Next Article in Journal
Sensing with Thermally Reduced Graphene Oxide under Repeated Large Multi-Directional Strain
Previous Article in Journal
Optimizing Automated Optical Inspection: An Adaptive Fusion and Semi-Supervised Self-Learning Approach for Elevated Accuracy and Efficiency in Scenarios with Scarce Labeled Data
Previous Article in Special Issue
Precision Balance Assessment in Parkinson’s Disease: Utilizing Vision-Based 3D Pose Tracking for Pull Test Analysis
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Communication

The Kinematic and Electromyographic Analysis of Roller Skating at Different Speeds on a Treadmill: A Case Study

1
Physiotherapy Department, Friuli Riabilitazione, 33080 Roveredo in Piano, Italy
2
IRCCS C.R.O. National Cancer Institute of Aviano, 33081 Aviano, Italy
3
Department of Management, Ca’ Foscari University of Venice, 30121 Venice, Italy
4
Collegium Medicum, University of Social Sciences, 90-229 Lodz, Poland
5
Department of Economics, Ca’ Foscari University of Venice, 30121 Venice, Italy
6
Department of Occupational and Environmental Medicine, Epidemiology and Hygiene, INAIL, Monte Porzio Catone, 00078 Rome, Italy
7
CeRiSM, Sport Mountain and Health Research Center, University of Verona, 38068 Rovereto, Italy
8
Department of Engineering for Innovation Medicine, University of Verona, 37134 Verona, Italy
9
Department of Pain Medicine, IRCCS C.R.O. National Cancer Institute of Aviano, 33081 Aviano, Italy
*
Author to whom correspondence should be addressed.
Sensors 2024, 24(17), 5738; https://doi.org/10.3390/s24175738
Submission received: 31 July 2024 / Revised: 27 August 2024 / Accepted: 30 August 2024 / Published: 4 September 2024
(This article belongs to the Special Issue Wearable Sensors for Monitoring Athletic and Clinical Cohorts)

Abstract

:
Elite athletes in speed roller skates perceive skating to be a more demanding exercise for the groin when compared to other cyclic disciplines, increasing their risk of injury. The objective of this study was to monitor the kinematic and electromyographic parameters of roller speed skaters, linearly, on a treadmill, and to compare different skating speeds, one at 20 km/h and one at 32 km/h, at a 1° inclination. The acquisition was carried out by placing an inertial sensor at the level of the first sacral vertebra, and eight surface electromyographic probes on both lower limbs. The kinematic and electromyographic analysis on the treadmill showed that a higher speed requires more muscle activation, in terms of maximum and average values and co-activation, as it not only increases the intrinsic muscle demand in the district, but also the athlete’s ability to coordinate the skating technique. The present study allows us to indicate not only how individual muscle districts are activated during skating on a surface different from the road, but also how different speeds affect the overall district load distributions concerning effective force, which is essential for the physiotherapist and kinesiologist for preventive and conditional purposes, while also considering possible variations in the skating technique in linear advancement.

