Robot-Aided Motion Analysis in c: Comparison
Please note this is a comparison between Version 2 by Camila Xu and Version 1 by Mirjam Bonanno.

In the neurorehabilitation field, robot-aided motion analysis (R-AMA) could be helpful for two main reasons: (1) it allows the registration and monitoring of patients’ motion parameters in a more accurate way than clinical scales (clinical purpose), and (2) the multitude of data produced using R-AMA can be used to build machine learning algorithms, detecting prognostic and predictive factors for better motor outcomes (research purpose).

  • robot-aided motion analysis
  • objective motor assessment
  • biomechanics

1. Introduction

In the field of neurorehabilitation, innovative technologies, such as robotic devices, have been widely used to treat and evaluate patients affected by motor impairment due to different neurological disorders (e.g., stroke, multiple sclerosis (MS), and spinal cord injury (SCI)) [1]. Compared with conventional rehabilitation approaches, robotic-assisted therapy (RAT) may have some advantages, including (i) guaranteeing repetitive, intensive, and task-oriented rehabilitation; (ii) reducing the physical burden on clinical therapists, giving them the possibility to treat more patients simultaneously; and (iii) quantitatively and objectively assessing patients’ motor performance over time [2,3][2][3]. In particular, objective assessment of motor performance is a fundamental issue in neurorehabilitation [4]. In fact, clinical scales are still widely used in hospital settings, despite their validity and reliability being under debate. Robot-aided motion analysis (R-AMA) could be helpful for two main reasons: (i) it allows the registration and monitoring of patients’ motion parameters in a more accurate way than clinical scales (clinical purpose), and (ii) the multitude of data produced using R-AMA can be used to build machine learning algorithms, detecting prognostic and predictive factors for better motor outcomes (research purpose). Specifically, motion analysis refers to the recording of three-dimensional movements of human body segments and the subsequent computation of meaningful parameters that describe human movement from raw kinematic parameters [5,6][5][6]. Motion analysis is commonly carried out through wearable and non-wearable sensors that are able to detect biomechanical parameters of movements [7]. Similarly, robotic devices, both end effectors and exoskeletons, through specific sensors, could allow the detection of passive or active range of motion, movement accuracy, and planning [8]. For example, Maggioni et al. [9] examined the possibilities of assessing lower extremity function using robots, with parameters such as range of motion (RoM), muscle strength, and proprioception. In fact, the Lokomat (which is a tethered exoskeleton) was used to assess joint position sense (i.e., proprioception) in patients with incomplete spinal cord injury. Despite their potential in clinical settings, robotic assessment tools have not gained widespread clinical acceptance. Some barriers to and doubts about their clinical adoption remain, such as their reliability and validity compared to the existing standardized scales and motion analysis.

2. Motion Analysis and Its Biomechanical Contribution to Accuracy Prediction

Motion analysis involves registering the three-dimensional movements of human body segments and then calculating biomechanical parameters that describe human movement [11][10]. The modeling of human motion can be studied from different perspectives. For this purpose, various approaches are used to derive mathematical expressions that describe human motion. Newton’s equations of motion are the fundamental tools for understanding the cause–effect relationship between the forces acting on a system and the resulting motion [12][11]. However, applying them to complex systems, such as human locomotion, which involve a large number of degrees of freedom, requires formulating and solving multiple equations, leading to high computational costs. The Euler–Lagrange method is used in multibody systems because it analyzes the entire system without studying the reaction and contact forces between the elements that comprise the system. This equation allows for the study of human motion by focusing solely on the mechanical energy of the system. The knowledge of motion equations allows researchers to identify problems and design mechanisms that seek to recognize or recover human movements [13][12]. Nowadays, motion analysis has evolved substantially in parallel with technological advancements, encompassing various applications, such as clinical gait analysis and 3D biomechanical modeling [14][13]. Biomechanical motion analysis is generally based on two types of models: the multibody model and the finite element model. The first type consists of a set of rigid or flexible bodies connected by joints, while the second type of motion analysis reconstructs internal strain, stress, or deformation in flexible bodies based on continuum mechanics theories [15,16][14][15]. Within a rehabilitation setting, quantitative analysis of human body kinematics is a powerful tool that has been used to understand the different biomechanical patterns of both healthy and pathological individuals [17][16]. Recently, biomechanical tools have also been developed, ranging from simple manual annotation of images to marker-based optical trackers and inertial sensor-based systems. Nowadays, motion analysis can be performed using marker-less systems that use sophisticated human body models, computer vision, and machine learning algorithms [17][16]. Biomechanical parameters that are considered during motion analysis include kinematic and kinetic parameters [18,19][17][18]. In particular, kinematic parameters [20][19] include the spatial and temporal aspects of movement. These parameters describe (a) the “static” direction during point-to-point movements; (b) the continuous change of position, speed, and acceleration, which can be further subdivided into its amplitude and direction components; or (c) combinations of these, such as movement trajectories.

