Next Article in Journal
Unsupervised Transfer Learning Method via Cycle-Flow Adversarial Networks for Transient Fault Detection under Various Operation Conditions
Next Article in Special Issue
Advanced Necklace for Real-Time PPG Monitoring in Drivers
Previous Article in Journal
Antenna Integration for Millimeter-Wave RF Sensing and Millimeter-Wave Communication Mountable on a Platform
Previous Article in Special Issue
Improving Eye-Tracking Data Quality: A Framework for Reproducible Evaluation of Detection Algorithms
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Characterization of Great Toe Extension Strength Using ToeScale—A Novel Portable Device

by
Raghuveer Chandrashekhar
1,
Luciana Fonseca Perez
2 and
Hongwu Wang
1,*
1
Department of Occupational Therapy, College of Public Health and Health Professions, University of Florida, Gainesville, FL 32611, USA
2
John Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL 32611, USA
*
Author to whom correspondence should be addressed.
Sensors 2024, 24(15), 4841; https://doi.org/10.3390/s24154841
Submission received: 9 June 2024 / Revised: 17 July 2024 / Accepted: 22 July 2024 / Published: 25 July 2024

Abstract

:
Great toe strength (GTS) weakness is linked to declines in balance and mobility. Accurately assessing GTS, particularly great toe extension strength (GTES), is often neglected in clinical evaluations due to cumbersome and subjective methods. This study aims to characterize the force development curve output from the ToeScale and examine GTES variations with age, sex, BMI, and grip strength (GS) using traditional analyses and machine learning (ML). We conducted a pilot, cross-sectional feasibility study with convenience samples. We assessed GS using a hand-grip dynamometer and GTES using the ToeScale. The data analysis included descriptive statistics, correlations, independent samples t-tests, and accuracy and area under the curve (AUC) scores for three ML models. Thirty-one participants (males: 9; females: 22), 14 young (18–24 years) and 17 older (>65 years) adults, participated in the study. Males had significantly higher peak GTES than females in both age groups. The associations of GTES parameters with BMI and GS varied by age and sex. The ML model accuracies and AUC scores were low–moderate but aligned with traditional analyses. Future studies with larger samples and optimized ML models are needed.

1. Introduction

The strength and range of motion of the great toe/first metatarsophalangeal joint (1st-MTJ) are critical for normal walking and balance [1,2,3,4]. The great toe flexors and extensors play a significant role in sensation/proprioception, generating propulsive forces, weight bearing, foot clearance, and supporting the foot arch during different phases of gait and other functional activities [5,6,7,8,9]. Reduced muscle strength, limited range of motion, and/or loss of sensation in the great toe can affect an individual’s balance and their ability to walk and perform activities of daily living (ADLs), and reduce participation in community activities, resulting in a reduction in the individual’s quality of life (QoL) [10,11,12,13,14,15,16,17]. Furthermore, various pathological conditions (neurological and non-neurological), such as peripheral neuropathy, radiculopathy, Charcot–Marie–Tooth disease, and hallux/toe deformities, have also been associated with the atrophy and/or reduction in the strength of great toe muscles [18,19,20,21,22,23,24]. Multiple studies have also reported an association of great toe strength (GTS) with age and sex, making it a potential clinical biomarker that could be used to detect or evaluate the onset and progression of different health conditions [7,25,26,27,28,29].
Despite its critical biomechanical and functional roles, GTS, particularly great toe extension strength (GTES), is often overlooked during routine clinical practice due to the lack of a reliable and robust tool for GTES measurement and the subjective nature of existing methods [30,31,32,33]. To address the limitations of existing GTS measurement methods and devices and the clinical need for their improvement, we recently developed the ToeScale, a novel, portable device [34,35]. A preliminary study using the ToeScale and comparing it with the results from a manual muscle test (MMT) indicates an association between the values obtained by both methods, and the ToeScale shows stronger discriminative ability than the MMT [35]. In addition, the ToeScale output has a force development curve over time, showing not just a peak force that can be measured using a hand-held dynamometer, but also information on how the force was developed over time. However, the characterization of this ToeScale output curve for clinical use is yet to be further examined.
Thus, the primary aim of this study is to characterize the output force development curve of the ToeScale by manually hand-picking features from the force development curve based on its relevance to the muscle’s physiological performance and assess how the different GTES parameters related to demographic variables such as age and sex and grip strength. The secondary objective is to explore the feasibility of employing machine learning (ML) methods to characterize ToeScale output curves by age and sex based on the time series data of the force development curve.

2. Materials and Methods

2.1. Study Design, Inclusion Criteria, and Measurement Protocol

In this cross-sectional study, data were collected from a convenience sample of younger (aged between 18 and 24 years) and older adults (>60 years of age). As this study focuses on the preliminary characterization and analysis of GTES as well as the feasibility of using the ToeScale in a community setting, we did not have any exclusion criteria for the participants. All participants completed a demographic and physical activity questionnaire and a grip strength assessment using a Jamar handgrip dynamometer (Performance Health Supply Inc., Warrenville, IL, USA) [36]. Finally, the great toe extension strength (GTES) was assessed using the ToeScale [34,35], a novel, portable device. GTES was measured with the participants seated with their knee and ankle at 90° as shown in Figure 1 below. In this seated position, the participants were instructed to raise their great toe, i.e., extend it against the toe cap of the ToeScale, as hard as possible and try to aim for a higher force for 10 s continuously. We selected a 10-s duration for the trials based on our previous work [35]. The measurement of GTES using the ToeScale is shown in Figure 1.