1. Introduction

With its parallels to field hockey and ice skating, speed roller skating is a cyclic sport in which the active and passive locomotor apparatus is subjected to significant stress. The groin region has been found to be the most vulnerable to the injuries seen in these sports in the scientific literature. For instance, it has been shown that in field hockey, about 10% of injuries affect the groin district in acute or chronic conditions [1,2]. Furthermore, within a sport season, about 20% of professional athletes have suffered an injury not induced by traumatic events, but by overload or incorrect technique during performance, with significant consequences on their seasonal performance [3,4].
Studies conducted on field hockey, and recently on speed roller skating, show that the most engaged muscles are the gluteus major, the gluteus medius, and the vastus lateralis, which are active during the propulsion phase, through maximal hip and knee extension, along with the same abduction and extra rotation [5]. Furthermore, the posterior thigh districts are most active during the maximum gliding phase, through isometric contraction, to stabilize the knee joint with the respective coactivation of the knee extensors [6]. Regarding skating, the activity of the leg districts implies a large activation of the anterior tibialis during both the final phases of propulsion and the recovery induced by the ankle being forced into dorsal flexion [7].
Analyzing skating performed on a treadmill may be useful for monitoring multiple muscle behaviors, which could help movement therapists in post-injury rehabilitation and athletic reconditioning. To date, the discipline that most observes the differences between road surfaces and treadmills, in terms of ground impact, joint loading, biomechanics, district acceleration, and the usefulness of the conveyor belt for rehabilitation and reconditioning purposes, purely concerns ground running activity [8,9].
To the best of our knowledge, there are no studies on the kinematics and sEMG analysis of skating on a treadmill, so the present study results in the first evaluative and comparative framework carried out in this context.
However, there is a marked difference here to the cyclic pattern of running, in that the propulsive action of skating focuses on a very pronounced abduction of the lower limb.
This movement is particularly evident at the hip, with propulsion being achieved by the extension, abduction, and external rotation of the entire lower district [10].
To better understand the muscle activation on both roads and treadmills, it has been seen that the greatest load at the adductor is induced by the purely eccentric cyclic action that forces the limb to decelerate during the propulsive phase of skating [11,12].
In this study, we aim to perform an electromyographic and kinematic analysis of a professional athlete on a treadmill at two speeds to understand changes in terms of muscle activations and coactivations and kinematics, which may, in the long run, affect the onset of overload issues. To do this, we also analyzed the propulsion and recovery phases of the lower limb districts and the body accelerations through the entire cycle. This would allow us to verify both the muscular and coordination requirements of the skating athlete. The programming of this discipline must, in fact, take into consideration how the values acquired in kinematics and muscle activation change during higher speeds. This is the basic concept on which these athletes’ preventive and conditional foundation is based, subjected not only to high speeds, but also to how these can influence their skating technique overall.

2. Materials and Methods

2.1. Participant

The participant is an elite female athlete (30 years old, body weight of 50 kg, and stature of 160 cm), and a former Italian, European, and world champion in speed roller skating. She is a right-handed person. She is in good health, with no musculotendinous, joint, or other clinical pathologies.

2.2. Electromyographic and Inertial Measurement Unit Recordings

Surface myoelectric signals were acquired (sampling rate of 1000 Hz) using a 16-channel Wi-Fi transmission surface electromyograph (FreeEMG300 System, BTS, Milan, Italy). Bipolar Ag/AgCl surface electrodes (24 mm diameter, H124SG Kendall ARBO, Tyco Healthcare, Neustadt/Donau, Germany) prepared with electroconductive gel were placed over each muscle [13]. Bipolar electrodes were placed bilaterally on the soleus (SOL), tibialis anterior (TA), rectus femoris (RF), biceps femoris (BF), gluteus maximus (GMax), gluteus medius (GMed), adductor longus (AL), and vastus lateralis (VL). In the region of electrode application, the skin was shaved, lightly scrubbed with sandpaper, and cleaned with alcohol.
A triaxial accelerometer (200 Hz, G sensor, BTS Bioengineering, Corp., Garbagnate Milanese, Italy) was positioned at the S1 level of the participant, medially, and fixed by means of the supplied adjustable strap.

2.3. Experimental Procedures

The participant performed the following specific exercises [14] that were needed to record the muscle activity during the isometric maximum voluntary contractions (iMVCs) for each of the muscles investigated:
(1)
Push against a wall while standing on the sole of the foot;
(2)
Dorsal flexion of the foot while sitting with manual resistance;
(3)
Knee extension while sitting with fixed tibia;
(4)
Knee flexion in a prone position with manual resistance;
(5)
Hip flexion against manual resistance in a supine position;
(6)
Hip extension in a prone position;
(7)
Hip abduction against manual resistance in a supine position;
(8)
Hip adduction in a semi-sitting position against a foam roller tented between the thighs.
The recorded iMVC signals were used to normalize the amplitude of the sEMG signals.
The participant was asked to perform inline skating with roller skates on a motorized treadmill with a belt surface 2.5 m wide and 3.5 m long (RL3500E, Rodby Innovation AB, Vänge, Sweden) at two different speeds, first at 20 km/h and then 32 km/h, with an inclination of 1°. The two trials at two speeds were performed half an hour apart to avoid confounding effects due to muscle fatigue.

