O.; Baeza, P.S.H.; Huete, A.J.; Balaguer, C. Review of automated systems for upper limbs functional assessment in neurorehabilitation. IEEE Access 2019, 7, 32352–32367. [Google Scholar] [CrossRef]
Figure 1. PRISMA adapted flow diagram used for the articles’ systematic selection.
Figure 1. PRISMA adapted flow diagram used for the articles’ systematic selection.
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Figure 2. Stages adopted for the systematic selection of articles.
Figure 2. Stages adopted for the systematic selection of articles.
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Figure 3. (a) shows Normal person gait and (b) shows PD patient gait.
Figure 3. (a) shows Normal person gait and (b) shows PD patient gait.
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Table 1. Numerical database search results.
Table 1. Numerical database search results.
Combination of KeywordsElsevierIEEE XplorerPubMedOther SourcesTotal
wearable sensors AND parkinson’s disorder86490145301129
wearable sensors AND neurocognitive disorder11602212150
parkinson patients AND rehabilitation exercises143132458601981
Total24111226251023260
Table 2. Step 2: Relevant articles after screening titles and abstracts.
Table 2. Step 2: Relevant articles after screening titles and abstracts.
ElsevierIEEE XplorerPubMedOther SourcesTotal
2819734220740
Table 3. Step 3: Relevant articles after screening of ISI Web of Science Indexing.
Table 3. Step 3: Relevant articles after screening of ISI Web of Science Indexing.
ElsevierIEEE XplorerPubMedOther SourcesTotal
2306433510639
Table 4. Scoring of Q3: Number of patients/subjects participated in the study.
Table 4. Scoring of Q3: Number of patients/subjects participated in the study.
No. of SubjectsQ3 Ranged (0–5)Q4 Ranged (0–1)
010.2
120.4
2–430.6
5–1040.8
>1051
Table 5. Scoring of Q4 in case of review articles.
Table 5. Scoring of Q4 in case of review articles.
No. of ReferencesQ4 Ranged (0–5)Q4 Ranged (0–1)
000
1–1010.2
11–2020.4
21–3030.6
31–4040.8
>4151
Table 6. Motor disabilities that affects Quality of Life (QoL).
Table 6. Motor disabilities that affects Quality of Life (QoL).
Motor DisabilitiesDescription
Shuffling gaitvery small fleeting steps and bent postures
Freezing of gaitepisodic absence in which feet are glued shut
Masked face (hypomimia)results from unification of Bradykinesia and rigidity
Balanceinability to maintain a steady and upright posture to prevent fall
Tremortwitching movements
Bradykinesiaslow movement
Dyskinesiaspontaneous, abnormal movements of the facial, arms, legs, or trunk
Festinationshortened and speedy steps taken during normal walking.
Rigidityinflexibility or stiffness of joints
Table 7. Wearable insoles models for diagnosis, monitoring, and rehabilitation.
Table 7. Wearable insoles models for diagnosis, monitoring, and rehabilitation.
First Author [Ref] YearTechnology DescriptionClinical Scoring SystemData Transmission MethodsSubjectsAlgorithmsFeaturesClinical Feature ActivityMain Results
Rosevall, J [35] 2014Pressure and Inertial Sensors (three-axis accelerometer and three-axis gyroscope). Comfortable, flexible, portable, and suitable for clinical and home settingFall efficacy scale(FES), modern falls efficacy scale (MFES) and UPDRS scaling1/2 wavelength dipole antenna and Bluetooth low energy14Pattern Recognition algorithmStride time, step length, foot clearance, and postural swayThe system analyses several gait parameters and finds patterns, markers and thresholds that differentiate between fallers and non-fallers.They measured the fall risk. Sensors are connected between a voltage supply level and a multiplexer that can be controlled to connect one sensor at a time to the input of a transimpedance amplifier which is read using an ADC on a microcontroller that can scan the pressure distribution up to 50 times per second. The standard deviation is of order 10%.
Hatton, Anna L. [36] 2016Smooth insoles and textured insoles worn for 14 weeks. Commercially available, inexpensive, non-invasive, and previously used in many research strategies.Multiple sclerosis walking scale (MSWS-29), MS QoL-54 and modified fatigue impact scaleNA176General linear models (repeated measures analysis of variance ANOVA)Stride length, stride time variability, double-limb support time, velocity, gait kinematics (hip, knee, and ankle joint angles, toe clearance, trunk inclination, arm swing, mediolateral pelvis), foot sensation (light touch-pressure, vibration, two-point discrimination) and proprioception (ankle joint position sense)The results of the study suggest that the textured effect is clinically significant, the study has the potential to identify a new, evidence-based footwear intervention which has the capacity to enhance mobility and independent living in people with multiple sclerosisThis study may generate vital evidence to inform the development of more effective, multi-faceted, and multi-disciplinary rehabilitation programs, for specific gait impairments
Han, Yingzhou [37] 2016Piezoelectric staves are inserted between the upper and lower plates on which there are wavy ribs and grooves. The force on upper plate is capable of recognizing different human movementsUPDRS, MDS-UPDRS and Unified Dyskinesia Rating Scale (UDysRS)NA3Own customized algorithmFeatures extracted from various kinds of voltage waveforms, which reflect variations in plantar pressure.Forefoot and heel strike features helps in distinguishing normal and abnormal gait parametersMonitor DLAs and the total accuracy is 93.33%, Self-detecting accuracy is 100%, and the non-self-detecting accuracy is 91.67%.