2.2. Great Toe Extension Strength Characterization and Classification

The device recorded the force in kilograms with a sampling frequency of 50 Hz, resulting in a force–time curve with 500 data points for each participant, with one column representing time and the second column representing GTES in Kg, and the data were saved as a text file. For the first objective, the force–time curve was characterized using MATLAB. The different parameters/features of the GTES curve extracted included peak force; time to 80% of the peak, i.e., rise time; average force after reaching the 80% of the peak force; percentage of data points in each trial equal to or above the average value; and the RFD (80% peak force divided by the rise time). The different GTES parameters extracted from the GTES curve are shown in Figure 1 below. These parameters were then compared across age groups/sexes. This study chose 80% of the peak force as the cut-off to calculate rise time. The literature reports that all muscle/muscle group motor units are recruited at 80% of the maximum voluntary contraction, emphasizing its significance [37]. Using 80% of the peak force as the cut-off would also help standardize the rise time calculation. The other clinically meaningful measure of GTES is RFD, which has been associated with postural stability and could be a potential biomarker for acute muscle damage and exercise-induced fatigue [38]. RFD in this study is defined as the rate of rise in toe strength per unit time (Ns-1) to reach 80% of the peak toe strength.
For the second objective, the Python 3.0 [39] programming language was used to apply machine learning (ML) algorithms to classify the GTES force–time curves based on age and sex. The units of all force data, i.e., GS and GTES force–time curves, were converted to newtons before the analyses. As this is a preliminary analysis, only supervised ML models [40,41,42] were applied to the GTES force–time curves using age and sex as the two target variables for classification. We applied k-nearest neighbors (k-NN), support vector machine (SVM), and random forest (RF), as these methods are frequently used models due to their unique advantages for smaller time-series datasets [41]. The k-NN classifier is advantageous with small datasets due to its simplicity and effectiveness with limited data [43,44,45], the RF classifier is more robust with handling overfitting and effective in handling feature importance [46], and lastly, the SVM classifier is also robust with handling overfitting and non-linear relationships [42,47]. Before running any of the ML models, the GTES data with missing data were imputed based on the time-point within the 10 s trial where the data were missing. The only missing data observed in the GTES trials were those which had <10 missing data points at the end of the 10 s trial, which were imputed with the last available value to ensure that all datasets had an equal number of data points. Once the data were cleaned and imputed, the ML models were applied directly to the raw dataset (500 data points), without using the manually extracted features in the traditional analyses, to assess the feasibility of using ML as a method to classify the given GTES force–time curves based on the demographic variables of age (2 classes: old/young) and sex (2 classes: male/female).

2.3. Data Analysis Plan

The descriptives were calculated for all variables, including the different parameters of the GTES force–time curve. ANOVAs, independent sample t-tests, and correlation analyses were conducted to assess and compare the relationships of the different GTES parameters with GS and demographics such as age, sex, and body mass index (BMI). In the machine learning approach, different supervised ML models (all datasets were labeled for both the target variables) were applied to the GTES force–time curves, and the models’ accuracy and area under the receiver operating characteristic curve (AUC) were calculated and compared. For the ML model analyses, we also used the standard training (single train–test split) as well as cross-validation (3-fold and 5-fold) training approaches.

3. Results

3.1. Demographics

Thirty-one participants completed the study, and their demographics are presented below in Table 1.

3.2. Traditional Analyses

Table 2 below summarizes the different GTES parameters and the GS. The peak GTES, average GTES, and rate of force development (RFD) were lower and the rise time to 80% of the peak was longer among older adults than younger adults. While there was no statistical significance in the difference in any GTES parameters except rise time between older and younger adults, there was a clinically meaningful difference of over 8 N in the peak GTES and over 10 N/s in the RFD. The independent samples t-test showed that all the differences in GTES parameters between males and females were statistically significant, with a difference of >13 N in peak GTES, >14 N/s in RFD, and >1.5 s rise time. Males had a higher peak GTES and RFD and a quicker rise time than females. A two-way ANOVA of the GTES parameters showed a lack of significance in the interaction effect of age and sex. However, Table 2 shows that older females have the lowest peak GTES and RFD and the longest rise time, which warrants further investigation.
The correlation analysis results in Table 3 below show that peak GTES correlates more strongly with BMI than GS, especially among older adults (r = 0.594). A significant (p < 0.05) moderate positive correlation for the total sample (r = 0.545), older adults (r = 0.519), and younger adults (r = 0.546) was observed in the correlation between peak GTES and GS.

