Shotgun approaches to gait analysis: insights & limitations
© Kaptein et al.; licensee BioMed Central Ltd. 2014
Received: 14 April 2014
Accepted: 7 August 2014
Published: 12 August 2014
Identifying features for gait classification is a formidable problem. The number of candidate measures is legion. This calls for proper, objective criteria when ranking their relevance.
Following a shotgun approach we determined a plenitude of kinematic and physiological gait measures and ranked their relevance using conventional analysis of variance (ANOVA) supplemented by logistic and partial least squares (PLS) regressions. We illustrated this approach using data from two studies involving stroke patients, amputees, and healthy controls.
Only a handful of measures turned out significant in the ANOVAs. The logistic regressions, by contrast, revealed various measures that clearly discriminated between experimental groups and conditions. The PLS regression also identified several discriminating measures, but they did not always agree with those of the logistic regression.
Discussion & conclusion
Extracting a measure’s classification capacity cannot solely rely on its statistical validity but typically requires proper post-hoc analysis. However, choosing the latter inevitably introduces some arbitrariness, which may affect outcome in general. We hence advocate the use of generic expert systems, possibly based on machine-learning.
KeywordsGait Coordination dynamics Data analysis
The assessment of movement is developing rapidly as a result of recent advances in data acquisition. Multiple signals can be readily recorded for considerable time spans. Parallel progress in data analysis allows for a combined application of more conventional, multivariate statistics like principal or independent components and stability-related measures, e.g., standard deviation of relative phase, Lyapunov exponents, and Floquet multipliers [1–5]. In the study of human gait, this led to many important findings regarding, e.g., the coordinative stability and adaptability of walking in relation to speed, curved walking, age and various pathologies including stroke, Parkinson’s disease, cerebral palsy, pregnancy-related pelvic pain, amputations and low back pain [6–16]. Collectively, these studies have demonstrated the expediency of various ‘novel’ measures in characterizing gait dynamics and their surplus value relative to ‘traditional’ kinematic measures pertaining to more isolated features of walking.
Despite the progress in data acquisition and analysis, several limitations have come to the fore. For instance, there is culminating evidence that stride fluctuations in young, healthy humans are characterized by a power law-like behavior (i.e., long-term correlations) that tends to vanish with age  and pathology (e.g., [18, 19]). Although important as a general observation, the underlying measure (scaling exponent) proved not sufficiently specific to differentiate between gait-related pathologies. Likewise, the stability-related measures have been instrumental in revealing task- and patient-specific changes in gait dynamics, but, as it stands, it is not evident how these measures relate to gait stability in a biomechanical sense, to proneness to falls, and to the various variability measures (e.g., standard deviation and coefficient of variation of stride duration). These limitations can be seen as derivatives from what we view as a potential problem of current gait analysis, namely that often measures and qualifiers are used that are selected a priori without thorough (theoretical) considerations. When this is the case, a more generic, unbiased method to determine a measure’s relevance may be preferred.
We discuss this by following what might be considered a more objective approach: browse through a large set of possible measures and assess their relevance for discriminating gait patterns by evaluating them according to their information content. This approach is typically applied in order to pinpoint measures that are most defining in characterizing different types of gait. Such a task is laborious and time-consuming but can be left to the computer when employing proper statistical evaluation. Statistics has the potential to provide (more) objective criteria for feature selection. This is expected particularly useful in more exploratory studies where, as said, in-depth theoretical underpinnings are lacking.
Our main goal is to gain insight into the feasibility of such a shotgun approach for movement assessment. That is, our interest here is not in the specifics of experimental designs and outcomes but in assembling a plenitude of measures and evaluating their capacity for classifying gait. We illustrate this by using data of two previous studies, which provided profound insight into altered gait patterns in amputees and in stroke patients. We ‘blindly’ created a large set of candidate outcome measures and tested them with different statistical approaches. To anticipate, defining the relevance of measures and, by this, reducing the set of measures seems feasible on first sight. Not unexpected, however, results differed between studies and between statistical approaches. Such discrepancies already indicate that also shotgun approaches are confronted by challenges due to the inevitably arbitrary choices regarding variable selection and subsequent statistical evaluation.