3. Robotic Devices for Upper Limb Measurement

Kinematic (e.g., position, velocity, and acceleration) and kinetic (e.g., force, joint torque, and muscle activity) data are acquired from sensors affixed to robotic and passive mechanical devices to measure biomechanical aspects of upper extremities [21,22,23,24,25,26,27,28][20][21][22][23][24][25][26][27] (see more in Table 1).
Table 1.
Studies about upper limb robotic-aided motion analysis performed in neurological disorders.
These kinds of measures are commonly registered in post-stroke patients, who may present unilateral hemiplegic involvement. However, the percentage of studies dealing with R-AMA for upper limbs is still poor. It seems that the Armeo®Spring was the most used for this issue, followed by the Armeo®Power, InMotion 2.0, and Gloreha Sinfonia, as reported in Figure 1.
Figure 1.
Percentage of selected articles reported in
Table 1
dealing with upper limb robotic-aided motion analysis.
For example, one of the most used robotic devices in post-stroke neurorehabilitation is the Armeo®Power, an exoskeleton for upper limb training. Its efficacy in improving functional outcomes is already demonstrated in the literature [34,35][33][34]; however, few authors have investigated its role in assessing upper limb functions. Specifically, this robotic device can evaluate specific kinematic parameters [36][35], as reported in Table 1. In addition, the Armeo®Power evaluates the range of joint movement, which is expressed in degrees, and the force of muscles, which is expressed in Newton meters (Nm). According to Galeoto et al. [29][28], the Armeo®Power can be considered an objective robotic tool compared to the Fugl–Meyer for upper limb (FM-UL) clinical scale items. The FM-UL clinical scale is the most used and reliable scale to assess motor functions, joint range of motion, joint pain, dysmetria, and tremor in post-stroke patients [37][36]. The authors found strong correlations between flexion synergy (forearm supination and elbow flexion) and results measured with the Armeo®Power. This suggests that the Armeo®Power is more accurate than the FM-UL clinical scale in evaluating upper limb movements [29][28]. Other researchers have also evaluated the motor function of stroke patients using robotic devices and measuring upper limb biomechanical features, such as movement velocity, accuracy, and smoothness in active training [30,31][29][30]. Merlo et al. [30][29] used the Armeo®Spring to conduct these measurements. To obtain objective data on upper limb functions, the Armeo®Spring calculates a set of numerical indices based on the 3D endpoint trajectory during the “vertical capture” task. The patient receives visual feedback of their hand position through a display, which is used to facilitate rehabilitation exercises. Indeed, the derived indices (movement velocity, accuracy, and smoothness) are easy to share with clinicians because they describe the motor impairment of the upper limb [28][27]. For example, the loss of movement accuracy can be related to a reduction in sensibility, whereas the decrease in velocity refers to paresis/paralysis, and the loss of smoothness refers to an abnormal muscle tone (spasticity) [38][37]. However, before implementing them in clinical practice, these indices must be validated by comparing them with other clinical scales. In their study, Longhi et al. [31][30] analyzed three aspects of upper limb (UL) evaluation. First, they examined the ability of the Armeo®Spring to distinguish between stroke patients and healthy subjects. Second, they assessed the validity of the indices used to measure movement. Lastly, they investigated the concurrent validity of these indices by comparing them with the Wolf Motor Function test, a clinically validated scale for assessing UL motor function. The authors’ results confirmed the construct validity of the three indices, which is consistent with the findings of Merlo et al. [30][29]. This suggests that the Armeo®Spring can be a promising tool for objectively assessing UL motor skills. In addition, Goffredo et al. [32][31] performed a kinematic evaluation of the upper limb in post-stroke patients using the end effector InMotion 2.0. The kinematic parameters were calculated from the trajectories recorded by the robot, starting from the central target and extending to the peripheral targets in various directions. The kinematic parameters described by the authors [32][31] refer to the functional abilities of the UL. However, the Armeo®Power and the Armeo®Spring cannot perform hand motion analysis due to their biomechanical architecture. To this aim, Cordella et al. [33][32] conducted a quantitative and objective assessment of hand movement in post-stroke patients using the Gloreha Sinfonia. The Gloreha Sinfonia is a robotic glove used to train hand motor functions, focusing