3.3. Machine Learning Analyses

The first step in applying ML to characterize the GTES curve was to check whether machine learning classifiers can support the evidence from the traditional analyses by accurately differentiating between age and sex. The accuracy of all three classifiers was the same (66.67%) when age was the target variable. With sex as the target variable, the SVM classifier had the highest accuracy of 66.67%, while the k-NN (five nearest neighbors) and RF classifiers had an accuracy of 55.56% each. By further varying the hyperparameters, such as kernel type, number of nearest neighbors, etc., the k-NN (10 nearest neighbors) classifier had the highest accuracy of 77.78% when sex was the target variable. The accuracy scores and the AUC values for the different models are presented in Table 4 below. The AUC represents the true positive-to-false positive rates in the classification, and values of 0.5 or less indicate a lack of ability of the ML model to distinguish between the classes and is equivalent to random guessing [48].

4. Discussion

In this study, we characterized the ToeScale output curve by applying traditional methods based on key features for muscle performance and explored the feasibility of applying ML methods to classify the time series data. To our knowledge, this is the first study to quantify great toe strength beyond just peak force. The key parameters extracted from the GTES force development curve included the peak GTES, average GTES, rise time, and RFD. The results showed statistically significant differences in all GTES parameters between males and females, and the statistically significant differences observed while comparing the GTES parameters by age were in the rise time and RFD. The differences in the peak and average GTES between older and younger adults observed in this study were 7 N and 8 N, respectively, and this is supported by many studies reporting similar trends and differences in great toe strength (GTS) among healthy older and younger adults [28,31]. Existing studies [49,50] also support sex-based differences (~7–8 N), and in this study, males had a higher peak and average GTES than females by 16 N and 10 N, respectively. Another important component of muscle strength that is often overlooked is RFD. Due to its clinical and physiological significance, there has been an increase in the number of studies reporting RFD and its association with muscle function and performance [38,51,52,53,54]. Among the studies reporting the RFD, very few specifically report the RFD of the great toe muscles. Kamasaki et al., 2024 and Sarikaya et al., 2022 [55,56] reported a strong association of RFD in the great toe with better functional mobility and balance outcomes. Additionally, Kamasaki et al., 2024 [55] reported a higher RFD among younger adults compared to older adults, which is consistent with the findings of this study, where the RFD was ~15 N/s higher among younger adults. Although Kamaski et al. did not report any sex-based differences, our study showed that males had 21 N/s higher RFD than females [56]. Finally, our study revealed that older adults had a longer rise time than younger adults. While none of the existing studies report results on rise time, the prolonged rise time in older adults is expected, as muscle responses have been reported to slow down due to aging [57]. This study shows a decline in all GTES parameters with age (Table 1), consistent with studies reporting the effects of age on muscle strength [28,31,55].
The correlation analyses summarized in Table 2 revealed moderate levels of association between the different GTES parameters and BMI, which varied by age, and a low-to-moderate correlation between GS and BMI across all age groups. Among all the GTES parameters, peak GTES had the highest correlation with BMI, particularly among older adults (r = 0.594, p = 0.012). The rise time of the RFD was statistically significantly correlated with BMI. The analyses between the different GTES parameters with GS show that all GTES parameters were statistically significantly correlated with GS with moderate levels of association (Table 2). However, when evaluated separately, while the peak GTES was statistically significantly correlated with GS in both younger (r = 0.546, p = 0.043) and older adults (r = 0.519, p = 0.033), the average GTES (r = 0.516, p = 0.034) and RFD (r = 0.473, p = 0.055) were more strongly correlated with GS among older adults when compared to younger adults. While BMI and GS are well-established measures commonly used as biomarkers of physical health and mobility and overall muscle strength status [58,59,60], they are known for their low sensitivity to changes in mobility when compared to measures of lower-extremity functions or muscle strength [57]. Studies have reported foot or great toe strength measures to be better predictors of physical health and mobility as they are directly involved in walking [61,62]. The moderate correlations between GTES parameters, especially the peak forces between BMI and GS, highlighted the potential of GTES as a clinical marker for health and functional assessment. The age-based differences in correlations between GTES and BMI and between GTES and GS suggested that changes in BMI and GS are different from changes in GTES with aging.
The three different ML models used to classify the GTES force development curves had moderate accuracies ranging between 55 and 78%, with all models having an accuracy of 66.67% when age was used as the target variable. When sex was used as the target variable, while the SVM had an accuracy of 66.67%, the RF and k-NN (k = 5) models had the lowest accuracy of 55.56%. The model with the highest accuracy was the k-NN classifier with k = 10 with sex as the target variable, which had an accuracy of 77.78%. However, the AUC of this model was 0.36, making this model less reliable for sex-based classification despite the high accuracy. While these models aligned with the results of the traditional analyses, the low AUC scores, particularly for sex-based classification, indicated less effectiveness of the machine learning models in distinguishing between the classes (male/female). The low–moderate AUC values could be attributed to the relatively small sample size and imbalance between males and females [63]. All ML classifiers using age as the target variable had higher AUC scores (0.5–0.75) when compared to ML classifiers using sex as the target variable (0.1–0.5), which further confirmed the impact of the imbalance in sex distribution. Despite the low–moderate AUC scores, these results are promising, and the logical next step in the ML analyses would involve using the manually extracted GTES parameters as “features” to classify by age or sex and compare the accuracy and AUC scores with the results reported in this study.
The current study has several limitations. Firstly, this study has a small sample size, and there is an uneven distribution of males and females included in the study. In addition, we collected only a single trial of GTES and GS measurements, resulting in a smaller dataset for the machine learning methods. The similar values of ML model accuracies and AUC scores across the different models, with and without cross-validation, are indicative of the small and imbalanced dataset analyzed in this study. Secondly, while the results of this study are comparable to the trends in great toe strength reported in existing studies, the extension strength results were difficult to compare with the literature, as most existing studies looking at age- and sex-based differences primarily report on great toe flexion strength.