2.4. Data Analysis

2.4.1. Skating Cycle Definition

The skating cycle was defined starting from the vertical acceleration ( a v ) and the muscle data (Figure 1). The acceleration peaks were identified. Then, looking at the VL or GMed muscle [15], the propulsion phase was identified as the time in which the muscle was active (from the first to the second peak of a v within a skating cycle) and the recovery phase as the time in which the muscle was deactivated (from the second to the third peak of a v within a skating cycle). We identified nine skating cycles at 20 km/h and nine at 32 km/h. Then, to average the different cycles and compare the different speeds, we time-normalized all the skating cycle acceleration and EMG data, after the pre-processing described below, with a polynomial procedure for the same number of samples (201 samples) [16].

2.4.2. sEMG

The sEMG signals were processed as follows: the iMVC and the sEMG raw data of each trial were band-pass filtered (4th-order Butterworth filter) between 20 and 400 Hz [17,18]; subsequently, a full-wave rectification of the signals was performed and low-pass filtering (4th-order Butterworth filter) at 10 Hz [19,20] was applied to extract the envelope of muscle activity; the rectified and filtered sEMG data related to each skating cycle were expressed as a percentage of the sEMG peak value [21,22,23], calculated as the maximum values detected for each of the iMVCs [21,22,24,25,26].
From the elaborated sEMG signals of each cycle, we computed the maximum value (Max) and the average rectified value (ARV) within the cycle.
Furthermore, we considered the following four muscles groups:
-
RVL, RBF, RTA, and RSOL (group A);
-
LVL, LBF, LTA, and LSOL (group B);
-
RGMax, RRF, RGMed, and RAL (group C);
-
LGMax, LRF, LGMed, and LRAL (group D).
For each group (A, B, C, and D), we calculated the simultaneous activation of the muscles (coactivation) by considering the Rudolph co-activation function for each pair of antagonist muscles [27] as follows:
R C k = s E M G H k + s E M G L k × s E M G L k / s E M G H k
where k is the kth sample of the sEMG signals and s E M G H and s E M G L are the highest and the lowest activity between the antagonist muscle pairs.
Furthermore, we calculated the time-varying multi-muscle co-activation function (TMCf) proposed by Ranavolo and colleagues [28].
T M C f d k , k = 1 1 1 + e 12 d k 0.5 .   ( m = 1 M s E M G m ( k ) / M )   2 m a x m = 1 M [ s E M G m k ]
where d ( k ) is the mean of the differences between the kth samples of each pair of sEMG signals:
d ( k ) = m = 1 M 1 n = m + 1 M | s E M G m k s E M G n ( k ) | J ( M ! / ( 2 ! M 2 ! ) )
In the above equations, J is 200 (the length of the signal); M is the number of considered muscles; and s E M G m k and s E M G n k are the kth sample values of the envelope of the sEMG signals of the mth and nth muscles, respectively.
Then, from each co-activation function, we computed the Max and the ARV within the cycle.

3. Results

Figure 2A shows the mean vertical ( a v ), medio-lateral ( a M L ), and antero-posterior ( a A P ) acceleration curves during the skating cycles at two velocities (20 and 32 km/h). The vertical lines represent the transition event (mean among all cycles) from the propulsion phase to the recovery phase. Figure 2B shows the mean values (±SD) of the a v , a M L , and a A P within the skating cycles and the propulsion and recovery phases at two velocities (20 and 32 km/h).
Figure 3 shows the mean (±SD) muscle curves during the skating cycles at two velocities (20 and 32 km/h). The vertical lines represent the mean (±SD) transition event from the propulsion phase to the recovery phase.
Figure 4 shows the Max and ARV (±SD) for each muscle curve during the skating cycles and the propulsion and recovery phases at two velocities (20 and 32 km/h).
Figure 5 shows the mean (±SD) Rudolph coactivation curves for each pair of muscles and the TMCf coactivation curves for each muscle group, A, B, C and D, during the skating cycles at two velocities (20 and 32 km/h). The vertical lines represent the mean (±SD) transition event from the propulsion phase to the recovery phase.
Figure 6 shows the Max and ARV (±SD) for each Rudolph and TMCf coactivation curve during the skating cycles and the propulsion and recovery phases at two velocities (20 and 32 km/h).

