Ambient floor vibration sensing advances the accessibility of functional gait assessments for children with muscular dystrophies

Nature

Ambient floor vibration sensing advances the accessibility of functional gait assessments for children with muscular dystrophies"


Play all audios:

Loading...

ABSTRACT Muscular dystrophies (MD) are a group of genetic neuromuscular disorders that cause progressive weakness and loss of muscles over time, influencing 1 in 3500–5000 children


worldwide. New and exciting treatment options have led to a critical need for a clinical post-marketing surveillance tool to confirm the efficacy and safety of these treatments after


individuals receive them in a commercial setting. For MDs, functional gait assessment is a common approach to evaluate the efficacy of the treatments because muscle weakness is reflected in


individuals’ walking patterns. However, there is little incentive for the family to continue to travel for such assessments due to the lack of access to specialty centers. While various


existing sensing devices, such as cameras, force plates, and wearables can assess gait at home, they are limited by privacy concerns, area of coverage, and discomfort in carrying devices,


which is not practical for long-term, continuous monitoring in daily settings. In this study, we introduce a novel functional gait assessment system using ambient floor vibrations, which is


non-invasive and scalable, requiring only low-cost and sparsely deployed geophone sensors attached to the floor surface, suitable for in-home usage. Our system captures floor vibrations


generated by footsteps from patients while they walk around and analyzes such vibrations to extract essential gait health information. To enhance interpretability and reliability under


various sensing scenarios, we translate the signal patterns of floor vibration to pathological gait patterns related to MD, and develop a hierarchical learning algorithm that aggregates


insights from individual footsteps to estimate a person’s overall gait performance. When evaluated through real-world experiments with 36 subjects (including 15 patients with MD), our floor


vibration sensing system achieves a 94.8% accuracy in predicting functional gait stages for patients with MD. Our approach enables accurate, accessible, and scalable functional gait


assessment, bringing MD progressive tracking into real life. SIMILAR CONTENT BEING VIEWED BY OTHERS AGE AND ENVIRONMENT-RELATED DIFFERENCES IN GAIT IN HEALTHY ADULTS USING WEARABLES Article


Open access 30 September 2020 IN-CLINIC AND NATURAL GAIT OBSERVATIONS MASTER PROTOCOL (I-CAN-GO) TO VALIDATE GAIT USING A LUMBAR ACCELEROMETER Article Open access 29 August 2024 MONITORING


ACTIVITY AND GAIT IN CHILDREN (MAGIC) USING DIGITAL HEALTH TECHNOLOGIES Article Open access 21 March 2024 INTRODUCTION Muscular dystrophies (MD) are a group of neuromuscular disorders that


commonly present with muscle weakness and atrophy and result in motor and gait impairments of varying degrees. MDs are present in 1 in 3500–5000 children worldwide, depending on the


type1,2,3. While there are no cures available for the spectrum of MDs, treatments such as corticosteroid therapy and proactive cardiac and respiratory intervention have been evidenced to


delay the progression of the disease and can extend a child’s lifespan4,5. In recent years, the therapeutic landscape has been quickly evolving with the promise of various therapeutic


modalities making their way through the clinical trial pipeline. However, the cycle of therapeutic development can be long, and long-term effectiveness is difficult to assess after


conditional approval of their usage; long-term monitoring is critical to expand the accessibility of these treatments to all patients. For example, with the recent accelerated approval of


Elevidys, a one-time gene replacement therapy for Duchenne muscular dystrophy (DMD) that has been shown to improve gross motor skill, there is an urgent unmet need for a way to collect


functional gait outcome data on children who have received this gene therapy commercially. As Elevidys is a one-time infusion, there is little incentive for the family to continue to come


for follow-up visits6,7. Additionally, there is a lack of access to specialty centers with experts who are trained to administer disease-specific assessments, limiting the ability to track


the impact of treatment over time, especially for low-income families. To this end, a monitoring system that passively tracks the progression of MD at children’s homes to assess their


functional gait through the observation of gait symptoms can accelerate the post-approval process, closing the cycle of treatment development. Previous studies have developed both clinical


assessments and sensing technologies to monitor gait health in patients with MD. Existing clinical practice in tracking the progression of MD is by measuring the patient’s functional


abilities, including walking/running speed or ability to do common activities such as climbing stairs8,9. However, these assessments require in-person appointments at specialized clinics


(around 150 in the U.S.), which may not be accessible to low-income families or those who live in rural areas. Therefore, a system that can monitor patients in their homes is needed for more


frequent and continuous monitoring of either MD progression and/or treatment effect. To achieve this, several existing sensing technologies are available, including force/pressure mat10,


wearable devices11, and camera-based systems12; however, they have either limited spatial coverage, are unable to run for a long period, or have limited kinetic information. For example,


force/pressure sensors require dense deployment due to their restricted sensing range; wearables require patients to carry devices all the time, which is often challenging for children;


cameras require clear lines of sight and lack kinetic information on how the forces act and transmit through the body. They also raise privacy concerns when installed at home. These


limitations make such technologies less practical and inadequate for continuous monitoring in daily life. In this study, we introduce a novel framework based on sensing ambient floor


vibrations to monitor gait health in patients with MD. The physical mechanism behind this approach is that as a person walks and steps on the floor, each footstep exerts a force at the floor


surface that generates vibration waves. By capturing and analyzing these waves through vibration sensors mounted on the floor, the characteristics of a person’s gait can be inferred and


various gait symptoms related to MD can be identified, as discussed in a previous study13. For example, waddling gait is commonly observed among children with MD, which is characterized by


the sway of the body from side to side and hip drops with each step14,15. This leads to slower, unstable walking that is reflected in floor vibration through larger intervals between the


vibration impulses and larger variances among a series of continuous footstep signals. The main advantages of our approach include high scalability, low cost/maintenance, contactless data


collection, and wide coverage (up to 20 m distance as evaluated in previous work using the same sensor type16), leading to more accessible functional gait assessments in patients’ homes.


Furthermore, it is perceived as more privacy-friendly, and thus suitable for in-home usage. The main research challenges to relate the signal patterns of floor vibration to pathological gait


patterns in patients with MD, mainly lie in two aspects: (1) interpretability and (2) complex influencing factors in gait. First, unlike camera and force plate measurements, vibration


signals do not provide direct observations of the motion and force in a person’s gait. Therefore, it is necessary to analyze and interpret the vibration signals in terms of gait


characteristics to produce clinical insights. Secondly, one unique challenge in long-term continuous gait monitoring is the variability in walking patterns due to a complex mixture of


reasons in daily life. For example, gait patterns are not only influenced by neuromuscular disorders, but also by a person’s energy level, emotional status, and environmental


disturbances17,18,19. As a result, it is difficult to incorporate all these factors when assessing an individual’s gait, which could lead to erroneous estimations of functional outcomes for


clinical trials. To overcome these challenges, we develop our framework to (1) improve the interpretability of vibration signals by characterizing and extracting gait symptoms related to MD


from floor vibration data (discussed in Sect. 2.2), and (2) enhance its robustness to the complex influencing factors in gait by formalizing and integrating multiple levels of gait and


biometric features from an individual through a hierarchical deep-learning model to make a collective decision (discussed in Sect. 2.3). Specifically, we first extract the gait features that


explicitly inform symptoms related to MD, including cadence, symmetry, and initial contact types (see Sect. 2.2). Then, these explicit gait symptom-based features are combined with the


implicit signal-based features (e.g., dominant frequencies, power spectral density, energy variability) to make a decision collaboratively. To reduce fluctuations in our prediction of gait


health due to the complex influencing factors, we leverage the power of data aggregation and develop a model with a hierarchical structure that aggregates the latent representations of all


footstep signals from a person. This allows the model to capture the overall gait pattern of a person instead of focusing on one single footstep. Specifically, our model first aggregates


features from individual footsteps to a footstep trace (which consists of a series of consecutive footsteps), then combines the latent features from multiple footstep traces to produce a


representative walking pattern of a person. After each level of aggregation, new features extracted from the current hierarchy are concatenated with the aggregated features from the previous


hierarchy, which captures the variability and inter-dependencies between individual footsteps or traces. This provides additional information on gait balance and symmetry, which are


important aspects of gait health. We evaluate the framework through three rounds of walking experiments with 36 human subjects. The first round is a lab-based walking study to test the


feasibility of floor vibration in capturing MD gait symptoms; The second and third rounds are conducted at a children’s hospital, to evaluate the performance of our sensing system with MD


specialists and patients. Among all human subjects, 15 of which are children with various types of MD, including Duchenne, Becker, and Limb-Girdle MD. The rest of the subjects are healthy


participants, including siblings of these children as well as adult volunteers. Our floor vibration sensing system achieved an average accuracy of 94.8% in tracking progression stages


defined based on the 100-m run time measured during standard functional assessments in the hospital20, which is one of the most important references to understand the functional ability of


an individual with MD. RESULTS EVALUATION OF THE AMBIENT FLOOR VIBRATION SENSING METHOD In order to evaluate the performance of the floor vibration sensing system in laboratory and real-life


settings, we recruited human subjects (\(N=36\)) and conducted experiments at a university lab and a children’s hospital with healthy human subjects (\(N=21\)) and children with MD