5. Conclusions

The results of this pilot study are promising, as the differences in the GTES parameters are consistent with the current evidence on the age- and sex-based differences in great toe strength and provide more information than just the peak strength and rate of force development. Peak GTES is more strongly correlated with BMI than GS is with BMI. Thus, these findings indicate that different GTES parameters could potentially provide insights, other than GS and BMI, into different physical health- and mobility-related outcomes and how they are affected by aging and other health conditions. Additionally, the ML classifiers with moderate accuracies and low-to-moderate AUC scores are consistent with the results of the traditional analyses. However, future studies with a larger sample size, more methodological rigor, and measurements of both the flexion and extension strength of the great toe with balance and functional mobility measures are warranted to better understand the impact of GTS on mobility and balance.

Author Contributions

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

Funding

This research received no external funding, and it was all funded by the Technology for Occupational Performance (TOP) Lab at the University of Florida.

Institutional Review Board Statement

Ethical review and approval were waived for this study as the data were collected during a device demonstration at different workshops conducted within the community.

Informed Consent Statement

Patient consent was waived because this study did not involve collecting any of the names or even the exact ages of the participants. None of the patients’ identifiable information was obtained for this study.

Data Availability Statement

The data presented in this study may be requested from the authors. For deidentified human participant data, contact the corresponding author (H.W.). Institutional approvals and data use agreements may be required. The deidentified data are not yet publicly available because the study is ongoing.

Acknowledgments

We would like to thank the residents and staff at Oak Hammock at the University of Florida for their time and for allowing us to conduct our workshop. We would also like to thank the undergraduate research assistants from the Active Learning Program (ALP) course offered at the University of Florida. We would also like to thank the Department of Occupational Therapy for the resources and support.