To demonstrate the shotgun approach we used data from two experimental studies, referred to as study A and B, that involved stroke patients and amputees walking on a treadmill, respectively. In brief, the aim of study A was to investigate the effect of balance support on gait parameters in patients with stroke. Study B addressed the effect of gait speed and of a cognitive dual task on gait of persons with an amputation compared to healthy controls. Primary outcomes of studies A and B have been partly published in  and , respectively. Study A involved only a single population under three conditions calling for initial statistical assessments in terms of a one-way ANOVA, whereas study B involved two populations implying an initial two-way ANOVA with condition as the within factor and | for study B | group as the between factor. As said, these data merely serve to show benefits and pitfalls of shotgun approaches. For this reason we only provide a very concise outline of the experimental design and data acquisition. More details can be found in  and .
Study A - stroke patients
Eighteen patients with stroke participated in study A. Participants walked on a treadmill for five minutes in three different conditions. In the first condition they were not allowed to hold the handrail for support and walked at their corresponding preferred speed. In the second condition participants used the rail for support and walked at their, typically altered, preferred speed. In the third condition, participants still held onto the rail but walking speed was set to the preferred speed of the unsupported condition .
Vertical ground reaction forces were obtained using an instrumented treadmill equipped with a force plate. From the ground reaction forces we determined the center-of-pressure (COP) trajectories, C O P x and C O P y (mediolateral [ML] and anterior-posterior [AP] direction, respectively). Trunk accelerations a x , a y , and a z (ML-, AP-, and vertical direction, respectively) were measured using a tri-axial accelerometer that was mounted near the level of the third lumbar spine segment. In addition, respiration was assessed breath-by-breath using a pulmonary gas exchange system which measured ventilation rate (), oxygen uptake (), carbon dioxide production (), respiratory exchange ratio (RER), metabolic costs (Cmet) and heart rate (HR). Cmet was computed via the oxygen uptake normalized by bodyweight and walking speed . The data of four participants had to be discarded because of technical problems leaving 14 sets for subsequent analysis.
Study B - amputees
Study B involved in total 46 participants: 26 with a lower-limb amputation and 21 abled-bodied controls. Of the former group, 16 had a transtibial and 10 a transfemoral amputation . Participants walked on an instrumented treadmill at a comfortable walking speed for four minutes in two different conditions. The first one consisted solely of walking, whereas in the second condition participants performed while walking a cognitive task inducing the Stroop effect: Participants saw a color name printed in color while listening to a spoken color name which either matched or not matched the color of the printed word. Whenever spoken and depicted color disagreed, participants had to press a button. This task had previously been shown to elicit changes in postural control in lower limb amputees during quiet stance .
Similar to study A a treadmill with built-in force plate served to measure vertical ground reaction forces during walking. Off-line computation yielded C O P x and C O P y . Participants also wore a tri-axial accelerometer mounted near the level of the third lumbar spine segment. The corresponding a x -, a y -, and a z -signals were sampled at a rate of 100 Hz. Oxygen uptake was assessed breath-by-breath using open-circuit respirometry providing , , , RER, Cmet, BF, and HR. Furthermore, bilateral surface EMGs were recorded from the tibialis anterior (TA), gastrocnemius (G), vastus medialis (VM), semitendinosus (S), and the tensor fascia latae (TFL), from which the envelopes were estimated (after high-pass filtering at 140 Hz, followed by full-wave rectification using the Hilbert transform, and low-pass filtering at 2 Hz) [24, 25]. Data of several participants had to be discarded because of acquisition problems leaving sets of 19 controls and 19 persons with amputation for analysis.
select an epoch around every step moment (we used a temporal window of 40% of the mean stride duration, which was estimated via the dominant frequency in the spectral distribution);
align the selected epochs and average over step moments – this averaging yields a template;
determine per event the time lag at which the serial-lag cross-covariance between epoch and template is maximal and shift the event by that time lag;
repeat the entire procedure until convergence.
With the so-defined COP-events we estimated mean step width , mean stride length, mean stride duration, and their respective coefficients of variation (CV). For both force plate and EMG signals we further derived the mean value and variance of the template over time representing the average mean COP position over the aforementioned temporal window (for the EMG the average rectified value) as well as its mean deviation. Moreover, we determined the mean variance over events averaged over time as measure of the template’s consistency, i.e. the ‘regularity’ of walking and muscle activation. That is, for each data point of the template we calculated the variance using the corresponding points in all epochs, and all these variances were averaged. Regularity of signals wasalso assessed in terms of the corresponding sample entropy [29, 30] following the approach of Lake and co-workers  (parameter values: m=3 and r varying from 0.01 to 0.07). We computed the sample entropy of (Hilbert-)amplitude and (Hilbert-)phase of the force plate, EMG and accelerometer signal.