(\(N=15\)). The experiments consist of two phases - Phase 1 is a pilot study to test the feasibility of ambient floor vibration sensing in capturing gait characteristics in lab settings


(Fig. 1 left column); Phase 2 has two hospital studies to evaluate our sensing method in real life (Fig. 1 middle and right columns). The phase 1 lab study aims to explore the feasibility of


using floor vibration signals in estimating gait parameters and detecting abnormal gait characteristics related to MD. We measured the normal gait and simulated abnormal gait


characteristics related to MD from adult healthy participants (\(N=10\)) in a laboratory setting at the university. During the experiment, we installed four geophone sensors at the edge of a


7-meter-long walking platform, spaced 2 m apart (Fig. 1a), to capture the floor vibration induced by human gait. The sensor placement was designed to optimize the area of coverage and


signal quality, as well as to provide redundancy in data collection and analysis. We also recorded the gait kinematics through the VICON Motion Capture system with 10 infrared cameras as the


ground truth21, which has a less than 2mm measurement error as reported by existing studies22,23. The kinematics data were processed through manual labeling of gait cycles (i.e., foot


strike and foot off time) and Plug-In Gait processing pipelines to compute the gait parameters24. Each participant walked back and forth on the platform for 20 trials, first with their


natural gait on their own shoes, and then walking with simulated abnormal gait patterns that are commonly observed in patients with MD, including slow walking, asymmetrical walking, and


toe/midfoot strike for 10–15 trials. The simulated walking trials were instructed by medical experts from gait clinics to ensure they were realistic. By analyzing the floor vibration data,


our approach has a root-mean-square error (RMSE) of 0.05 s (\(\sim 5\)%) in estimating the step time and 0.15 m (\(\sim 15\)%) in estimating the step length. The error rates in estimating


these spatiotemporal parameters are satisfactory and comparable to the state-of-the-art wearable devices11, which will be discussed further in Sect. 3. The accuracy for gait abnormality


detection is up to 93% after testing on a data-driven model trained through frequency-domain features from the vibration signals. We conducted the phase 2 study at the children’s hospital


and evaluated our system in a real-life setting along a hospital corridor. The participants include patients with MD (\(N=15\), 11 male and 4 female, age = 7–15 years, with \(N_{DMD}=11\),


\(N_{BMD}=2\), \(N_{LGMD}=2,\) for Duchenne, Becker, and Limb-Girdle MD, respectively) and other healthy subjects (\(N=11\)) such as the patient’s healthy siblings and the staff at the


hospital. The healthy adults are considered to approximate teenagers who typically have similar walking patterns as the adults. To explore different sensor layouts, we deployed the system in


two rounds, one with eight sensors placed in a straight line at one side of the corridor with 1 m apart, and another with five sensors mounted at both sides of the corridor, spaced with 2-m


offsets (Fig. 1a). The sensor placement was significantly denser than required to provide redundancy in data collection and analysis. In both settings, 3–5 cameras were mounted around the


sensing area, aiming at the lower body of the participants to collect the ground truth of their gait patterns. Each participant walked along the corridor back and forth for 5–10 rounds using


their natural gait with their choice of footwear. For young children who have a high risk of falling, their parents walked along with them to provide timely assistance. The vibration


signals generated by the parent were separated from the child through a recursive blind source separation algorithm developed in prior work25, in which the parent-only walking data were


collected first as a template, and was then separated from the combined signal when walking with the child. To evaluate the performance of the floor vibration sensing system, a unified scale


for MD progression was defined based on the 100-m run time measured during standard functional assessments in the hospital20, which is one of the most important references to understand the


functional ability of a patient. The scale divides the normative 100 m run time % into 8 functional stages (from Stage 0 to 7) based on their distinctive clinical interpretations, which is


presented in Sect. 4.2. Since patients in the last two stages typically require walking assistance, our floor vibration sensing system estimates the functional stages from 0 to 5 for each


subject. The distribution of stages among the subjects is—five participants in Stage 1, four participants in Stage 2, one participant in Stage 3, three participants in Stage 4, and two


participants in Stage 5. Our system achieves up to 94.8% test accuracy in classifying the functional stages using the data from 3 sensors. Using only one sensor (with the best data quality)


still leads to more than 90% accuracy for MD functional stage prediction, which means that the number of sensors can be reduced significantly in practice. The second sensor layout setting


has a slightly higher accuracy (\(\sim 3\%\)) than the first one because it captures more accurate spatial information of the gait when placing sensors at both sides. CHARACTERIZATION OF


GAIT PATTERNS USING FLOOR VIBRATION DATA To translate the floor vibration signals into gait health insights, we develop gait symptom-based features based on the vibration signals that


explicitly inform gait parameters and health indicators (e.g., step time, cadence, initial contact type), as summarized in Fig. 2. The method to extract these symptoms is discussed in Sect. 


4.4. In addition, we further extract signal-based features (e.g., frequency spectrum, signal energy) that represent the implicit patterns that are helpful yet undefined in existing gait


assessments. By combining both explicit and implicit features, we advance our data-driven model using neural networks, which establish the complex nonlinear relationships between the


features and the gait (Fig. 3). The data-driven model predicts the functional stages of individuals with MD by encoding the information from all the features. Evaluation results show that


the combination of features produces a \(2.1\times\) to \(5.9\times\) error reduction compared to models with symptom-based or signal-based features only. The combined feature has a 94.8%


accuracy, while the model with only signal-based or only symptom-based features has an average of 64.4% and 83.7% accuracy, respectively. The extracted gait symptom-based features include


step time, cadence, step time variability, left–right symmetry, and initial contact type. We estimated the step time as the duration between the foot strike impulse from one leg and the


following impulse resulting from the contralateral leg and calculated the cadence by counting the number of foot strike-induced impulses within every minute (Fig. 2a). Both features (step


time and cadence) are used to indicate how fast a person walks as numerous previous studies suggest that one significant sign of early-stage MD is the decrease in cadence and increase in


step time26. We also estimated the step time variability through the standard deviation of the step time within each walking trace. This metric is found to be correlated to the balance of


the gait27,28. In addition, severe left–right asymmetry has been previously observed in patients with MD in previous studies29, which was helpful in determining the need for assistive


equipment for the patient in daily walking. In this study, we extracted the symmetry metric by computing the cosine distance between the frequency spectrum of the left and right foot, which


compares the relative frequency distribution between these feet normalized by their corresponding foot strike energy (Fig. 2b). Finally, we predicted the probability of each initial contact


type (toe vs. flatfoot vs. heel contact) by training on the data collected in the laboratory setting (Fig. 2c). Clinical studies have found that toe-walking, calf hypertrophy, and using the


Gower’s maneuver to get up off of the floor are common early signs of MD. During gait assessments, the observation of abnormal initial contact (e.g., flatfoot and toe contact) with a wider


base of support is commonly considered as a sign of MD progression30. When compared with the ground truth, the extracted symptom-based features demonstrated promising results of 0.028 s and