Conflicts of Interest

H.W. is an inventor on The University of Oklahoma Health Sciences Center patent for the ToeScale used in this work, and R.C. will receive royalties from any future commercialization of the device. The funders had no role in the design of the study; in the collection, analyses, or interpretation of the data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Mann, R.A.; Hagy, J.L. The function of the toes in walking, jogging and running. Clin. Orthop. Relat. Res. 1979, 142, 24–29. [Google Scholar] [CrossRef]
  2. Fujita, M. Role of the metatarsophalangeal (MTP) joints of the foot in level walking. Nihon Seikeigeka Gakkai Zasshi 1985, 59, 985–997. [Google Scholar] [PubMed]
  3. Miyazaki, M. Role and Movement of the Toes During Walking. Nihon Seikeigeka Gakkai Zasshi 1993, 67, 606–616. [Google Scholar] [PubMed]
  4. Fanous, J.; Rice, C. How Important is the Big Toe?: Functional Anatomy of Hallux Flexion. The FASEB Journal 2021, 35. [Google Scholar] [CrossRef]
  5. Nawoczenski, D.A.; Baumhauer, J.F.; Umberger, B.R. Relationship Between Clinical Measurements and Motion of the First Metatarsophalangeal Joint During Gait*. J. Bone Jt. Surg. 1999, 81, 370–376. [Google Scholar] [CrossRef] [PubMed]
  6. Hall, A.L.; Peterson, C.L.; Kautz, S.A.; Neptune, R.R. Relationships between muscle contributions to walking subtasks and functional walking status in persons with post-stroke hemiparesis. Clin. Biomech. 2011, 26, 509–515. [Google Scholar] [CrossRef] [PubMed]
  7. Goldmann, J.-P.; Brüggemann, G.-P. The potential of human toe flexor muscles to produce force. J. Anat. 2012, 221, 187–194. [Google Scholar] [CrossRef]
  8. Goldmann, J.-P.; Sanno, M.; Willwacher, S.; Heinrich, K.; Brüggemann, G.-P. The potential of toe flexor muscles to enhance performance. J. Sports Sci. 2013, 31, 424–433. [Google Scholar] [CrossRef] [PubMed]
  9. Yamauchi, J.; Koyama, K. Force-generating capacity of the toe flexor muscles and dynamic function of the foot arch in upright standing. J. Anat. 2019, 234, 515–522. [Google Scholar] [CrossRef]
  10. Mickle, K.J.; Munro, B.J.; Lord, S.R.; Menz, H.B.; Steele, J.R. ISB Clinical Biomechanics Award 2009: Toe weakness and deformity increase the risk of falls in older people. Clin. Biomech. 2009, 24, 787–791. [Google Scholar] [CrossRef]
  11. Nix, S.E.; Vicenzino, B.T.; Collins, N.J.; Smith, M.D. Gait parameters associated with hallux valgus: A systematic review. J. Foot Ankle Res. 2013, 6, 9. [Google Scholar] [CrossRef] [PubMed]
  12. Kamonseki, D.H.; Gonçalves, G.A.; Yi, L.C.; Júnior, I.L. Effect of stretching with and without muscle strengthening exercises for the foot and hip in patients with plantar fasciitis: A randomized controlled single-blind clinical trial. Man. Ther. 2016, 23, 76–82. [Google Scholar] [CrossRef]
  13. Yokozuka, M.; Okazaki, K.; Sakamoto, Y.; Takahashi, K. Correlation between functional ability, toe flexor strength, and plantar pressure of hallux valgus in young female adults: A cross-sectional study. J. Foot Ankle Res. 2020, 13, 44. [Google Scholar] [CrossRef] [PubMed]
  14. Quinlan, S.; Fong Yan, A.; Sinclair, P.; Hunt, A. The evidence for improving balance by strengthening the toe flexor muscles: A systematic review. Gait Posture 2020, 81, 56–66. [Google Scholar] [CrossRef] [PubMed]
  15. Futrell, E.E.; Roberts, D.; Toole, E. The effects of intrinsic foot muscle strengthening on functional mobility in older adults: A systematic review. J. Am. Geriatr. Soc. 2022, 70, 531–540. [Google Scholar] [CrossRef] [PubMed]
  16. Jaffri, A.; Koldenhoven, R.; Saliba, S.; Hertel, J. Evidence of Intrinsic Foot Muscle Training in Improving Foot Function: A Systematic Review and Meta-analysis. J. Athl. Train. 2022, 58, 941–951. [Google Scholar] [CrossRef]
  17. de Souza, T.M.M.; de Oliveira Coutinho, V.G.; Tessutti, V.D.; de Oliveira, N.R.C.; Yi, L.C. Effects of intrinsic foot muscle strengthening on the medial longitudinal arch mobility and function: A systematic review. J. Bodyw. Mov. Ther. 2023, 36, 89–99. [Google Scholar] [CrossRef]
  18. Myerson, M.S.; Shereff, M.J. The pathological anatomy of claw and hammer toes. J. Bone Jt. Surg. 1989, 71, 45–49. [Google Scholar] [CrossRef]
  19. Bus, S.A.; Yang, Q.X.; Wang, J.H.; Smith, M.B.; Wunderlich, R.; Cavanagh, P.R. Intrinsic Muscle Atrophy and Toe Deformity in the Diabetic Neuropathic Foot: A magnetic resonance imaging study. Diabetes Care 2002, 25, 1444–1450. [Google Scholar] [CrossRef]
  20. Chung, K.W.; Suh, B.C.; Shy, M.E.; Cho, S.Y.; Yoo, J.H.; Park, S.W.; Moon, H.; Park, K.D.; Choi, K.G.; Kim, S.; et al. Different clinical and magnetic resonance imaging features between Charcot–Marie–Tooth disease type 1A and 2A. Neuromuscul. Disord. 2008, 18, 610–618. [Google Scholar] [CrossRef]