on the recovery of range of motion [33][32]. Once calibrated, this glove allows an objective assessment of motor performance. In particular, the results of the authors [33][32] demonstrated that the Gloreha Sinfonia can measure angular values from bending sensors embedded in the glove. Another concern that should be considered in clinical practice is the objective evaluation of spasticity. The Modified Ashworth Scale (MAS) is, in fact, the most commonly used clinical tool for assessing spasticity. However, it does have several limitations [39][38]. Indeed, de-la-Torre et al. [38][37] in their systematic review found that R-AMA based on data capture is effective for evaluating spasticity. However, it should be noted that cutting-edge algorithms provide a more predictive and analytical measure than the only variation between the original and the final status obtained from clinical scales [38][37]. Moreover, some authors [40][39] have evaluated muscle synergies in post-stroke patients using a robotic device. Muscle synergy specifically refers to the coordinated activation of both joints and muscles in order to execute purposeful movements [41,42][40][41]. Post-stroke patients tend to activate abnormal muscle synergies due to brain lesions in the corticospinal tract, which are further enhanced by hyperreflexia. This aspect is fundamental in establishing the most effective treatment for patients in the clinical rehabilitation setting. In this vein, Kung et al. [40][39] found that robotic devices, such as end effectors, can be used for long-term evaluation of muscle synergies. They registered kinematic, kinetic, and electromyographic (EMG) signals during the tracking movement in order to develop biomechanical indices for evaluating muscle synergies. In fact, their results revealed that abnormal synergies can be assessed through two tracking directions: D2 (contra-proximal to ipsi-lateral) and D4 (left–right) [40][39]. Lastly, robotic devices can also measure muscle strength, as suggested by Toigo et al. [43][42]. In particular, the term “muscle strength” refers to force, moment, or power [43][42]. Robotic devices, including exoskeletons and end effectors, are equipped with force sensors for quantifying the interaction forces between the device and the patient [44][43]. These devices record raw sensor data on force during functional movements, enabling the extraction of valuable data detecting abnormal muscle synergies [43][42]. However, misalignments with the device and variations in the rotational axis of a joint can distort the results. Moreover, all kinematic and kinetic movement parameters are represented to some extent in the sensorimotor cortex. Distal movements of the hand, including movement direction and trajectories, can be discriminated in the sensorimotor cortex. This ability has potential applications in brain–computer interface technology [21][20].

4. Robotic Device for Lower Limb Assessment

Walking recovery in neurological patients is one of the most important goals planned by therapists [45][44]. In order to maximize the recovery of the walking function, it is important to define a personalized rehabilitation treatment, in addition to an accurate assessment to monitor patients’ progress. In fact, both clinical and instrumental tools already exist to perform an accurate analysis of motion [45][44]. However, if the assessment protocol takes too much time to perform, clinicians and therapists may be reluctant to adopt them. A possible solution could involve the use of robotic devices in which the patient would undergo both training and assessment. In this study, Imoto et al. [46][45] used a novel gait training robot known as WelWalk WW-2000. This robot enables the adjustment of various gait parameters (such as time and mechanical assistance load) during the training session. The robot is equipped with sensors and a markerless motion capture system to detect altered gait patterns in stroke patients. This system can evaluate individuals’ gait patterns and provide tailored rehabilitation gait training [46][45]. Generally, the objective assessment of the lower limb should consider the simultaneous measurement of joint angles, spatial and temporal parameters of gait, muscle strength, proprioception, and spasticity and/or muscle stiffness [47][46] (see Table 2).
Table 2.
Studies about lower limb robotic-aided motion analysis performed on neurological patients.
The Lokomat, which is a tethered exoskeleton, is one of most used robotic devices for gait training and for motion analysis in neurological disorders. In fact, 57% of the selected papers reported the use of the Lokomat in performing R-AMA, followed by Ekso and the WelWalk, as reported in Figure 2.
Figure 2.
Percentage of selected articles reported in
Table 2
dealing with lower limb robotic-aided motion analysis.