4.88 step/min mean absolute errors (MAE) for step time and cadence estimation, respectively, and 90.2% and 89.8% average precision in detecting asymmetry and toe/midfoot initial contacts,


respectively (Fig. 2d). The signal-based features include basic signal statistics, the dominant frequency at foot strike and foot off, power spectral density (frequency spectrum), and energy


variability. The basic signal statistics include the mean, standard deviation, skewness, and kurtosis of the time-domain vibration signals from each footstep. These statistics provide an


overview of signal patterns from various aspects, including intensity, variability, distribution patterns, and the proportion of extreme values. Then, we detected the dominant frequency at


foot strike and foot off to gain insights into the ground reaction forces during the contact. As discussed in an existing study using floor vibration sensing31, a higher dominant frequency


at the foot strike corresponds to frictional forces and a smaller contact area while the lower frequency indicates vertical forces and a larger contact area. The dominant frequency at toe


push-off also indicates the power of the ankle plantarflexion (extension). The power spectral density is a spectrum of the signal’s power content versus frequency. It describes the power


distribution over frequency normalized by the spectral resolution employed to digitize the signal, which has been shown to be representative in describing the implicit gait-related features


encoded in various frequency components13. In addition, we computed the energy variability among a series of footsteps to describe the overall variability of a person’s footstep forces while


walking because a stronger footstep force typically leads to a larger signal energy based on the elastic theory. Through evaluation, we found that signal-based features provide rich gait


information on top of the symptom-based features, boosting the overall accuracy from 83.7 to 94.8%. MODELING HIERARCHICAL GAIT FEATURES FOR MD FUNCTIONAL STAGE PREDICTION We developed and


evaluated our hierarchical feature aggregation model to overcome the gait variability challenge induced by a complex mixture of physical and psychological influencing factors in daily life.


We observed that a person’s gait pattern is hierarchical in nature—there are features describing individual footsteps (e.g., step time), features characterizing a trace of continuous


footsteps (e.g., step variability), and factors that influence the overall pattern of a person’s gait (e.g., leg length, weight). Therefore, we incorporated this information by designing a


hierarchical neural network that first integrates features from individual footsteps to a footstep trace, then combines the latent features from multiple footstep traces and a person’s


unique biometrics to produce a representative feature set for that person’s gait. The benefit of the hierarchical architecture is to prompt the model to overcome the sampling bias among the


participants by learning MD stages first through their gait characteristics and then through their biometrics. Given that there are unbalanced samples among various age groups, gender, body


configurations, MD types, and so on, directly learning from all the features together may create artificial bias when estimating model parameters for MD stage assessments (e.g., the age may


be over-emphasized because children with younger age tend to be at earlier stages of MD). By leveraging the domain knowledge of feature hierarchy and emphasizing the gait characteristics


before considering the biometrics, we enable the hierarchical model to mitigate the effect of sampling bias by having the model learn from the gait features first. This makes the model more


generalizable to other populations including previously unrecorded people. Specifically, we categorized the symptom-based and signal-based features into two levels of hierarchy, including


step-level and trace-level features, and then combined these with a person’s biometrics to predict the functional stage of MD (Fig. 3). The step-level features were extracted from individual


footsteps, including the step time and initial contact type (symptom-based), as well as the basic signal statistics, dominant frequencies, and power spectral density (signal-based). The


trace-level features were also computed based on a continuous series of footsteps, including the left–right symmetry, step time variability, cadence (symptom-based), signal energy


variability among all footsteps, and the power spectral density of the most representative footstep (i.e., has the highest cumulative energy without clipping) of the entire trace


(signal-based). The person-level features were obtained from medical records, mainly consisting of biometrics such as height, weight, age, and gender. At each level of the hierarchy, we


utilized a multi-layer neural network to learn the embeddings of the features through training and testing on separated datasets. The training dataset consists of 80% of the randomly sampled


footsteps, and the test dataset consists of the remaining 20%. The detailed neural network architecture and training procedure are introduced in Sect. 4.5. The confusion matrix and feature


plots in Fig. 4 summarize the precision of footsteps/traces belonging to various functional stages under cross-validation on the test dataset, where the diagonal boxes show the percentage of


correct predictions among all predicted values. We show that the hierarchical feature aggregation model is very effective in reducing false positives and mitigating the influence of the


confounding factors—It increases the MD functional stage prediction accuracy from 73.5 (step level) to 84.2% (trace level), and finally to 94.8% at the person-level prediction (\(\sim


5\times\) error reduction). DISCUSSION ADVANTAGES OF AMBIENT FLOOR VIBRATION SENSING FOR FUNCTIONAL GAIT ASSESSMENTS The ambient floor vibration sensing approach meets the requirements for


functional gait assessment in patient’s home settings, providing accessible and accurate monitoring of gait health for individuals with MD. The floor vibration sensing system utilizes


low-cost and portable geophone sensors attached to the floor surface that passively capture the gait-induced vibrations as a person walks by. This approach is contactless, non-interruptive,


and unobtrusive, allowing long-term and continuous gait health monitoring in daily life. Our evaluation demonstrates that this sensing system can accurately estimate various gait parameters,


infer gait symptoms, and produce quantitative and interpretable predictions on progressive stages of MD. The system was evaluated with a diverse group of subjects in terms of age, gender,


and MD types, showing its potential to be extended to other diseases that involve gait disorders. The floor vibration sensing approach has comparable error rates as the state-of-the-art


sensing technologies while being more suitable for continuous and long-term gait monitoring at home. Previous studies have explored video cameras, force plate/pressure mats, wearable


devices, and radio-frequency-based devices. These systems typically have around 0.01–0.1 s and 1–20 cm of error in temporal and spatial parameter estimation10,11,23. For comparison, the


floor vibration sensing approach has an average of 0.05 s and 25 cm error for temporal and spatial parameter estimation, respectively. While the vibration sensing approach has limited


spatial performance due to the interference of the floor structures, it has satisfactory accuracy in extracting temporal information and significant operational benefits, including having a


larger area of coverage (up to 20 m), not carrying devices, being contactless and more privacy friendly. Therefore, this approach is suitable for in-home functional gait assessments that


require acceptable accuracy while being more convenient and can operate in a longer term. To this end, it can advance the accessibility of functional gait assessment for low-income families


or families living in areas where specialized clinics are unavailable. This will accelerate the treatment development cycle, increasing the enrollment rate while reducing the cost of


post-approval studies. ANALYSIS OF FEATURE TRENDS WITH MD FUNCTIONAL STAGES Analysis results demonstrate that symptom-based features have consistent trends: as the MD stage increases, (1)


step frequency first increases and then decreases, (2) the probability of toe contact increases, and (3) the symmetry score decreases (Fig. 5). In the following paragraphs, we discuss the


trends of step time, cadence, probability of toe contact, and symmetry score to show that our approach is interpretable in terms of these gait symptoms. Existing studies found that as


individuals with Duchenne muscular dystrophy moved from the early to late phase, the gait pattern demonstrated decreased walking velocity and cadence, lack of heel contact during the stance


phase, and an increased foot drop in the swing that leads to instability32,33. The symptom-based features from our study have consistent trends as the above-mentioned results. As the MD


progresses, step time and cadence extracted from floor vibration indicate that the subjects appear to have an increasing trend of step frequency at the beginning and then a decreasing trend


as the stage increases, which may be due to the change in initial contact type from heel to toe (Fig. 5a, b). For example, the slight increase in cadence may be caused by the alternation of


gait from heel to toe strike which typically has a shorter contact time. As the MD stage increases further, the decrease in cadence may be due to the further degeneration of leg muscles,


making the toe-walking much slower34,35. However, it is worth noting there is only one subject in stage 3, who has a fast walking habit, which may also lead to a high cadence/short step time


and small variance in the fourth bar. In addition, the majority of the healthy participants recorded are adults, who typically have longer step times than children, resulting in longer step


times and lower cadence among the stage 0 samples. Therefore, the trends between step time/cadence and MD stages may require more experiments to validate in the future. The probability of


toe contact increases and the symmetry score decreases as the MD stage increases, which are visualized through the scatter plot of individual footstep samples (Fig. 5c and d). The figure


shows the estimation value of each sample because the extreme values (samples out of three standard deviations) are also representative of gait health in terms of MD stages. Overall, the


estimated mean probability of toe contact significantly increases as the MD stage increases (Fig. 5c). This observation is consistent with previous clinical studies36,37, which found that


toe-walking is a common symptom in patients with MD, especially after the initial stage. It is worth noting that the number of footsteps with high probabilities also increases, indicating


that more footsteps are likely to be toe contacts in patients with MD. In addition, the estimated symmetry score gradually decreases as MD progresses (Fig. 5d), which is also consistent with


the previous findings38,39. In this case, the number of footsteps with high symmetry scores decreases significantly as the stage increases, meaning that fewer left–right footstep pairs are


symmetrical in patients with MD. DISCUSSION ON THE EFFECTS OF MD TYPES AND SENSOR LOCATIONS The vibration data pattern observed from individuals with various MD types aligns with the


clinical understanding of the differences among MD types (Fig. 5e). For example, existing studies have found the Limb-Girdle MD typically has a slower expected disease progression compared


to Duchenne MD and Becker MD40. When plotting the data from individuals of similar ages (12–14 years old), we observe that there is little deviation between the data from the patients with