  21. Chang, R.; Kent-Braun, J.A.; Hamill, J. Use of MRI for volume estimation of tibialis posterior and plantar intrinsic foot muscles in healthy and chronic plantar fasciitis limbs. Clin. Biomech. 2012, 27, 500–505. [Google Scholar] [CrossRef] [PubMed]
  22. Soysa, A.; Hiller, C.; Refshauge, K.; Burns, J. Importance and challenges of measuring intrinsic foot muscle strength. J. Foot Ankle Res. 2012, 5, 29. [Google Scholar] [CrossRef] [PubMed]
  23. Stewart, S.; Ellis, R.; Heath, M.; Rome, K. Ultrasonic evaluation of the abductor hallucis muscle in hallux valgus: A cross-sectional observational study. BMC Musculoskelet. Disord. 2013, 14, 45. [Google Scholar] [CrossRef] [PubMed]
  24. Jastifer, J.R. Intrinsic muscles of the foot: Anatomy, function, rehabilitation. Phys. Ther. Sport. 2023, 61, 27–36. [Google Scholar] [CrossRef] [PubMed]
  25. Bryant, A.; Tinley, P.; Singer, K. Plantar pressure distribution in normal, hallux valgus and hallux limitus feet. Foot 1999, 9, 115–119. [Google Scholar] [CrossRef]
  26. Hara, Y.; Hara, N.; Matsudaira, K.; Oka, H. A comparison of muscle strength testing for great toe extension. J. Orthop. Sci. 2011, 16, 765–767. [Google Scholar] [CrossRef] [PubMed]
  27. Zhang, S.; Li, L. The differential effects of foot sole sensory on plantar pressure distribution between balance and gait. Gait Posture 2013, 37, 532–535. [Google Scholar] [CrossRef] [PubMed]
  28. Mickle, K.J.; Angin, S.; Crofts, G.; Nester, C.J. Effects of Age on Strength and Morphology of Toe Flexor Muscles. J. Orthop. Sports Phys. Ther. 2016, 46, 1065–1070. [Google Scholar] [CrossRef]
  29. Lee, P.-Y.; Tsai, Y.-J.; Liao, Y.-T.; Yang, Y.-C.; Lu, F.-H.; Lin, S.-I. Reactive balance control in older adults with diabetes. Gait Posture 2018, 61, 67–72. [Google Scholar] [CrossRef]
  30. de Win, M.M.L.; Theuvenet, W.J.; Roche, P.W.; de Bie, R.A.; van Mameren, H. The paper grip test for screening on intrinsic muscle paralysis in the foot of leprosy patients. Int. J. Lepr. Other Mycobact. Dis. 2002, 70, 16–24. [Google Scholar]
  31. Spink, M.J.; Fotoohabadi, M.R.; Menz, H.B. Foot and ankle strength assessment using hand-held dynamometry: Reliability and age-related differences. Gerontology 2010, 56, 525–532. [Google Scholar] [CrossRef] [PubMed]
  32. Ciesla, N.; Dinglas, V.; Fan, E.; Kho, M.; Kuramoto, J.; Needham, D. Manual Muscle Testing: A Method of Measuring Extremity Muscle Strength Applied to Critically Ill Patients. J. Vis. Exp. 2011, 50, e2632. [Google Scholar] [CrossRef]
  33. Bruening, D.A.; Ridge, S.T.; Jacobs, J.L.; Olsen, M.T.; Griffin, D.W.; Ferguson, D.H.; Bassett, K.E.; Johnson, A.W. Functional assessments of foot strength: A comparative and repeatability study. BMC Musculoskelet. Disord. 2019, 20, 608. [Google Scholar] [CrossRef]
  34. Wang, H.; Hile, E.; Ghazi, M. Apparatus and Method for Measuring Toe Flexion and Extension. U.S. Patent No. 11,402,284, 2 August 2022. [Google Scholar]
  35. Hile, E.S.; Ghazi, M.; Chandrashekhar, R.; Rippetoe, J.; Fox, A.; Wang, H. Development and Earliest Validation of a Portable Device for Quantification of Hallux Extension Strength (QuHalEx). Sensors 2023, 23, 4654. [Google Scholar] [CrossRef] [PubMed]
  36. Jamar Smart Hand Dynamometer. Available online: https://www.performancehealth.com/jamar-smart-hand-dynamometer (accessed on 11 July 2024).
  37. Yao, W.X. Motor-Unit Recruitment Plays an Important Role in Determining the Relationship Between Muscle Force and Force Variability. Biomed. J. Sci. Tech. Res. 2018, 8, 3. [Google Scholar] [CrossRef]
  38. Rodríguez-Rosell, D.; Pareja-Blanco, F.; Aagaard, P.; González-Badillo, J.J. Physiological and methodological aspects of rate of force development assessment in human skeletal muscle. Clin. Physiol. Funct. Imaging 2018, 38, 743–762. [Google Scholar] [CrossRef] [PubMed]
  39. Van Rossum, G.; Drake, F.L. Introduction to Python 3: Python Documentation Manual Part 1; CreateSpace: Scotts Valley, CA, USA, 2009. [Google Scholar]
  40. Singh, A.; Thakur, N.; Sharma, A. A review of supervised machine learning algorithms. In Proceedings of the 2016 3rd International Conference on Computing for Sustainable Global Development (INDIACom), New Delhi, India, 16–18 March 2016; pp. 1310–1315. [Google Scholar]
  41. Kumar, I.; Dogra, K.; Utreja, C.; Yadav, P. A Comparative Study of Supervised Machine Learning Algorithms for Stock Market Trend Prediction. In Proceedings of the 2018 Second International Conference on Inventive Communication and Computational Technologies (ICICCT), Coimbatore, India, 20–21 April 2018; pp. 1003–1007. [Google Scholar]