4. Discussion

With this case study, we aimed to investigate the spatial–temporal and muscular behavior of a professional female athlete on a two-speed treadmill.
From a kinematics point of view, the average value of the vertical component of acceleration is increased at higher speeds throughout the entire skating cycle and in the propulsion phase (Figure 2b). This is mainly due to the need, since the athlete is stationary along the antero-posterior direction, to gain speed in the push phase. The increased vertical component of the acceleration is also associated with an increase in the duration of the propulsion phase. This speed-based induced motor mechanism suggests the possibility of training the technical gesture and the reference muscles in targeted re-athleticization or athletic preparation programs.
From an analysis of the results of the muscular behaviors, it can be seen that higher velocities imply higher muscle commitments (Figure 4). In fact, the VL, BF, TA, SOL, GMax, RF, GMed, and AL maximum values increased at 32 km/h in the entire skating cycle and in the propulsion phase. The increase in the peak activation of the hip, knee, and ankle extensor muscles explains the increase in the vertical component of the acceleration.
In terms of the ARV, however, it is possible to observe a significant increase with speed in the VL, BF, SOL, GMed, and AL muscles in the skating cycle and the propulsion phase (Figure 4). This is attributable to the need to manage a wider propulsion phase and a greater push along the vertical component for the entire duration of the propulsion phase itself.
For the TA and AL, then, in terms of both Max and ARV, there is also an increase with speed in the recovery phase, as shown in Figure 4. This is due to the need to recover an adequate posture for the subsequent propulsion phase.
In general, both the coactivation calculated with Rudolph’s approach and TMCf show highest values at 32 km/h, both in terms of the Max and ARV in the skating cycle and in both the propulsion and recovery subphases (Figure 6). This is in line with what has also been reported in other studies on locomotor tasks such as walking and running [29,30,31].
These results suggest that the contribution to = limb stiffening during skating is mostly due to the muscle co-activation of the extensors according to their function in load acceptance and their propulsive role [32]. This of also interest because the flexor muscles play a key role in the transition from the propulsive to the recovery phase.
The only exception is found in the Max of the Rudolph coactivation for the GMax-RF pair and for the Max of the TMCf for the GMax-RF-GMed-AL, which shows a slight reduction in the recovery phase at the highest speed (Figure 6).
In addition, from Figure 4, a consistent symmetry between the left and right sides can be observed in general, excluding VL, with RF showing much higher values on the left side than on the right side; TA, SOL, GMax, and GMed show slightly higher values on the left than on the right, both in the full cycle and in the propulsion and recovery phases. This asymmetry could be due to the fact that the athlete is right-handed and needs to activate the muscle of the non-dominant side more. From Figure 6, on the other hand, greater symmetry emerges between the left and right sides in the coactivation parameters (Max and ARV), both in the whole skating cycle and in each of the two subphases. These results confirm the symmetrical nature of the motor task on the treadmill, unlike what happens on the road where, in curvilinear sections, there can be an asymmetrization between the two sides [33]. In skating, training should be designed to minimize the risk of muscle fatigue asymmetry and to decrease asymmetry [34]. In this regard, the literature has provided a functional protocol of analysis on roads, which, through surface electromyographic instrumentation, allows for the monitoring of both kinematics and muscle activation of the investigated districts in a professional athlete. This study incorporates the same acquisition methods and instrumentation already used on the skating performance of a former world champion athlete, serving as a performance model [15,35].
The results of this study must be considered absolutely preliminary, as they can be attributed to a case study. On the other hand, the differences induced by the two speeds set on the treadmill suggest the need to investigate a larger sample in order to analyze any differences in gender (we have analyzed only a female), age, right- and left-handed people, and the experience of the athlete.

5. Conclusions

Performing the skating task on a treadmill at different speeds can be particularly useful for inducing different motor behaviors, with the aim of training different functions. Furthermore, the treadmill allows for the careful evaluation of the technical gestures, also due to the greater simplicity in carrying out instrumental measurements with wearable sensors.

Author Contributions

Conceptualization, G.B. and L.M.; methodology, T.V., G.C. and A.R.; software, G.S. and L.M.; validation, F.D.M. and H.B.; formal analysis, T.V., G.C. and A.R.; investigation, L.B. and B.P.; resources, T.V., G.C., and A.R.; data curation, B.P. and L.B.; writing—original draft preparation, T.V., G.C. and A.R.; writing—review and editing, G.B., G.S., F.D.M., H.B., T.V., G.C., A.R., B.P., L.B. and L.M.; visualization, G.S.; supervision, L.B. and B.P.; project administration, G.B. and L.M.; funding acquisition, G.B. and L.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

This study was conducted in accordance with the Declaration of Helsinki; the approval of the Institutional Review Board was not applicable for a single case study not involving patients or animals.