Qiu, Feng [38] 2013Textured insoles provide a passive intervention that is an inexpensive and accessible means to enhance the somatosensory input from the plantar surface of the feetUPDRS, MDS-UPDRS and Unified Dyskinesia Rating Scale (UDysRS)NA20 healthy and 20 patientsMixed model analysis of variance (ANOVA)Anterior posterior and medial lateral sway also standard deviationEffect of surface standing on the foam compared to the firm surfaces (F(1,78) = 208.885, p < 0.001) also effect of insoles (F(2,156) = 5.825, p = 0.004) and post-hoc comparisons with barefootML postural sway SD was greater for the PD participants compared with the control (F(1,78) = 13.165, p = 0.001). ML postural sway SD was not much different between the smooth and textured insoles (Fisher’s LSD: p = 0.127)
Mustufa, Ys Ashad [39] 2015Multi-layered rugged, low cost, scalable and durable packaged insoles. Developed with Piezoelectric, temperature, accelerometer and force sensorsTimed up and go test (TUG)Bluetooth communication protocol (LMX9834)NANAPlantar pressure, temperature, rotational angels of feetThe second phase will oversee the collection of a dataset for n = 10 healthy individuals which will be used to inform the generation of a key feature set.The system records the plantar pressure, temperature, acceleration, and the rotation angle of the foot to provide an unobtrusive and ubiquitous hardware.
Table 8. Rehabilitation exercises and assessment tests.
Table 8. Rehabilitation exercises and assessment tests.
First Author [Ref] YearExercise TypeSubjects/PatientsDurationEvaluation TestConclusions
Capecci, Mariana [44] 2019Robot assisted gait and Treadmill training (TT)Total 96 subjects (48 with robot assisted and 48 with treadmill training)20 sessions of 45 min gait training assisted by an end effector robot device (G-EO system or TT)6 min walking test, TUG test, FOG questionnaire, UPDRS QoL questionnaire-39 administered before To and T1.Results are better with robot assisted than TT
Flynn, Allyson [45] 2018Home based exercisePD subjects4 sessions over 2 weeksPooled based analysis as outcome of exercise also correlation of score with follow ups of post interventionRecovery in balance and gait speed with mild to moderate PD
Gordt, Katharina 2018 [46]Wireless sensor training: 1. static; 2. dynamic; 3. Proactive balance training8 randomized control trials (RCTs) were included1 day (1 session) to 8 weeks (15 sessions in total)Conventional balance training controls specific gait parameters and proactive balance measures.Better results with steady state balance
Raccagni C. [47] 2019PhysiotherapyGroup of 10 individuals of Parkinsonian variant of multiple system atrophy and 10 subjects with PD Hoehn and Yahr stage(<=3)5 day physiotherapy program followed by a 5-week unsupervised home based training.Questionnaires along with gait motion analysisResults are better with robot assisted than treadmill training
Hu, Bin [48] 2019Wearable technology300 patients17 monthsDetection of episodic gait freezing using Ambuloson during walking or steppingUPDRS scoring decreased by 0.3 points
Koop, Mandy Miller [49] 2019Aerobics59 patients with idiopathic PD8 week high intensive aerobic exerciseTUG testProgress in lower limb movements
Carpinella [50] 2017Wearable sensor based system named Gamepad operated as real time visual and acoustic feedback compared with physiotherapy42 PD subjects randomized into experimental and control group20 sessions training for balance and gait.Assessed by blinded examiner with a one-month follow up. In addition, considered Berg balance scale (BBS), 10 MWT and questionnairesGait improvements and enhanced transfer of training effects
Taghizadeh [51] 2018Sensory motor training (SMT) on hand and upper extremity sensory and motor function40 patients with PD for SMT10 sessions of SMT i.e., 5 days/week for 2 weeksPre- and post-testing sessions considering tactile acuity, proprioception, touch threshold, weight and texture discrimination, and haptic performance.SMT subjects with severity levels 1 to 3 of the Hoehn and Yahr scale showed progress in sensory and motor actions
Mohammadi- Abdar [52] 2015Smart bike47 ridersTwo algorithms that are static (inertial load) mode, or dynamic (speed reference) mode to collect data i.e., rider heart rate, cadence, and power at a high sampling rate.Clinical testsEffective tool in estimating the procure of new control paradigms for reforming the motor disabilities

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Channa, A.; Popescu, N.; Ciobanu, V. Wearable Solutions for Patients with Parkinson’s Disease and Neurocognitive Disorder: A Systematic Review. Sensors 2020, 20, 2713. https://doi.org/10.3390/s20092713

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Channa A, Popescu N, Ciobanu V. Wearable Solutions for Patients with Parkinson’s Disease and Neurocognitive Disorder: A Systematic Review. Sensors. 2020; 20(9):2713. https://doi.org/10.3390/s20092713

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Channa, Asma, Nirvana Popescu, and Vlad Ciobanu. 2020. "Wearable Solutions for Patients with Parkinson’s Disease and Neurocognitive Disorder: A Systematic Review" Sensors 20, no. 9: 2713. https://doi.org/10.3390/s20092713

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