  42. Shetty, S.H.; Shetty, S.; Singh, C.; Rao, A. Supervised Machine Learning: Algorithms and Applications. In Fundamentals and Methods of Machine and Deep Learning; John Wiley & Sons, Ltd.: Hoboken, NJ, USA, 2022; pp. 1–16. [Google Scholar] [CrossRef]
  43. Laaksonen, J.; Oja, E. Classification with learning k-nearest neighbors. In Proceedings of the International Conference on Neural Networks (ICNN’96), Washington, DC, USA, 3–6 June 1996; Volume 3, pp. 1480–1483. [Google Scholar] [CrossRef]
  44. Mahato, V.; O’Reilly, M.; Cunningham, P. A Comparison of k-NN Methods for Time Series Classification and Regression. In Proceedings of the 26th AIAI Irish Conference on Artificial Intelligence and Cognitive Science, Dublin, Ireland, 6–7 December 2018. [Google Scholar]
  45. Taunk, K.; De, S.; Verma, S.; Swetapadma, A. A Brief Review of Nearest Neighbor Algorithm for Learning and Classification. In Proceedings of the 2019 International Conference on Intelligent Computing and Control Systems (ICCS), Madurai, India, 15–17 May 2019; pp. 1255–1260. [Google Scholar] [CrossRef]
  46. Belgiu, M.; Drăguţ, L. Random forest in remote sensing: A review of applications and future directions. ISPRS J. Photogramm. Remote Sens. 2016, 114, 24–31. [Google Scholar] [CrossRef]
  47. Zhang, X. Support Vector Machines. In Encyclopedia of Machine Learning and Data Mining; Sammut, C., Webb, G.I., Eds.; Springer: Boston, MA, USA, 2017; pp. 1214–1220. [Google Scholar] [CrossRef]
  48. Fawcett, T. An introduction to ROC analysis. Pattern Recognit. Lett. 2006, 27, 861–874. [Google Scholar] [CrossRef]
  49. Abe, T.; Tayashiki, K.; Nakatani, M.; Watanabe, H. Relationships of ultrasound measures of intrinsic foot muscle cross-sectional area and muscle volume with maximum toe flexor muscle strength and physical performance in young adults. J. Phys. Ther. Sci. 2016, 28, 14–19. [Google Scholar] [CrossRef]
  50. Nagano, K.; Okuyama, R.; Taniguchi, N.; Yoshida, T. Gender difference in factors affecting the medial longitudinal arch height of the foot in healthy young adults. J. Phys. Ther. Sci. 2018, 30, 675–679. [Google Scholar] [CrossRef]
  51. Kawamori, N.; Rossi, S.J.; Justice, B.D.; Haff, E.E.; Pistilli, E.E.; O’bryant, H.S.; Stone, M.H.; Haff, G.G. Peak force and rate of force development during isometric and dynamic mid-thigh clean pulls performed at various intensities. J. Strength. Cond. Res. 2006, 20, 483. [Google Scholar] [PubMed]
  52. Andersen, L.L.; Aagaard, P. Influence of maximal muscle strength and intrinsic muscle contractile properties on contractile rate of force development. Eur. J. Appl. Physiol. 2006, 96, 46–52. [Google Scholar] [CrossRef] [PubMed]
  53. Peñailillo, L.; Blazevich, A.; Numazawa, H.; Nosaka, K. Rate of force development as a measure of muscle damage. Scand. J. Med. Sci. Sports 2015, 25, 417–427. [Google Scholar] [CrossRef] [PubMed]
  54. Farup, J.; Rahbek, S.K.; Bjerre, J.; de Paoli, F.; Vissing, K. Associated decrements in rate of force development and neural drive after maximal eccentric exercise. Scand. J. Med. Sci. Sports 2016, 26, 498–506. [Google Scholar] [CrossRef]
  55. Kamasaki, T.; Otao, H.; Tanaka, S.; Hachiya, M.; Kubo, A.; Okawa, H.; Sakamoto, A.; Fujiwara, K.; Suenaga, T.; Kichize, Y.; et al. Age-specific comparisons in the rate of force development of toe pressure strength and its association with the timed up and go test. Eur. Geriatr. Med. 2024, 1–10. [Google Scholar] [CrossRef] [PubMed]
  56. Sarikaya, F.; Sahin, M. The Effect of Big Toe Strength Development on Some Athletic Performance Parameter in Young Male Footballers. Pak. J. Med. Health Sci. 2022, 16, 997. [Google Scholar] [CrossRef]
  57. Arnold, P.; Vantieghem, S.; Gorus, E.; Lauwers, E.; Fierens, Y.; Pool-Goudzwaard, A.; Bautmans, I. Age-related differences in muscle recruitment and reaction-time performance. Exp. Gerontol. 2015, 70, 125–130. [Google Scholar] [CrossRef] [PubMed]
  58. Bohannon, R.W. Manual muscle testing: Does it meet the standards of an adequate screening test? Clin. Rehabil. 2005, 19, 662–667. [Google Scholar] [CrossRef] [PubMed]
  59. Sallinen, J.; Stenholm, S.; Rantanen, T.; Heliövaara, M.; Sainio, P.; Koskinen, S. Hand-Grip Strength Cut Points to Screen Older Persons at Risk for Mobility Limitation. J. Am. Geriatr. Soc. 2010, 58, 1721–1726. [Google Scholar] [CrossRef]
  60. Siqueira, V.A.A.A.; Sebastião, E.; Camic, C.L.; Machado, D.R.L. Higher Body Mass Index Values Do Not Impact Physical Function and Lower-Extremity Muscle Strength Performance in Active Older Individuals. Int. J. Exerc. Sci. 2022, 15, 330–340. [Google Scholar]