Informed Consent Statement

Written informed consent has been obtained from the subjects to publish this paper.

Data Availability Statement

The dataset is available on request from the authors.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Irshad, K.; Feldman, L.S.; Lavoie, C.; Lacroix, V.I.; Mulder, D.S.; Brown, R.A. Operative management of “hockey groin syndrome”: 12 years of experience in National Hockey League players. Surgery 2001, 130, 759–764. [Google Scholar] [CrossRef] [PubMed]
  2. Coetzee, D.; Coetzee, F.F.; Schall, R.; Sinclair, C. Gluteal muscle activation during rehabilitation exercises in female field hockey players”. S. Afr. J. Physiother. 2021, 77, 1578. [Google Scholar] [CrossRef] [PubMed]
  3. Emery, C.A.; Meeuwisse, W.H. Risk factors for groin injuries in hockey. Med. Sci. Sports Exerc. 2001, 33, 1423–1433. [Google Scholar] [CrossRef] [PubMed]
  4. Emery, C.A.; Meeuwisse, W.H.; Powell, J.W. Groin and abdominal strain injuries in the National Hockey League. Clin. J. Sport Med. 1999, 9, 151–156. [Google Scholar] [CrossRef]
  5. Buckeridge, E.; Levangie, M.C.; Stetter, B.; Nigg, S.R.; Nigg, B.M. An on-ice measurement approach to analyse the biomechanics of ice hockey skating. PLoS ONE 2015, 10, e0127324. [Google Scholar] [CrossRef]
  6. De Boer, R.W.; Cabri, J.; Vaes, W.; Clarijs, J.P.; Hollander, A.P.; De Groot, G.; Van Ingen Schenau, G.J. Moments of force, power, and muscle coordination in speed-skating. Int. J. Sports Med. 1987, 8, 371–378. [Google Scholar] [CrossRef]
  7. Goudreault, R. Forward Skating in Ice Hockey: Comparison of EMG Activation Patterns of [Sic] at Three Velocities Using a Skate Treadmill. Master’s Thesis, McGill University, Montréal, QC, Canada, 2002. [Google Scholar]
  8. Encarnación-Martínez, A.; Pérez-Soriano, P.; Sanchis-Sanchis, R.; García-Gallart, A.; Berenguer-Vidal, R. Validity and Reliability of an Instrumented Treadmill with an Accelerometry System for Assessment of Spatio-Temporal Parameters and Impact Transmission. Sensors 2021, 21, 1758. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  9. Abbasi, A.; Yazdanbakhsh, F.; Tazji, M.K.; Aghaie Ataabadi, P.; Svoboda, Z.; Nazarpour, K.; Vieira, M.F. A comparison of coordination and its variability in lower extremity segments during treadmill and overground running at different speeds. Gait Posture 2020, 79, 139–144. [Google Scholar] [CrossRef] [PubMed]
  10. Marino, G.W. Selected mechanical factors associated with acceleration in ice skating. Res. Q. Exerc. Sport 1983, 54, 234–238. [Google Scholar] [CrossRef]
  11. Tyler, T.F.; Nicholas, S.J.; Campbell, R.J.; Donellan, S.; Mchugh, M.P. The effectiveness of a preseason exercise program to prevent adductor muscle strains in professional ice hockey players. Am. J. Sports Med. 2002, 30, 680–683. [Google Scholar] [CrossRef]
  12. Turcotte, R.A.; Pearsall, D.J.; Montgomery, D.L.; Lefebvre, R.; Ofir, D.; Loh, J.J. Comparison of Ice versus Treadmill Skating—Plantar Force Distribution Patterns. ASTM Spec. Tech. Publ. 2004, 1446, 265–271. [Google Scholar] [CrossRef]
  13. Hermens, H.J.; Freriks, B.; Disselhorst-Klug, C.; Rau, G. Development of recommendations for SEMG sensors and sensor placement procedures. J. Electromyogr. Kinesiol. 2000, 10, 361–374. [Google Scholar] [CrossRef] [PubMed]
  14. Kaartinen, S.; Venojärvi, M.; Lesch, K.; Tikkanen, H.; Vartiainen, P.; Stenroth, L. Lower limb muscle activation patterns in ice-hockey skating and associations with skating speed. Sports Biomech. 2021, 1–16. [Google Scholar] [CrossRef]