Limb-Girdle MD (dark blue color) and the data from the healthy children (orange color). In contrast, the data from Duchenne MD (light blue color) forms a distinct cluster from the others as


it has a significant influence on the shank, which causes more observable changes in gait. While Becker MD (gray color) also affects the shank, it typically has less severe symptoms than


Duchenne MD (light blue color), making a proportion of the data closer to the healthy gait (orange color) yet still distinguishable from the other types. Although the study explored various


MD stages and types, it is pertinent to note the relatively small number of subjects within the later stages among the Becker and Limb-Girdle MD subgroups. This highlights the potential for


further research to offer a more exhaustive exploration of gait-induced floor vibrations within these groups. In addition, the effect of sensor locations on vibration data can be observed


from the data distribution shifts across various sensors (Fig. 5f). The difference across sensors can come from three sources, summarized from a few existing studies41,42: (1) floor


heterogeneity during vibration wave propagation, (2) location-dependent environmental noises, and (3) hardware variations (e.g., fabrication quality, sensor-floor coupling). In our study, we


minimized the environmental noises and hardware variations by inspecting the surroundings and selecting sensors with consistent signals during preliminary tests on pure noise data. However,


floor heterogeneity is unavoidable as it is determined by the user’s site. Therefore, we include the sensor number in the step-level features to assist the hierarchical model in recognizing


the data distribution shifts across various sensors at the initial level of aggregation. This allows the model to automatically capture the correlation between the sensor and the data


during training. DISCUSSION ON THE VARIABILITY OF FLOORS, SHOES, AND PARTICIPANTS The floor vibration induced by human gait is not only influenced by gait patterns, but also by the floor


properties, shoe types, and the participants’ body configurations43. For example, existing studies have found that the difference in floor properties results in shifts in vibration frequency


ranges due to the changes in stiffness and mass of the floor material41,44. The method developed in these studies can be used to generalize the results in our study to more floor types. In


addition, our preliminary work on the shoe type effect has found changes in the frequency spectrum of individual footsteps (i.e., step level features), but it does not have a significant


effect on the estimation of the walking speed and symmetry in the trace level. Further studies on the shoe effect on initial contact type estimation are needed to enhance the robustness of


the method. Moreover, the participant’s body configurations also contribute to the resultant floor vibration, as discussed in previous studies45. The body effect (e.g., height, weight) has


been considered in this study through the development of person-level feature aggregation in our hierarchical model. BROADER IMPACTS OF AMBIENT FLOOR VIBRATION SENSING FOR GAIT ASSESSMENTS


The use of footstep-induced floor vibration sensing for gait analysis has potential broad impacts on the surveillance of other gait-related diseases, as well as promoting in-home physical


health monitoring. For instance, this technology can be used to assist with understanding the impact of disease progression and other treatments of more common neurodegenerative diseases


such as Parkinson’s and Alzheimer’s disease, which affect the gait patterns of individuals at an early stage. By continuously monitoring an individual’s gait patterns, healthcare


professionals can detect changes in gait, which indicate the progression of these diseases or the effects of a particular treatment. In addition, the technology can be used for monitoring


other conditions that affect gait, such as osteoarthritis and stroke. Such gait information will allow healthcare professionals to assess the severity of gait-related conditions in


finer-granularity and tailor treatment plans to the individual’s needs. Furthermore, this method offers a non-intrusive and low-cost approach to collecting gait features, which can be


particularly useful for long-term monitoring of individuals in their homes or elder care facilities. By detecting changes in gait patterns, healthcare professionals can also develop


interventions to mitigate fall risks and other adverse health outcomes in older adults. Further studies are encouraged to adapt the method developed in this study to in-home environments to


address the remaining challenges brought by complex physical environments and diverse individual needs. Overall, the use of ambient floor vibration sensing has the potential for ubiquitous


and accessible gait analysis and physical health monitoring, by bringing functional gait assessments to local clinics and individuals’ homes. METHODS EXPERIMENT DESIGN The design of the


experiment aimed to explore the ability of floor vibration sensing to estimate gait parameters, extract gait symptoms, and track the functional stages of MD. We hypothesized that the floor


vibration signals would be able to extract temporal and spatial gait parameters, detect gait symptoms related to MD, and produce reliable predictions of MD stages. Therefore, we designed a


2-phase experiment to test this hypothesis. The first phase was a controlled experiment with healthy subjects in a controlled laboratory setting where the performance was validated with


reliable ground truth from the VICON Motion Capture System. The second phase was a real-world experiment with both healthy participants and children with MD, which was conducted in a


corridor at a children’s hospital to provide convenience for the participants during their regular clinical visits. All participants have provided written informed consent and/or assent and


all experiments are conducted in accordance with the approved protocols under relevant guidelines and regulations of Stanford Institutional Review Board (IRB) and University of Michigan


Institutional Review Board (IRB) (with approved protocol number IRB-55372, Single IRB-67992, and HUM00209461) approved the study. The laboratory experiment was designed to evaluate the


feasibility of using floor vibration signals for gait parameter estimation and symptom characterization. Healthy adults (n = 10, 4 male and 6 female; age = 21–40 years; body mass = 47–80 kg;


height = 161–180 cm) completed 20 trials of natural walking and 3–10 trials of abnormal walking on a 7-m long platform (Fig. 1a left). The platform in our laboratory is made of laminated


wood, which was designed to approximate the typical flooring used at home and was manually constructed by connecting wooden slabs and supporting structures with bolted steel plates. Four


geophones were placed on the floor surface along the edge of the walkway with a sampling frequency of 500 Hz. The abnormal walking conditions were completed in the order of toe and midfoot


initial contact, asymmetry walking with one leg wearing an ankle brace, and slow walking. The experiment was stopped when the number of trials reached 10 or when the subject requested a


rest. Ground truth records were collected with 10 VICON Motion Capture cameras with a sampling frequency of 100 Hz. The geophones were connected with the VICON Locker Lab to enable


synchronization21. 16 markers were used according to the marker placement specified by the VICON Plug-in Gait lower body model24. The VICON data were processed through a built-in pipeline to


crop the trials, fill in the missing values, and smooth the moving trajectories of each marker. The foot strike and foot off time were manually marked by an expert based on the


reconstructed foot contact and foot off trajectories. The gait parameters were computed through the Plug-in Gait model24, serving as the ground truth for evaluation. The field experiments


include two sensor layouts (Fig. 1a right). In the first experiment layout, patients with MD (n = 7, 4 male and 3 female; age = 7–15 years; body mass = 16–54 kg; height = 102–163 cm) and


healthy subjects (n = 6, 4 male and 2 female; age = 7–15 years; body mass = 41–85 kg; height = 143–183 cm) each completed 5–10 natural gait trials per person along a 15-m hospital corridor.