  61. Kim, M.-J.; Seino, S.; Kim, M.-K.; Yabushita, N.; Okura, T.; Okuno, J.; Tanaka, K. Validation of lower extremity performance tests for determining the mobility limitation levels in community-dwelling older women. Aging Clin. Exp. Res. 2009, 21, 437–444. [Google Scholar] [CrossRef] [PubMed]
  62. Kusagawa, Y.; Kurihara, T.; Imai, A.; Maeo, S.; Sugiyama, T.; Kanehisa, H.; Isaka, T. Toe flexor strength is associated with mobility in older adults with pronated and supinated feet but not with neutral feet. J. Foot Ankle Res. 2020, 13, 55. [Google Scholar] [CrossRef] [PubMed]
  63. Huang, J.; Ling, C.X. Using AUC and accuracy in evaluating learning algorithms. IEEE Trans. Knowl. Data Eng. 2005, 17, 299–310. [Google Scholar] [CrossRef]
Figure 1. Measurement of GTES using ToeScale (Left); parameters selected based on muscle performance to characterize GTES force–time curve (Right).
Figure 1. Measurement of GTES using ToeScale (Left); parameters selected based on muscle performance to characterize GTES force–time curve (Right).
Sensors 24 04841 g001
Table 1. Demographics of the participants.
Table 1. Demographics of the participants.
VariableTotal SampleOlder AdultsYounger Adultsp-ValueMalesFemalesp-Value
Sample size311714NA922NA
Weight (Kg)65.29 (13.63)67.88 (15.05)62.14 (10.99)0.25077.06 (14.38)60.47 (10.13)0.002
Height (m)1.67 (0.10)1.67 (0.11)1.66 (0.10)0.8141.78 (0.09)1.62 (0.09)<0.001
BMI (Kg/m2)23.31 (3.47)24.04 (3.44)22.43 (3.42)0.20324.15 (3.68)22.97 (3.41)0.400
All values of demographics are presented as means (standard deviation).
Table 2. Sex- and age-based differences in GTES measures and GS.
Table 2. Sex- and age-based differences in GTES measures and GS.
All VariablesAllMalesFemalesp-Value
Peak GTES (N)Total Sample42.89 (15.47)54.82 (13.06)38.01 (13.82)0.004
Older39.32 (17.25)58.02 (18.09)33.57 (12.57)
Younger47.22 (12.22)52.26 (8.79)44.42 (13.39)
Average GTES (N)Total Sample34.78 (13.15)42.45 (10.61)31.64 (12.98)0.04
Older31.58 (13.64)44.42 (13.62)27.63 (11.39)
Younger38.67 (11.84)40.88 (8.88)37.44 (13.55)
Rise Time (s)Total Sample2.29 (1.94)1.02 (0.41)2.82 (2.09)0.02
Older2.94 (2.22)1.11 (0.62)3.5 (2.23)
Younger1.52 (1.21)0.96 (0.17)1.83 (1.44)
Rate of force development (RFD in N/s)Total Sample28.64 (21.80)46.87 (14.76)21.18 (19.89)0.002
Older21.79 (20.09)49.17 (19.59)13.37 (12.21)
Younger36.95 (20.82)45.02 (11.74)32.47 (23.91)
Above Avg GTES (%)Total Sample42.59 (13.53)50.22 (11.59)39.48 (13.24)0.04
Older36.15 (11.37)42.45 (10.61)34.21 (11.27)
Younger50.42 (11.96)56.44 (8.69)47.08 (12.63)
GS_N (N)Total Sample259.14 (100.20)374.85 (66.11)211.81 (67.77)<0.001
Older239.99 (93.56)355.37 (89.58)204.50 (67.76)
Younger282.39 (103.26)390.44 (45.17)222.36 (70.39)
Table 3. Correlation between GTES parameters, GS, and BMI.
Table 3. Correlation between GTES parameters, GS, and BMI.
Variables Whole Sample a,bOlder Adults aYounger Adults b
GSBMIGSBMIGSBMI
Peak GTES0.545 *0.390 *0.519 *0.594 *0.546 *0.297
Average GTES0.512 *0.3010.516 *0.513 *0.4450.219
Rise Time−0.431 *0.143−0.3240.118−0.451−0.103
RFD0.568 *0.0040.473 ^0.1520.4030.133
GS10.15510.4141−0.012
BMI0.15510.4141−0.0121
a: Lack of normality in RFD; b: lack of normality in rise time; a,b: lack of normality in rise time and RFD; *: statistically significant; ^: trending towards statistical significance.
Table 4. Accuracy and AUC scores for the different ML classifiers.
Table 4. Accuracy and AUC scores for the different ML classifiers.
ModelTarget VariableValidation Accuracy (%)Test Accuracy (%)AUC
Support vector machine (SVM)Age62.566.670.72
Sex7566.670.14
K-nearest neighbors (k-NN, k = 5)Age62.566.670.75
Sex87.555.560.5
K-nearest neighbors (k-NN, k = 10)Age62.566.670.5
Sex7577.780.36
Random forest (RF)Age62.566.670.67
Sex10055.560.46
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

Chandrashekhar, R.; Perez, L.F.; Wang, H. Characterization of Great Toe Extension Strength Using ToeScale—A Novel Portable Device. Sensors 2024, 24, 4841. https://doi.org/10.3390/s24154841

AMA Style

Chandrashekhar R, Perez LF, Wang H. Characterization of Great Toe Extension Strength Using ToeScale—A Novel Portable Device. Sensors. 2024; 24(15):4841. https://doi.org/10.3390/s24154841

Chicago/Turabian Style

Chandrashekhar, Raghuveer, Luciana Fonseca Perez, and Hongwu Wang. 2024. "Characterization of Great Toe Extension Strength Using ToeScale—A Novel Portable Device" Sensors 24, no. 15: 4841. https://doi.org/10.3390/s24154841

APA Style

Chandrashekhar, R., Perez, L. F., & Wang, H. (2024). Characterization of Great Toe Extension Strength Using ToeScale—A Novel Portable Device. Sensors, 24(15), 4841. https://doi.org/10.3390/s24154841

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

Article Metrics

Back to TopTop