According to a systematic review [53][52], the Lokomat seems to be most suitable for the motion analysis of lower limbs. Maggioni et al. [54][53] used the Lokomat to perform a type of gait analysis, also adding force sensors and potentiometers. The authors successfully developed and tested a novel specific algorithm to assess walking through the Lokomat. Indeed, the Lokomat was used to calculate joint angles, assuming that those measured by the exoskeleton also corresponded to the human angles [54][53]. Mercado et al. [55][54] calculated joint angles in healthy subjects using the Denavit–Hartenberg notation and the Euler–Lagrange approach to process video recordings of movement. Another study [48][47] investigates the use of Ekso-GT, an overground exoskeleton, to assess gait parameters, such as stride time, stride length, gait speed, and gait events. Although Ekso does not provide a comprehensive report of gait parameters, these parameters and measurements can be derived from other calculations made by the exoskeleton. This allows for an accurate assessment of gait during training using mathematical models. In addition, exoskeletons, like Ekso, can be integrated with surface electromyography (sEMG) signals to monitor muscle synergies and muscular patterns during walking. According to a systematic review [56][55], the rectus femoris and vastus lateralis are the most frequently recorded muscles during gait. Indeed, the posterior calf muscles, which play a role in ankle and foot movement, have been less studied during gait training, despite their importance in the gait cycle. Similarly, Afzal et al. [49][48] investigated muscle synergies in patients with MS who were wearing an exoskeleton. EMG signals were recorded from seven muscles, including the vastus medialis, rectus femoris, biceps femoris, semitendinosus, soleus, medial gastrocnemius, and tibialis anterior muscles. The authors demonstrated that exoskeleton assistance does not alter the existing muscle synergies but it can induce a modification in neural commands [49][48]. Another point to consider is the evaluation of proprioception provided by robotic devices. Three studies [50,51,52][49][50][51] in spinal cord patients have addressed the evaluation of proprioception or kinesthesia using the Lokomat. In fact, the Lokomat is equipped with position sensors that are able to determine joint angles. For proprioception, the authors considered the difference between the target position and the achieved position for evaluation purposes [50,51][49][50]. Another author [52][51] evaluated kinesthesia by passively moving the lower limb in a specific direction while patients were wearing the exoskeleton.

References

  1. Iandolo, R.; Marini, F.; Semprini, M.; Laffranchi, M.; Mugnosso, M.; Cherif, A.; De Michieli, L.; Chiappalone, M.; Zenzeri, J. Perspectives and Challenges in Robotic Neurorehabilitation. Appl. Sci. 2019, 9, 3183.
  2. Meng, W.; Liu, Q.; Zhou, Z.; Ai, Q.; Sheng, B.; Xie, S. Recent development of mechanisms and control strategies for robot-assisted lower limb rehabilitation. Mechatronics 2015, 31, 132–145.
  3. Rehmat, N.; Zuo, J.; Meng, W.; Liu, Q.; Xie, S.Q.; Liang, H. Upper limb rehabilitation using robotic exoskeleton systems: A systematic review. Int. J. Intell. Robot. Appl. 2018, 2, 283–295.
  4. Shishov, N.; Melzer, I.; Bar-Haim, S. Parameters and Measures in Assessment of Motor Learning in Neurorehabilitation; A Systematic Review of the Literature. Front. Hum. Neurosci. 2017, 11, 82.
  5. Roggio, F.; Ravalli, S.; Maugeri, G.; Bianco, A.; Palma, A.; Di Rosa, M.; Musumeci, G. Technological advancements in the analysis of human motion and posture management through digital devices. World J. Orthop. 2021, 12, 467–484.
  6. Crenna, F.; Rossi, G.B.; Berardengo, M. Filtering Biomechanical Signals in Movement Analysis. Sensors 2021, 21, 4580.
  7. Muro-de-la-Herran, A.; Garcia-Zapirain, B.; Mendez-Zorrilla, A. Gait analysis methods: An overview of wearable and non-wearable systems, highlighting clinical applications. Sensors 2014, 14, 3362–3394.
  8. Laut, J.; Porfiri, M.; Raghavan, P. The Present and Future of Robotic Technology in Rehabilitation. Curr. Phys. Med. Rehabil. Rep. 2016, 4, 312–319.
  9. Maggioni, S.; Melendez-Calderon, A.; van Asseldonk, E.; Klamroth-Marganska, V.; Lünenburger, L.; Riener, R.; van der Kooij, H. Robot-aided assessment of lower extremity functions: A review. J. Neuroeng. Rehabil. 2016, 13, 72.