  15. Bongiorno, G.; Biancuzzi, H.; Dal Mas, F.; Fasano, G.; Miceli, L. Roller Speed Skating Kinematics and Electromyographic Analysis: A Methodological Approach. Sports 2022, 10, 209. [Google Scholar] [CrossRef] [PubMed]
  16. Serrao, M.; Rinaldi, M.; Ranavolo, A.; Lacquaniti, F.; Martino, G.; Leonardi, L.; Conte, C.; Varrecchia, T.; Draicchio, F.; Coppola, G.; et al. Gait Patterns in Patients with Hereditary Spastic Paraparesis. PLoS ONE 2016, 11, e0164623. [Google Scholar] [CrossRef]
  17. Butler, H.L.; Newell, R.; Hubley-Kozey, C.L.; Kozey, J.W. The Interpretation of AbdominalWall Muscle Recruitment Strategies Change When the Electrocardiogram (ECG) Is Removed from the Electromyogram (EMG). J. Electromyogr. Kinesiol. 2009, 19, e102–e113. [Google Scholar] [CrossRef]
  18. Drake, J.D.M.; Callaghan, J.P. Elimination of Electrocardiogram Contamination from Electromyogram Signals: An Evaluation of Currently Used Removal Techniques. J. Electromyogr. Kinesiol. 2006, 16, 175–187. [Google Scholar] [CrossRef]
  19. Rinaldi, M.; D’Anna, C.; Schmid, M.; Conforto, S. Assessing the influence of SNR and pre-processing filter bandwidth on the extraction of different muscle co-activation indexes from surface EMG data. J. Electromyogr. Kinesiol. 2018, 43, 184–192. [Google Scholar] [CrossRef]
  20. Winter, D.A. Biomechanics and Motor Control of Human Movement, 4th ed.; John Wiley & Sons, Inc.: Hoboken, NJ, USA; University of Waterloo: Waterloo, ON, Canada, 2009. [Google Scholar]
  21. Hermens, H.J.; Freriks, B.; Merletti, R.; Stegeman, D.; Blok, J.; Rau, G.; Disselhorst-Klug, C.; Hagg, G. European recommendations for surface electromyography. Roessingh Res. Dev. 1999, 8, 13–54. [Google Scholar]
  22. Burden, A. How should we normalize electromyograms obtained from healthy participants? What we have learned from over 25 years of research. J. Electromyogr. Kinesiol. 2010, 20, 1023–1035. [Google Scholar] [CrossRef]
  23. Staudenmann, D.; Roeleveld, K.; Stegeman, D.F.; van Dieën, J.H. Methodological aspects of SEMG recordings for force estimation–a tutorial and review. J. Electromyogr. Kinesiol. 2010, 20, 375–387. [Google Scholar] [CrossRef] [PubMed]
  24. Ball, N.; Scurr, J. An assessment of the reliability and normalization of tests used to elicit reference muscular actions for electromyographical normalization. J. Electromyogr. Kinesiol. 2010, 20, 81–88. [Google Scholar] [CrossRef] [PubMed]
  25. Marras, W.S.; Davis, K.G. A non-MVC EMG normalization technique for the trunk musculature: Part 1. Method development. J. Electromyogr. Kinesiol. 2001, 11, 1–9. [Google Scholar] [CrossRef] [PubMed]
  26. Marras, W.S.; Davis, K.G.; Maronitis, A.B. A non-MVC EMG normalization technique for the trunk musculature: Part 2. Validation and use to predict spinal loads. J. Electromyogr. Kinesiol. 2001, 11, 11–18. [Google Scholar] [CrossRef]
  27. Rudolph, K.S.; Axe, M.J.; Snyder-Mackler, L. Dynamic stability after ACL injury: Who can hop? Knee Surg. Sports Traumatol. Arthrosc. 2000, 8, 262–269. [Google Scholar] [CrossRef]
  28. Ranavolo, A.; Mari, S.; Conte, C.; Serrao, M.; Silvetti, A.; Iavicoli, S.; Draicchio, F. A new muscle co-activation index for biomechanical load evaluation in work activities. Ergonomics 2015, 58, 966–979. [Google Scholar] [CrossRef]
  29. Fiori, L.; Castiglia, S.F.; Chini, G.; Draicchio, F.; Sacco, F.; Serrao, M.; Tatarelli, A.; Varrecchia, T.; Ranavolo, A. The Lower Limb Muscle Co-Activation Map during Human Locomotion: From Slow Walking to Running. Bioengineering 2024, 11, 288. [Google Scholar] [CrossRef]