In the second experiment layout, patients with MD (n = 8, 7 male and 1 female; age = 7–15 years; body mass = 17–51 kg; height = 106–161 cm) and healthy subjects (n = 5, 3 male and 2 female;


age = 13–27 years; body mass = 35–88 kg; height = 125–182 cm) each completed 5–10 natural trials per person along a 10-m hospital corridor. The hospital corridor is made of concrete with


vinyl tiles on the surface, which is one of the most popular floor types for indoor living spaces. For both experiments, each trial was stopped when the number of trials reached 10 or when


the subject requested a rest. 5–8 geophones were placed on the floor surface along the edge of the walkway with a sampling frequency of 25600 Hz to maximize the temporal resolution. 3 and 5


video cameras were mounted at various locations along the corridor (Fig. 1a), aiming at the lower body of the walking subjects to collect the ground truth of gait symptoms. A hammer strike


was conducted at the beginning of each trial to enable synchronization of the video and vibration data. The video data were processed through manual cropping, MD symptom observation by an MD


specialist, and footstep counting for each trial. Ground truth of functional assessments on MD progression was obtained by medical practitioners from the children’s hospital, which include


the time to run 100 m, North Star Ambulatory Assessment (NSAA), and North Star Assessment for limb-girdle type muscular Dystrophy (NSAD)46. DEVELOPMENT OF A UNIFIED FUNCTIONAL SCALE FOR


PATIENTS WITH MD A unified scale for MD progression was defined based on the 100-m run time measured during the functional assessments conducted in clinics. Running speed is a simple,


well-established means to grossly quantify ambulation abilities47,48. The 100-m timed tests were recently introduced for use in individuals with neuromuscular disorders such as DMD and LGMD


as it is a simple-to-understand concrete disease that can be used in adults and children20,49. A unified scale to monitor their progression is needed because the purpose of developing the


floor vibration sensing approach is to advance the accessibility of gait assessments for general patients with various MD types. The scale was defined by dividing the performance based on


the normative time of a 100-m run defined in the previous study20. The normative 100-m run time was computed by comparing the actual time with the 50th percentile time among the healthy


controls, normalized by age, height, and weight: $$\begin{aligned} \quad Predicted \quad 100m\% = \frac{36.72 - 1.51 \times age (year)+ 0.26 \times \frac{weight (kg)}{height


(m^2)}}{Actual\quad 100m\quad Time} \times 100\% \end{aligned}$$ (1) where the predicted 100m % is the normative value ranges from 0% to 100%. The numerator is a running speed prediction


mode developed through a regression analysis20. A 100% value means an individual’s running time is the mean of the corresponding age group. The continuous value of predicted 100m % was


further discretized into several divisions, forming a reference of MD progression stage ranges from 0 to 7: MD stage Predicted 100 m% Interpretation Stage 0 100 Faster than 50th percentile


of the control subjects. Stage 1 80–99 Slower than 50th percentile of the control subjects. Could be early signs of functional decline. Stage 2 60–79 Prone to walk slightly slower and may


have flatfoot/toe contact. Stage 3 50–59 Prone to walk slower. Likely to have gait abnormalities such as shorter stride length and a wider base of support. Stage 4 40–49 May have noticeably


adapted gait patterns and may use wheelchairs part of the time. Stage 5 30–39 Likely to use wheelchairs for part of the day. Stage 6 20–29 Difficulty walking outside of their homes. About to


lose walking ability in several years. Stage 7 0–19 Likely to lose walking ability. VIBRATION DATA PROCESSING The floor vibration data were processed through an algorithmic pipeline where


footstep-induced signal impulses were detected and filtered. To detect the footstep-induced impulses in the ambient floor vibration, a peak detection algorithm was developed, which takes a


section of pure noise signal as a reference and applies a 0.1-s sliding window over the streaming data to identify the peaks in the vibration signals by comparing the data with that of the


pure noise. Impulse peaks with a mean amplitude more than three standard deviations above the noise mean were detected. Then, the duration between the impulses and the number of consecutive


impulses were extracted to determine whether they were induced by footsteps or not. Since footstep-induced signal impulses have a typical duration between 0.2 and 0.6 s, longer or shorter


signals were first excluded. Unlike impulses induced by door closing or item dropping, footstep-induced signals typically have more than three consecutive peaks as the person passes by.


Therefore, signals with less than three consecutive impulses were also excluded from the dataset. After detecting and isolating the footstep-induced vibration signals from the ambient floor


vibration, the signals were then filtered by a lowpass filter and Wiener filter to reduce noises. The lowpass filter aims to reduce the high-frequency sensory noises and exclude the


information that is not relevant to gait. A 500 Hz threshold was chosen because 97% of the signal power was included in the 0–250 Hz frequency range. The Wiener filter was used to reduce the


environmental noises by subtracting the spectrum of pure noise from that of the footstep-induced vibration signal. The processed vibration signals were stored on an encrypted cloud drive


where each sample describes an individual trace that consists of a series of consecutive footsteps from a person, recorded by one sensor. Before feature extraction and data modeling, the


samples were processed through a re-sampling algorithm to balance the sample number among various subjects for better generalization. This resampling algorithm integrates bootstrapping and


down-sampling, where the median sample size serves as a benchmark for adjusting the sample sizes of other subjects accordingly. This strategic adjustment improves the sample efficiency while


reducing redundancy within the dataset, aiming to improve the model performance. PHYSICS-INFORMED GAIT PATTERN EXTRACTION FROM FLOOR VIBRATION SIGNALS Floor vibrations generated by footstep


forces contain rich information about the gait and the floor. Similar to hammer strikes, each footstep can be regarded as a short-duration force applied to the floor, causing a small


deformation in the underlying floor slab. While the displacement is difficult to observe by the human eyes, it changes the internal stress distribution of the slabs, resulting in dynamic


floor movements to retain equilibrium. As the ensuing vibration response waves propagate through the floor, they can be measured by vibration sensors attached to the floor surface similar to


how seismologists measure earthquakes. The geophone sensors transform the vertical displacements of the floor into electrical voltage time series. If there is a slight change in the


footstep force or foot-floor contact surface due to gait symptoms related to MD, the floor vibration response changes accordingly, as described in an existing study using floor vibration


sensing13. Therefore, we leverage such changes to infer physical characteristics of gait patterns from individuals with MD. STEP TIME AND CADENCE ESTIMATION. The method to extract step time


and cadence from floor vibrations leverages the empirical observation that each footstep induces only one vibration impulse at the time when the foot strikes the floor. Therefore, we extract


the start time of the impulse to represent the foot strike time and count the number of impulse peaks within each trace to estimate the cadence. The specific process involves four steps.


First, we apply a wavelet transform using the Morse wavelet (an efficient and commonly used wavelet type) to obtain the time-frequency relationship in the vibration signals. Then, we isolate


the frequency range where the natural frequency of the floor lies (typically 5–25 Hz41,44) to filter out noises caused by mechanical device disturbances from the environment. The wavelet


coefficient series is then processed through an anomaly detection and peak-picking algorithm to extract the foot strike time and the number of footsteps. Finally, we compute the step time by


subtracting the foot strike time between adjacent steps, and the cadence through a division of the number of footsteps by the duration of the trace. $$\begin{aligned} Step\quad Time_i=


& {} t_{footstrike}^{i+1} - t_{footstrike}^{i}, \forall i=1,2,...,N \end{aligned}$$ (2) $$\begin{aligned} Cadence= & {} \frac{N-1}{t_{footstrike}^{N} - t_{footstrike}^{1}}


\end{aligned}$$ (3) where _N_ is the number of footsteps in a recorded trace. SYMMETRY SCORE ESTIMATION. The approach to extract the symmetry score is developed based on the insight that a


larger footstep force typically induces a higher amplitude in floor vibration at the same location. Since the two adjacent footsteps have relatively closer locations than the other footsteps


along the walking path, we assume that the wave attenuation effect is less dominant than the effect of the footstep force differences for the two adjacent steps. Therefore, we extract the


symmetry score based on the 90th percentile of the signal amplitude of each footstep and take the mean score among the trace to reduce the wave attenuation effect for different left–right


pairs. The 90th percentile instead of the maximum value to minimize the estimation bias caused by signal clipping or extreme values due to noises. The symmetry score is estimated as follows:


$$\begin{aligned} Symmetry \quad Score = 1 - \frac{1}{N-1} \sum _{i=1}^{N-1} \frac{|X_{90}^{i+1} - X_{90}^{i}|}{0.5(X_{90}^{i+1} + X_{90}^{i})} \end{aligned}$$ (4) where \(X_{90}^{i}\) is


the 90th percentile of the signal amplitude for \(i^{th}\) footstep and _N_ is the number of footsteps in a trace. The higher the value is, the more symmetrical a person’s gait is. INITIAL