  10. Ma, C.Z.-H.; Li, Z.; He, C. Advances in Biomechanics-Based Motion Analysis. Bioengineering 2023, 10, 677.
  11. Grimmer, M.; Zeiss, J.; Weigand, F.; Zhao, G.; Lamm, S.; Steil, M.; Heller, A. Lower limb joint biomechanics-based identification of gait transitions in between level walking and stair ambulation. PLoS ONE 2020, 15, e0239148.
  12. Sugihara, T.; Fujimoto, Y. Dynamics Analysis: Equations of Motion. In Humanoid Robotics: A Reference; Goswami, A., Vadakkepat, P., Eds.; Springer: Dordrecht, The Netherlands, 2017.
  13. Yeadon, M.; Pain, M. Fifty years of performance-related sports biomechanics research. J. Biomech. 2023, 155, 111666.
  14. Lerchl, T.; Nispel, K.; Baum, T.; Bodden, J.; Senner, V.; Kirschke, J.S. Multibody Models of the Thoracolumbar Spine: A Review on Applications, Limitations, and Challenges. Bioengineering 2023, 10, 202.
  15. Parashar, S.K.; Sharma, J.K. A review on application of finite element modelling in bone biomechanics. Perspect. Sci. 2016, 8, 696–698.
  16. Colyer, S.L.; Evans, M.; Cosker, D.P.; Salo, A.I.T. A Review of the Evolution of Vision-Based Motion Analysis and the Integration of Advanced Computer Vision Methods towards Developing a Markerless System. Sports Med.-Open 2018, 4, 24.
  17. Kwon, C.-W.; Yun, S.-H.; Koo, D.-K.; Kwon, J.-W. Kinetic and Kinematic Analysis of Gait Termination: A Comparison between Planned and Unplanned Conditions. Appl. Sci. 2023, 13, 7323.
  18. Aprile, I.; Rabuffetti, M.; Padua, L.; Di Sipio, E.; Simbolotti, C.; Ferrarin, M. Kinematic Analysis of the Upper Limb Motor Strategies in Stroke Patients as a Tool towards Advanced Neurorehabilitation Strategies: A Preliminary Study. BioMed Res. Int. 2014, 2014, 636123.
  19. Brihmat, N.; Loubinoux, I.; Castel-Lacanal, E.; Marque, P.; Gasq, D. Kinematic parameters obtained with the ArmeoSpring for upper-limb assessment after stroke: A reliability and learning effect study for guiding parameter use. J. Neuroeng. Rehabil. 2020, 17, 130.
  20. Branco, M.P.; de Boer, L.M.; Ramsey, N.F.; Vansteensel, M.J. Encoding of kinetic and kinematic movement parameters in the sensorimotor cortex: A Brain-Computer Interface perspective. Eur. J. Neurosci. 2019, 50, 2755–2772.
  21. Al-Mulla, M.R.; Sepulveda, F.; Colley, M. A Review of Non-Invasive Techniques to Detect and Predict Localised Muscle Fatigue. Sensors 2011, 11, 3545–3594.
  22. Schaefer, L.V.; Bittmann, F.N. Are there two forms of isometric muscle action? Results of the experimental study support a distinction between a holding and a pushing isometric muscle function. BMC Sports Sci. Med. Rehabil. 2017, 9, 11.
  23. Halilaj, E.; Rajagopal, A.; Fiterau, M.; Hicks, J.L.; Hastie, T.J.; Delp, S.L. Machine learning in human movement biomechanics: Best practices, common pitfalls, and new opportunities. J. Biomech. 2018, 81, 1–11.
  24. Giarmatzis, G.; Zacharaki, E.I.; Moustakas, K. Real-Time Prediction of Joint Forces by Motion Capture and Machine Learning. Sensors 2020, 20, 6933.
  25. Mundt, M.; Koeppe, A.; Bamer, F.; David, S.; Markert, B. Artificial Neural Networks in Motion Analysis—Applications of Unsupervised and Heuristic Feature Selection Techniques. Sensors 2020, 20, 4581.
  26. Ai, Q.; Liu, Z.; Meng, W.; Liu, Q.; Xie, S.Q. Machine Learning in Robot Assisted Upper Limb Rehabilitation: A Focused Review. IEEE Trans. Cogn. Dev. Syst. 2021.