  30. Ivanenko, Y.P.; Poppele, R.E.; Lacquaniti, F. Spinal Cord Maps of Spatiotemporal Alpha-Motoneuron Activation in Humans Walking at Different Speeds. J. Neurophysiol. 2006, 95, 602–618. [Google Scholar] [CrossRef]
  31. Dewolf, A.H.; Ivanenko, Y.P.; Zelik, K.E.; Lacquaniti, F.; Willems, P.A. Differential Activation of Lumbar and Sacral Motor Pools during Walking at Different Speeds and Slopes. J. Neurophysiol. 2019, 122, 872–887. [Google Scholar] [CrossRef]
  32. Møller, M.; Sinkjaer, T.; Duysens, J. Contributions to the Understanding of Gait Control; University of Copenhagen: Copenhagen, Denmark, 2014. [Google Scholar]
  33. Konieczny, M.; Skorupska, E.; Domaszewski, P.; Pakosz, P.; Skulska, M.; Herrero, P. Relationship between latent trigger points, lower limb asymmetry and muscle fatigue in elite short-track athletes. BMC Sports Sci. Med. Rehabil. 2023, 15, 109. [Google Scholar] [CrossRef]
  34. Konieczny, M.; Pakosz, P.; Witkowski, M. Asymmetrical fatiguing of the gluteus maximus muscles in the elite short-track female skaters. BMC Sports Sci. Med. Rehabil. 2020, 12, 48. [Google Scholar] [CrossRef] [PubMed]
  35. Bongiorno, G.; Sisti, G.; Dal Mas, F.; Biancuzzi, H.; Bortolan, L.; Paolatto, I.; Rosa, M.; Miceli, L. Surface electromyographic wheel speed skate protocol and its potential in athletes’ performance analysis and injury prevention. J. Sports Med. Phys. Fitness 2023, 63, 1093–1099. [Google Scholar] [CrossRef] [PubMed]
Figure 1. An example of skating cycles, propulsion, and recovery phase definitions, considering the vertical acceleration and the muscle data. RVL: right vastus lateralis.
Figure 1. An example of skating cycles, propulsion, and recovery phase definitions, considering the vertical acceleration and the muscle data. RVL: right vastus lateralis.
Sensors 24 05738 g001
Figure 2. The mean vertical ( a v ), medio-lateral ( a M L ), and antero-posterior ( a A P ) acceleration curves (A) during the skating cycles at two velocities (20 and 32 km/h) and the mean values (±SD) of the a v , a M L , and a A P accelerations (B) within the skating cycles and the propulsion and recovery phases at two velocities.
Figure 2. The mean vertical ( a v ), medio-lateral ( a M L ), and antero-posterior ( a A P ) acceleration curves (A) during the skating cycles at two velocities (20 and 32 km/h) and the mean values (±SD) of the a v , a M L , and a A P accelerations (B) within the skating cycles and the propulsion and recovery phases at two velocities.
Sensors 24 05738 g002
Figure 3. The mean (±SD) muscles curves during the skating cycles at two velocities (20 and 32 km/h). The vertical lines represent the mean (±SD) transition event from the propulsion phase to the recovery phase. SOL: soleus; GMax: gluteus maximus; GMed: gluteus medius; AL: adductor longus; RF: rectus femoris; BF: biceps femoris; VL: vastus lateralis; TA: tibialis anterior.
Figure 3. The mean (±SD) muscles curves during the skating cycles at two velocities (20 and 32 km/h). The vertical lines represent the mean (±SD) transition event from the propulsion phase to the recovery phase. SOL: soleus; GMax: gluteus maximus; GMed: gluteus medius; AL: adductor longus; RF: rectus femoris; BF: biceps femoris; VL: vastus lateralis; TA: tibialis anterior.
Sensors 24 05738 g003