CONTACT PREDICTION. To examine how various initial contacts affect the resultant floor vibration, we formulate the dynamical system of foot-floor contact to extract features that are


representative of initial contact types. We assume that each footstep exerts a force \(F_l(t)\) at a simply supported beam within the linear elastic range to simplify the complex


situation50. The equation of motion suggests: $$\begin{aligned} M\ddot{u}(t) + C{\dot{u}}(t) + Ku(t) = F_l(t) = -S(t)\ddot{u}_f(t) \end{aligned}$$ (5) where _M_, _C_, _K_ are the mass,


damping, and stiffness matrix of the floor. \(F_l\) is the footstep force, which can be further expressed by the equivalent spatial loading matrix _S_(_t_) and the foot acceleration


\(\ddot{u}_f(t)\). In order to simplify the complex temporal and spatial dependency in the above equation, we focus on the instant time when the initial contact happens and assume


independence between temporal and spatial variables (i.e., \(S(t) = S\)). The above derivation suggests that the floor vibration signal is determined by the spatial distribution of the


footstep force and the amplitude and direction during the contact. This formulation validates the hypothesis from a theoretical perspective that we can still infer the characteristics of


initial contacts from the frequency components of floor vibration signals, without knowing the exact properties of the floor. Therefore, we infer the probability of toe contact by training a


data-driven model based on the frequency spectrum of the vibration signals from each footstep. The data-driven model leverages the support vector machine with a quadratic kernel to capture


the inter-dependency between various frequency ranges. The output of the data-driven model is the type of contact. In our model, we translate the confidence score of the prediction into the


probability of toe contact as the initial contact feature. HIERARCHICAL FEATURE MODELING THROUGH MULTI-LAYER NEURAL NETWORKS The developed hierarchical model involves three multi-layer


neural networks to aggregate the features. Since the feature dimension and sample size decrease as they are aggregated through the hierarchy, the scale of the model also decreases. This is


because a balanced ratio between the sample number and feature dimensions enables efficient learning and can effectively mitigate problems such as over-fitting. In this study, the first


neural network has three layers, each with 12 (input dimension), and 256, 64 neurons. The second neural network has three layers, with 20 (input dimension), 128, and 32 neurons. The third


neural network has two layers with 9 (input dimension) and 64 neurons. The third neural network can also be replaced by a simpler model architecture, such as k-nearest neighbor classifiers,


decision trees, and support vector machine classifiers because the feature embeddings are already distinguishable among different classes as observed in Figure 4c. The operations in


\(l^{th}\) layer includes a linear transformation \(h_l\) and an activation \(a_l\): $$\begin{aligned} h_l= & {} w^T_l x + b_l \end{aligned}$$ (6) $$\begin{aligned} a_l= & {}


ReLu(h_l) = max(0, h_l) \end{aligned}$$ (7) where \(w_l, b_l\) are model parameters. We choose the commonly used “ReLu” activation because it introduces non-linearity to a neural network and


solves the vanishing gradients issue, which has been shown to enable the model to learn faster and perform better51. The output from the last layer in each hierarchy is then aggregated by


computing the mean value and then concatenated with the features in the next hierarchy. For example, all footsteps in the same trace were aggregated by computing the mean among all of them


and then concatenated with the trace-level features. Specifically, if the \(j^{th}\) trace has a set of footsteps \(T_j\), then input to the trace-level neural network is the concatenation


of trace-level features and step-level aggregations: $$\begin{aligned} h_j = concat(h_j^{trace},h_j^{steps}) \end{aligned}$$ (8) where $$\begin{aligned} h_j^{steps} = Mean(h_i, i \in T_j)


\end{aligned}$$ (9) The hierarchical neural network is trained hierarchically in two steps. First, the neural network at each hierarchy is pre-trained with labels before aggregation with a


cross-entropy loss commonly used for classification tasks. This allows “teacher enforcing”, which means each neural network can effectively learn the features related to MD progression.


Compared to the architecture where the labels are only applied at the final hierarchy, the “teacher enforcing” step enables more efficient learning with less variance and error propagation.


After that, the entire model is trained together to allow information sharing among multiple hierarchies. A softmax function52 was used to normalize the embedding from the previous hierarchy


before it was concatenated with the normalized features in the next hierarchy. In addition, a 20% dropout was applied to the model to mitigate overfitting, where the rate is determined


through empirical tests among various dropout percentages to optimize the test performance. The final output is a vector representing the probability of a person’s footsteps belonging to


each progression stage. The progression stage with the highest probability was determined as the final prediction. EVALUATION METRICS The evaluation metrics in this study are the mean


absolute error for estimating continuous values of gait parameters, and the F-1 score to evaluate and compare the performance of classification. F-1 SCORE. The F1 score is a measure of a


model’s accuracy on a dataset. It is commonly used to evaluate classification systems when the samples in each class are imbalanced. Since the MD stages among our test subjects are


imbalanced, the F1 score is chosen to balance between false negatives and false positives53. The F1 score is the harmonic mean of precision and recall, and thus symmetrically represents both


in one metric. The precision and recall are computed based on the number of true positives (TP), false positives (FP), and false negatives (FN) for each class. For a multi-class


classification problem in our study, we calculate the average of F-1 scores among all classes. For each class, the F-1 score is computed as follows: $$\begin{aligned} F-1 \quad Score =


\frac{2\times Precision \times Recall}{Precision + Recall} \end{aligned}$$ (10) where $$\begin{aligned} Precision = \frac{TP}{TP + FP}, \quad Recall = \frac{TP}{TP + FN} \end{aligned}$$ (11)


The F-1 score ranges from 0 to 1. A higher F-1 score typically means better prediction accuracy. In this study, the mean F-1 score is used to evaluate the performance of initial contact and


symmetry prediction, as well as the estimation of MD stages. MEAN ABSOLUTE ERROR. The mean absolute error (MAE) is a frequently used measure of the differences between values predicted by a


model and the ground truth values. Given _N_ observations, let the prediction and ground truth for each data point be \(\hat{x_i}\) and \(x_i\), the MAE is defined as follows:


$$\begin{aligned} MAE = \frac{\sum _{i=1}^{N} |x_i - \hat{x_i}|}{N} \end{aligned}$$ (12) MAE is the standard deviation of the residuals, which describes how far the predicted value is from


the true data points. MAE is a direct measure of the mean of these residuals: a smaller value means a more consistent match between the prediction and the ground truth. Since MAE has the


same unit as the original variable, it provides an intuitive comparison between the prediction and the ground truth, which is more effective in capturing the overall model performance than


the root-mean-square error (RMSE) metric54. Therefore, we choose MAE to estimate the accuracy of step time and cadence estimation. DATA AVAILABILITY Sample datasets of the healthy subjects


from all three studies are made publicly available at https://zenodo.org/record/8125744. The use of patients’ data and personal biometric information in further scientific work will require


a data-sharing agreement with the hospital. CODE AVAILABILITY Data processing and feature extraction were performed using custom Matlab scripts. The model was implemented as custom scripts


in both Python and Matlab. All codes are made publicly available along with the dataset at https://zenodo.org/record/8125744. REFERENCES * Bushby, K. _et al._ Diagnosis and management of


Duchenne muscular dystrophy, part 1: Diagnosis, and pharmacological and psychosocial management. _Lancet Neurol._ 9(1), 77–93 (2010). Article  PubMed  Google Scholar  * Parsons, E. P.,


Clarke, A. J. & Bradley, D. M. Developmental progress in Duchenne muscular dystrophy: Lessons for earlier detection. _Eur. J. Paediatr. Neurol._ 8(3), 145–153 (2004). Article  PubMed 


Google Scholar  * Amoasii, L. _et al._ Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy. _Sci. Transl. Med._ 9(418), 756–760 (2017).


Article  Google Scholar  * Landfeldt, E. _et al._ Life expectancy at birth in Duchenne muscular dystrophy: A systematic review and meta-analysis. _Eur. J. Epidemiol._ 35, 643–653 (2020).