  27. Maura, R.M.; Parra, S.R.; Stevens, R.E.; Weeks, D.L.; Wolbrecht, E.T.; Perry, J.C. Literature review of stroke assessment for upper-extremity physical function via EEG, EMG, kinematic, and kinetic measurements and their reliability. J. Neuroeng. Rehabil. 2023, 20, 21.
  28. Galeoto, G.; Berardi, A.; Mangone, M.; Tufo, L.; Silvani, M.; González-Bernal, J.; Seco-Calvo, J. Assessment Capacity of the Armeo® Power: Cross-Sectional Study. Technologies 2023, 11, 125.
  29. Merlo, A.; Longhi, M.; Giannotti, E.; Prati, P.; Giacobbi, M.; Ruscelli, E.; Mancini, A.; Ottaviani, M.; Montanari, L.; Mazzoli, D. Upper limb evaluation with robotic exoskeleton. Normative values for indices of accuracy, speed and smoothness. NeuroRehabilitation 2013, 33, 523–530.
  30. Longhi, M.; Merlo, A.; Prati, P.; Giacobbi, M.; Mazzoli, D. Instrumental indices for upper limb function assessment in stroke patients: A validation study. J. Neuroeng. Rehabil. 2016, 13, 52.
  31. Goffredo, M.; Pournajaf, S.; Proietti, S.; Gison, A.; Posteraro, F.; Franceschini, M. Retrospective Robot-Measured Upper Limb Kinematic Data From Stroke Patients Are Novel Biomarkers. Front. Neurol. 2021, 12, 803901.
  32. Cordella, F.; Scotto, D.; Luzio, F.; Bravi, M.; Santacaterina, F.; Bressi, F.; Zollo, L. Hand motion analysis during robot-aided rehabilitation in chronic stroke. J. Biol. Regul. Homeost. Agents 2020, 34 (Suppl. S3), 45–52.
  33. Calabrò, R.S.; Russo, M.; Naro, A.; Milardi, D.; Balletta, T.; Leo, A.; Filoni, S.; Bramanti, P. Who May Benefit From Armeo Power Treatment? A Neurophysiological Approach to Predict Neurorehabilitation Outcomes. PM&R 2016, 8, 971–978.
  34. Calabrò, R.S.; Naro, A.; Russo, M.; Milardi, D.; Leo, A.; Filoni, S.; Trinchera, A.; Bramanti, P. Is two better than one? Muscle vibration plus robotic rehabilitation to improve upper limb spasticity and function: A pilot randomized controlled trial. PLoS ONE 2017, 12, e0185936.
  35. Palermo, E.; Hayes, D.R.; Russo, E.F.; Calabrò, R.S.; Pacilli, A.; Filoni, S. Translational effects of robot-mediated therapy in subacute stroke patients: An experimental evaluation of upper limb motor recovery. PeerJ 2018, 6, e5544.
  36. Santisteban, L.; Térémetz, M.; Bleton, J.-P.; Baron, J.-C.; Maier, M.A.; Lindberg, P.G. Upper Limb Outcome Measures Used in Stroke Rehabilitation Studies: A Systematic Literature Review. PLoS ONE 2016, 11, e0154792.
  37. De-La-Torre, R.; Oña, E.D.; Balaguer, C.; Jardón, A. Robot-Aided Systems for Improving the Assessment of Upper Limb Spasticity: A Systematic Review. Sensors 2020, 20, 5251.
  38. Bonanno, M.; De Luca, R.; Torregrossa, W.; Tonin, P.; Calabrò, R.S. Moving toward Appropriate Motor Assessment Tools in People Affected by Severe Acquired Brain Injury: A Scoping Review with Clinical Advices. Healthcare 2022, 10, 1115.
  39. Kung, P.-C.; Lin, C.-C.K.; Ju, M.-S. Neuro-rehabilitation robot-assisted assessments of synergy patterns of forearm, elbow and shoulder joints in chronic stroke patients. Clin. Biomech. 2010, 25, 647–654.
  40. Zhao, K.; Zhang, Z.; Wen, H.; Liu, B.; Li, J.; D’avella, A.; Scano, A. Muscle synergies for evaluating upper limb in clinical applications: A systematic review. Heliyon 2023, 9, e16202.
  41. Safavynia, S.A.; Torres-Oviedo, G.; Ting, L.H. Muscle Synergies: Implications for Clinical Evaluation and Rehabilitation of Movement. Top. Spinal Cord Inj. Rehabil. 2011, 17, 16–24.