Figure 4. Maximum value (Max) and average rectified value (ARV) within the cycle. (±SD) for each muscle curve during the skating cycles and the propulsion and recovery phases at two velocities (20 and 32 km/h). SOL: soleus; GMax: gluteus maximus; GMed: gluteus medius; AL: adductor longus; RF: rectus femoris; BF: biceps femoris; VL: vastus lateralis; TA: tibialis anterior.
Figure 4. Maximum value (Max) and average rectified value (ARV) within the cycle. (±SD) for each muscle curve during the skating cycles and the propulsion and recovery phases at two velocities (20 and 32 km/h). SOL: soleus; GMax: gluteus maximus; GMed: gluteus medius; AL: adductor longus; RF: rectus femoris; BF: biceps femoris; VL: vastus lateralis; TA: tibialis anterior.
Sensors 24 05738 g004
Figure 5. Mean (±SD) Rudolph and TMCf coactivation curves during the averaged skating cycle at two velocities (20 and 32 km/h). The vertical lines represent the mean (±SD) transition event from the propulsion phase to the recovery phase. SOL: soleus; GMax: gluteus maximus; GMed: gluteus medius; AL: adductor longus; RF: rectus femoris; BF: biceps femoris; VL: vastus lateralis; TA: tibialis anterior.
Figure 5. Mean (±SD) Rudolph and TMCf coactivation curves during the averaged skating cycle at two velocities (20 and 32 km/h). The vertical lines represent the mean (±SD) transition event from the propulsion phase to the recovery phase. SOL: soleus; GMax: gluteus maximus; GMed: gluteus medius; AL: adductor longus; RF: rectus femoris; BF: biceps femoris; VL: vastus lateralis; TA: tibialis anterior.
Sensors 24 05738 g005
Figure 6. Maximum value (Max) and average rectified value (ARV) within the cycle (±SD) for each muscle curve during the skating cycles and the propulsion and recovery phases at two velocities (20 and 32 km/h). SOL: soleus; GMax: gluteus maximus; GMed: gluteus medius; AL: adductor longus; RF: rectus femoris; BF: biceps femoris; VL: vastus lateralis; TA: tibialis anterior.
Figure 6. Maximum value (Max) and average rectified value (ARV) within the cycle (±SD) for each muscle curve during the skating cycles and the propulsion and recovery phases at two velocities (20 and 32 km/h). SOL: soleus; GMax: gluteus maximus; GMed: gluteus medius; AL: adductor longus; RF: rectus femoris; BF: biceps femoris; VL: vastus lateralis; TA: tibialis anterior.
Sensors 24 05738 g006
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Bongiorno, G.; Sisti, G.; Dal Mas, F.; Biancuzzi, H.; Varrecchia, T.; Chini, G.; Ranavolo, A.; Pellegrini, B.; Bortolan, L.; Miceli, L. The Kinematic and Electromyographic Analysis of Roller Skating at Different Speeds on a Treadmill: A Case Study. Sensors 2024, 24, 5738. https://doi.org/10.3390/s24175738

AMA Style

Bongiorno G, Sisti G, Dal Mas F, Biancuzzi H, Varrecchia T, Chini G, Ranavolo A, Pellegrini B, Bortolan L, Miceli L. The Kinematic and Electromyographic Analysis of Roller Skating at Different Speeds on a Treadmill: A Case Study. Sensors. 2024; 24(17):5738. https://doi.org/10.3390/s24175738

Chicago/Turabian Style

Bongiorno, Giulia, Giulio Sisti, Francesca Dal Mas, Helena Biancuzzi, Tiwana Varrecchia, Giorgia Chini, Alberto Ranavolo, Barbara Pellegrini, Lorenzo Bortolan, and Luca Miceli. 2024. "The Kinematic and Electromyographic Analysis of Roller Skating at Different Speeds on a Treadmill: A Case Study" Sensors 24, no. 17: 5738. https://doi.org/10.3390/s24175738

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Article metric data becomes available approximately 24 hours after publication online.
Back to TopTop