Article  PubMed  PubMed Central  Google Scholar  * Yiu, E. M. & Kornberg, A. J. Duchenne muscular dystrophy. _J. Paediatr. Child Health_ 51(8), 759–764 (2015). Article  PubMed  Google


Scholar  * Bushby, K. _et al._ Diagnosis and management of Duchenne muscular dystrophy, part 1: Diagnosis, and pharmacological and psychosocial management. _Lancet Neurol._ 9(1), 77–93


(2010). Article  PubMed  Google Scholar  * Angelini, C. The role of corticosteroids in muscular dystrophy: A critical appraisal. _Muscle Nerve Off. J. Am. Assoc. Electrodiagn. Med._ 36(4),


424–435 (2007). Article  CAS  Google Scholar  * McDonald, C. M. _et al._ The 6-minute walk test as a new outcome measure in Duchenne muscular dystrophy. _Muscle Nerve_ 41(4), 500–510 (2010).


Article  PubMed  Google Scholar  * D’Angelo, M. G. _et al._ Gait pattern in Duchenne muscular dystrophy. _Gait Posture_ 29(1), 36–41 (2009). Article  PubMed  Google Scholar  * Abinaya, B.,


Latha, V. & Suchetha, M. An advanced gait monitoring system based on air pressure sensor embedded in a shoe. _Procedia Eng._ 38(3), 1634–1643 (2012). Article  Google Scholar  * Lin, F.,


Wang, A., Zhuang, Y., Tomita, M. R. & Wenyao, X. Smart insole: A wearable sensor device for unobtrusive gait monitoring in daily life. _IEEE Trans. Ind. Inf._ 12(6), 2281–2291 (2016).


Article  Google Scholar  * de Carvalho, E. V., Hukuda, M. E., Escorcio, R., Voos, M. C. & Caromano, F. A. Development and reliability of the functional evaluation scale for Duchenne


muscular dystrophy, gait domain: A pilot study. _Physiother. Res. Int._ 20(3), 135–146 (2015). Article  PubMed  Google Scholar  * Dong, Y., Zou, J. J., Liu, J., Fagert, J., Mirshekari, M.,


Lowes, L., Iammarino, M., Zhang, P. & Noh, H. Y. Md-vibe: physics-informed analysis of patient-induced structural vibration data for monitoring gait health in individuals with muscular


dystrophy. In _Adjunct proceedings of the 2020 ACM international joint conference on pervasive and ubiquitous computing and proceedings of the 2020 ACM international symposium on wearable


computers_, 525–531 (2020). * Van Iersel, M. B. & Mulley, G. P. What is a waddling gait?. _Disabil. Rehabil._ 26(11), 678–682 (2004). Article  PubMed  Google Scholar  * National Library


of Medicine. Waddling gait, https://www.ncbi.nlm.nih.gov/medgen/66667 (2024). * Pan, S., Wang, N., Qian, Y., Velibeyoglu, I., Noh, H. Y. & Zhang, P. Indoor person identification through


footstep induced structural vibration. _HotMobile 2015 - 16th International Workshop on Mobile Computing Systems and Applications_, 81–86 (2015). * Karg, M., Kühnlenz, K. & Buss, M.


Recognition of affect based on gait patterns. _IEEE Trans. Syst. Man Cybern. Part B (Cybernet.)_ 40(4), 1050–1061 (2010). Article  Google Scholar  * Michalak, J., Burg, J. & Heidenreich,


T. Don’t forget your body: Mindfulness, embodiment, and the treatment of depression. _Mindfulness_ 3, 190–199 (2012). Article  Google Scholar  * Dodge, H. H., Mattek, N. C., Austin, D.,


Hayes, T. L. & Kaye, J. A. In-home walking speeds and variability trajectories associated with mild cognitive impairment. _Neurology_ 78(24), 1946–1952 (2012). Article  CAS  PubMed 


PubMed Central  Google Scholar  * Alfano, L. N. _et al._ The 100-meter timed test: Normative data in healthy males and comparative pilot outcome data for use in duchenne muscular dystrophy


clinical trials. _Neuromuscul. Disord._ 27(5), 452–457 (2017). Article  PubMed  Google Scholar  * Vicon motion capture system. * Merriaux, P., Dupuis, Y., Boutteau, R., Vasseur, P. &


Savatier, X. A study of vicon system positioning performance. _Sensors_ 17(7), 1591 (2017). Article  ADS  PubMed  PubMed Central  Google Scholar  * Windolf, M., Götzen, N. & Morlock, M.


Systematic accuracy and precision analysis of video motion capturing systems-exemplified on the vicon-460 system. _J. Biomech._ 41(12), 2776–2780 (2008). Article  PubMed  Google Scholar  *


Vicon plug-in gait lower-body model. * Fagert, J., Mirshekari, M., Zhang, P. & Noh, H. Y. Recursive sparse representation for identifying multiple concurrent occupants using floor


vibration sensing. _Proc. ACM Interact. Mob. Wearable Ubiquitous Technol._ 6(1), 1–33 (2022). Article  Google Scholar  * Doglio, L. _et al._ Early signs of gait deviation in Duchenne


muscular dystrophy. _Eur. J. Phys. Rehabil. Med._ 47(4), 587–94 (2011). CAS  PubMed  Google Scholar  * Osoba, M. Y., Rao, A. K., Agrawal, S. K. & Lalwani, A. K. Balance and gait in the


elderly: A contemporary review. _Laryngoscope Investig. Otolaryngol._ 4(1), 143–153 (2019). Article  PubMed  PubMed Central  Google Scholar  * Katz-Leurer, M., Rotem, H., Lewitus, H., Keren,


O. & Meyer, S. Relationship between balance abilities and gait characteristics in children with post-traumatic brain injury. _Brain Inj._ 22(2), 153–159 (2008). Article  PubMed  Google


Scholar  * Heckmatt, J. Z. _et al._ Prolongation of walking in Duchenne muscular dystrophy with lightweight orthoses; Review of 57 cases. _Dev. Med. Child Neurol._ 27(2), 149–154 (1985).


Article  CAS  PubMed  Google Scholar  * Cornelio, F. _et al._ Functional evaluation of Duchenne muscular dystrophy: Proposal for a protocol. _Ital. J. Neurol. Sci._ 3, 323–330 (1982).


Article  CAS  PubMed  Google Scholar  * Pan, S., Ramirez, C. G., Mirshekari, M., Fagert, J., Chung, A. J, Hu, C. C., Shen, J. P., Noh, H. Y. & Zhang, P. Surfacevibe: Vibration-based tap


& swipe tracking on ubiquitous surfaces. In _Proceedings of the 16th ACM/IEEE International Conference on Information Processing in Sensor Networks_, 197–208 (2017). * Sutherland, D. H.


_et al._ The pathomechanics of gait in Duchenne muscular dystrophy. _Dev. Med. Child Neurol._ 23(1), 3–22 (1981). Article  CAS  PubMed  Google Scholar  * Sienko Thomas, S. _et al._


Classification of the gait patterns of boys with Duchenne muscular dystrophy and their relationship to function. _J. Child Neurol._ 25(9), 1103–1109 (2010). Article  PubMed  Google Scholar 


* MCDonald, C. M. _et al._ The 6-minute walk test in Duchenne/Becker muscular dystrophy: Longitudinal observations. _Muscle Nerve_ 42(6), 966–974 (2010). Article  PubMed  Google Scholar  *


D’Angelo, M. G. _et al._ Gait pattern in Duchenne muscular dystrophy. _Gait Posture_ 29(1), 36–41 (2009). Article  PubMed  Google Scholar  * Ruzbarsky, J. J., Scher, D. & Dodwell, E. Toe


walking: Causes, epidemiology, assessment, and treatment. _Curr. Opin. Pediatr._ 28(1), 40–46 (2016). Article  PubMed  Google Scholar  * Hsu, J. D. & Furumasu, J. Gait and posture


changes in the Duchenne muscular dystrophy child. _Clin. Orthop. Relat. Res._ 1976–2007(288), 122–125 (1993). Google Scholar  * Rijken, N. H. M. _et al._ Skeletal muscle imaging in


facioscapulohumeral muscular dystrophy, pattern and asymmetry of individual muscle involvement. _Neuromuscul. Disord._ 24(12), 1087–1096 (2014). Article  CAS  PubMed  Google Scholar  * Song,


T.-J., Lee, K.-A., Kang, S.-W., Cho, H. & Choi, Y.-C. Three cases of manifesting female carriers in patients with Duchenne muscular dystrophy. _Yonsei Med. J._ 52(1), 192–195 (2011).