  42. Toigo, M.; Flück, M.; Riener, R.; Klamroth-Marganska, V. Robot-assisted assessment of muscle strength. J. Neuroeng. Rehabil. 2017, 14, 103.
  43. Tiboni, M.; Borboni, A.; Vérité, F.; Bregoli, C.; Amici, C. Sensors and Actuation Technologies in Exoskeletons: A Review. Sensors 2022, 22, 884.
  44. Bonanno, M.; De Nunzio, A.M.; Quartarone, A.; Militi, A.; Petralito, F.; Calabrò, R.S. Gait Analysis in Neurorehabilitation: From Research to Clinical Practice. Bioengineering 2023, 10, 785.
  45. Imoto, D.; Hirano, S.; Mukaino, M.; Saitoh, E.; Otaka, Y. A novel gait analysis system for detecting abnormal hemiparetic gait patterns during robot-assisted gait training: A criterion validity study among healthy adults. Front. Neurorobot. 2022, 16, 1047376.
  46. Boudarham, J.; Hameau, S.; Zory, R.; Hardy, A.; Bensmail, D.; Roche, N. Coactivation of Lower Limb Muscles during Gait in Patients with Multiple Sclerosis. PLoS ONE 2016, 11, e0158267.
  47. Romanato, M.; Spolaor, F.; Beretta, C.; Fichera, F.; Bertoldo, A.; Volpe, D.; Sawacha, Z. Quantitative assessment of training effects using EksoGT® exoskeleton in Parkinson’s disease patients: A randomized single blind clinical trial. Contemp. Clin. Trials Commun. 2022, 28, 100926.
  48. Afzal, T.; Zhu, F.; Tseng, S.-C.; Lincoln, J.A.; Francisco, G.E.; Su, H.; Chang, S.-H. Evaluation of Muscle Synergy During Exoskeleton-Assisted Walking in Persons With Multiple Sclerosis. IEEE Trans. Biomed. Eng. 2022, 69, 3265–3274.
  49. Domingo, A.; Marriott, E.; de Grave, R.B.; Lam, T. Quantifying lower limb joint position sense using a robotic exoskeleton: A pilot study. In Proceedings of the 2011 IEEE 12th International Conference on Rehabilitation Robotics: Reaching Users & the Community (ICORR 2011), Zurich, Switzerland, 29 June–1 July 2011; pp. 1–6.
  50. Domingo, A.; Lam, T. Reliability and validity of using the Lokomat to assess lower limb joint position sense in people with incomplete spinal cord injury. J. Neuroeng. Rehabil. 2014, 11, 167.
  51. Chisholm, A.E.; Domingo, A.; Jeyasurya, J.; Lam, T. Quantification of Lower Extremity Kinesthesia Deficits Using a Robotic Exoskeleton in People With a Spinal Cord Injury. Neurorehabilit. Neural Repair 2016, 30, 199–208.
  52. Moeller, T.; Moehler, F.; Krell-Roesch, J.; Dežman, M.; Marquardt, C.; Asfour, T.; Stein, T.; Woll, A. Use of Lower Limb Exoskeletons as an Assessment Tool for Human Motor Performance: A Systematic Review. Sensors 2023, 23, 3032.
  53. Maggioni, S.; Lunenburger, L.; Riener, R.; Melendez-Calderon, A. Robot-aided assessment of walking function based on an adaptive algorithm. In Proceedings of the 2015 IEEE International Conference on Rehabilitation Robotics (ICORR 2015), Singapore, 11–14 August 2015; Yu, H., Ed.; IEEE: Piscataway, NJ, USA, 2015; pp. 804–809, ISBN 978-1-4799-1808-9.
  54. Mercado, L.; Alvarado, L.; Quiroz-Compean, G.; Romo-Vazquez, R.; Vélez-Pérez, H.; Platas-Garza, M.; González-Garrido, A.A.; Gómez-Correa, J.; Morales, J.A.; Rodriguez-Liñan, A.; et al. Decoding the torque of lower limb joints from EEG recordings of pre-gait movements using a machine learning scheme. Neurocomputing 2021, 446, 118–129.
  55. El Yaakoubi, N.A.; McDonald, C.; Lennon, O. Prediction of Gait Kinematics and Kinetics: A Systematic Review of EMG and EEG Signal Use and Their Contribution to Prediction Accuracy. Bioengineering 2023, 10, 1162.
More
Video Production Service