Article  PubMed  Google Scholar  * Thompson, R. & Straub, V. Limb-girdle muscular dystrophies-international collaborations for translational research. _Nat. Rev. Neurol._ 12(5), 294–309


(2016). Article  CAS  PubMed  Google Scholar  * Dong, Y. & Noh, H. Y. Structure-agnostic gait cycle segmentation for in-home gait health monitoring through footstep-induced structural


vibrations. * Dong, Y., Liu, J. & Noh, H. Y. Gaitvibe+: Enhancing structural vibration-based footstep localization using temporary cameras for in-home gait analysis. In _Proceedings of


the 20th ACM Conference on Embedded Networked Sensor Systems_, SenSys ’22, 1168-1174 (Association for Computing Machinery, New York, NY, USA, 2023). * Dong, Y., Fagert, J. & Noh, H. Y.


Characterizing the variability of footstep-induced structural vibrations for open-world person identification. _Mech. Syst. Signal Process._ 204, 110756 (2023). Article  Google Scholar  *


Dong, Y., Zhu, J. & Noh, H. Y. Re-vibe: vibration-based indoor person re-identification through cross-structure optimal transport. In _Proceedings of the 9th ACM International Conference


on Systems for Energy-Efficient Buildings, Cities, and Transportation_, 348–352 (2022). * Pan, S. _et al._ FootprintID: Indoor pedestrian identification through ambient structural vibration


sensing. _Proc. ACM Interact. Mob. Wearable Ubiquitous Technol._ 1(3), 1–31 (2017). Article  Google Scholar  * Miller, N. F. _et al._ Natural history of steroid-treated young boys with


Duchenne muscular dystrophy using the NSAA, 100 m, and timed functional tests. _Pediatr. Neurol._ 113, 15–20 (2020). Article  PubMed  Google Scholar  * Bohannon, R. W. Reference values for


the timed up and go test: A descriptive meta-analysis. _J. Geriatr. Phys. Ther_ 29(2), 64–68 (2006). Article  PubMed  Google Scholar  * Petian-Alonso, D. C., de Castro, A. C., de Queiroz


Davoli, G. B., Martinez, E. Z. & Mattiello-Sverzut, A. C. Defining ambulation status in patients with Duchenne muscular dystrophy using the 10-metre walk test and the motor function


measure scale. _Disabil. Rehabil._ 45(18), 2984–2988 (2023). Article  PubMed  Google Scholar  * James, M. K. _et al._ Validation of the north star assessment for limb-girdle type muscular


dystrophies. _Phys. Ther._ 102(10), pzac113 (2022). Article  PubMed  PubMed Central  Google Scholar  * Racic, V., Pavic, A. & Brownjohn, J. M. W. Experimental identification and


analytical modelling of human walking forces: Literature review. _J. Sound Vib._ 326(1–2), 1–49 (2009). Article  ADS  Google Scholar  * Szandała, T. Review and comparison of commonly used


activation functions for deep neural networks. In _Bio-inspired Neurocomputing._ 203–224 (2021). Chapter  Google Scholar  * Liu, W., Wen, Y., Yu, Z. & Yang, M. Large-margin softmax loss


for convolutional neural networks, _arXiv preprint_arXiv:1612.02295 (2016). * Goutte, C. & Gaussier, E. A probabilistic interpretation of precision, recall and f-score, with implication


for evaluation. In _Advances in Information Retrieval: 27th European Conference on IR Research, ECIR 2005, Santiago de Compostela, Spain, March 21-23, 2005. Proceedings 27_, 345–359


(Springer, 2005). * Willmott, C. J. & Matsuura, K. Advantages of the mean absolute error (MAE) over the root mean square error (RMSE) in assessing average model performance. _Clim. Res._


30(1), 79–82 (2005). Article  Google Scholar  Download references AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Stanford University, Stanford, USA Yiwen Dong, Jingxiao Liu, Mostafa


Mirshekari & Hae Young Noh * Nationwide Children’s Hospital, Columbus, USA Megan Iammarino & Linda Lowes * University of Michigan, Ann Arbor, USA Jesse Codling & Pei Zhang *


Baldwin Wallace University, Berea, USA Jonathon Fagert Authors * Yiwen Dong View author publications You can also search for this author inPubMed Google Scholar * Megan Iammarino View author


publications You can also search for this author inPubMed Google Scholar * Jingxiao Liu View author publications You can also search for this author inPubMed Google Scholar * Jesse Codling


View author publications You can also search for this author inPubMed Google Scholar * Jonathon Fagert View author publications You can also search for this author inPubMed Google Scholar *


Mostafa Mirshekari View author publications You can also search for this author inPubMed Google Scholar * Linda Lowes View author publications You can also search for this author inPubMed 


Google Scholar * Pei Zhang View author publications You can also search for this author inPubMed Google Scholar * Hae Young Noh View author publications You can also search for this author


inPubMed Google Scholar CONTRIBUTIONS Y.D. wrote the main manuscript text and prepared all the figures. H.Y.N., M.I., and L.L. provided suggestions and edits to the manuscripts and figures.


Y.D., M.I., J.C., L.L., J.F., M.M., and P.Z. developed the hardware and conducted the experiments. Y.D. and J.L. conducted data analysis and developed the model. All authors reviewed the


manuscript. CORRESPONDING AUTHOR Correspondence to Yiwen Dong. ETHICS DECLARATIONS COMPETING INTERESTS The authors declare no competing interests. ADDITIONAL INFORMATION PUBLISHER'S


NOTE Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. RIGHTS AND PERMISSIONS OPEN ACCESS This article is licensed under


a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate


credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article


are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and


your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this


licence, visit http://creativecommons.org/licenses/by/4.0/. Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Dong, Y., Iammarino, M., Liu, J. _et al._ Ambient floor vibration


sensing advances the accessibility of functional gait assessments for children with muscular dystrophies. _Sci Rep_ 14, 10774 (2024). https://doi.org/10.1038/s41598-024-60034-5 Download


citation * Received: 09 August 2023 * Accepted: 18 April 2024 * Published: 11 May 2024 * DOI: https://doi.org/10.1038/s41598-024-60034-5 SHARE THIS ARTICLE Anyone you share the following


link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature


SharedIt content-sharing initiative


Trending News

Changes for NatWest customers with 'between £1 and £10,000' in their account | Chronicle Live

Changes for NatWest customers with 'between £1 and £10,000' in bank accountNatWest has confirmed that it will be making ...

Luxury tipi bar with its own pizza van re-opens at rustic northumberland estate

A STUNNING TIPI BAR AT THE HEART OF A BEAUTIFUL ESTATE IN NORTHUMBERLAND HAS RE-OPENED FOR SUMMER 2025 16:32, 26 May 202...

Paul mitchell leaves newcastle live - updates and reaction to shock decision

THE BIG QUESTION After Dan Ashworth and Paul Mitchell both leave the club without fans seeing any real fluidity between ...

Firefighters issue urgent warning to brits with tumble dryer or dishwasher

A WARNING HAS BEEN ISSUED TO RESIDENTS IN THE WAKE OF A FIRE 21:36, 26 May 2025Updated 21:41, 26 May 2025 UK households ...

Liverpool parade incident LIVE: Police press conference updates latest on horror crash - Chronicle Live

NewsLiverpool parade incident LIVE: Police press conference updates latest on horror crashEmergency services descended o...

Latests News

Ambient floor vibration sensing advances the accessibility of functional gait assessments for children with muscular dystrophies

ABSTRACT Muscular dystrophies (MD) are a group of genetic neuromuscular disorders that cause progressive weakness and lo...

$2m raised for second pittsburgh fisher house to be built on va pittsburgh healthcare system’s heinz campus | va pittsburgh health care | veterans aff

Pittsburgh , PA — Friends of the Pittsburgh Fisher House Crosses $2M threshold in Capital Campaign for a second Pittsbur...

San francisco mayor gavin newsom to speak at techcrunch disrupt tomorrow | techcrunch

San Francisco Mayor Gavin Newsom will be bringing himself, his hair and his smile to TechCrunch Disrupt tomorrow, Tuesda...

slide | designboom.com

* imprint * privacy policy * terms of use * cookies * copyright info * contribute * about us * contact us * newsletter *...

paths | designboom.com

DESIGNER'S OWN WORDS: I tried to design a modern door handle with a technical yet organic style. Its colored versio...

Top