To address other complexity-related features we analyzed the signals’ temporal correlation structure using detrended fluctuation analysis (DFA) [32, 33]. DFA yields a parameter α (scaling index or self-similarity parameter) that equals the so-called Hurst exponent  under the assumption that the generating process represents fractal Gaussian noise: A fully random signal (white noise) corresponds to α=0.5; signals containing anti-persistent correlations have α<0.5, and persistent correlations imply α>0.5. Finally, we determined the maximum Lyapunov exponents as measure for (local, dynamic) gait stability [34–37]. We employed Rosenstein and co-workers’ algorithm with embedding dimension M=7 (estimated via the number of false nearest neighbors) and τ=20 samples embedding delay (estimated via the first minimum of the average mutual information) . Maximum Lyapunov exponents were determined for the EMG and acceleration signals as well as for their principal components. The latter were determined through conventional principal component analysis (PCA) , from which we also stored the corresponding eigenvalue spectrum for subsequent statistical assessment  (i.e. three and five eigenvalues for accelerometer and EMG signals, respectively).
The following measures entered our statistical assessments – we sorted measures by recording modality; where numbers in between parentheses indicate for how many dimensions, channels, or muscles a measure was determined (e.g., x, y, and z for accelerometer data and C O P x , C O P y , and F z for force plate data).
Ground reaction force: mean and CV of step width, stride length, and stride duration; DFA- α of stride duration, mean and CV of event position (3), DFA- α of event position (3), template mean (3), mean variance over events (3), sample entropy (3), standard error of sample entropy (3), sample entropy of phase (3), standard error of sample entropy of phase (3).
Accelerometry: max. Lyapunov exponent (3), sample entropy (3), standard error of sample entropy (3), PCA eigenvalues (3), max. Lyapunov exponent of principal components (3).
Metabolism: mean and CV of , , , RER, BF, Cmet, and HR; no breathing-frequency data were available for stroke patients, i.e. there we used only twelve metabolic measures.
EMG: median frequency (5), template mean (5), mean variance over events (5), sample entropy (5), standard error of sample entropy (5), max. Lyapunov exponent (5), PCA eigenvalues (5), max. Lyapunov exponents of PCA components (5), sample entropy of phase (5), standard error of sample entropy of phase (5).
The total number of distinct (though possibly correlated) measures was 61 for study A and 113 for study B.
As a first step, we tested main and interaction effects for all measures considered. We conducted separate repeated measures ANOVAs with condition as the within factor and–for study B–group as the between factor. To facilitate comparison of study A with study B we also performed supplementary analyses for study B by determining first the relative difference (i.e., the difference between the measures of the two conditions divided by their mean) that were entered into a one-way ANOVA as in study A. Because the aim of our shotgun approach was to “identify relevant measures in (changes of) gait patterns” we preferred individual ANOVAs over multivariate approaches (e.g., MANOVA, PCA) . Note that the very large number of measures typically incorporated in shotgun approaches renders MANOVAs in general less feasible.
Multinomial logistic regression
In order to determine which of the measures constitute the best predictors for an experimental factor (group or condition), we used nominal multinomial logistic regression models. In a nutshell, such models fit the log-probability that a nominal factor falls in a certain category, expressed as a fraction of the probability that it falls in another category, i.e. . In this expression π j denotes the probability that the factor of interest is in category j, k represents the reference category, x i are the values of the ith measurement, β ij are the regression coefficients, and n is the number of included measures. Since we incorporated three conditions in study A and three groups in study B, the regression initially returned two vectors of β-coefficients, namely β13 and β23 (number 3 is the reference group). However, the third coefficient β12 simply equals β13−β23. To estimate the overall importance of a measure, we finally determined the β-norm (i.e. ). Here it is important to realize that we considered more measures than observations. Therefore the number of measures in the regression had to be constrained. We selected measures using the corresponding p-values resulting from the individual ANOVAs; see Figure 2, left panel. We used either only the measures with p<0.05/N or sorted all measures by p-value in descending order and considered the first seven values onlya. All measures were normalized to z-scores before entering the regression. For study B we used the relative difference between the measures of the two conditions as input for the regression.
The overall performance of the regression was quantified in terms of the correct rate. For this, we first computed the β-coefficients. Next, we determined the predicted probabilities for each category and classified the observation according to the highest probability. Then, the correct rate was given by the fraction of observations classified properly. Note that it would have been more appropriate to divide the observations into a training and a test set, but the number of observations was not large enough to do so.
Partial least squares regression
Partial least squares (PLS) regression deals with correlated measures by decomposing in- and output into factor scores which are linearly independent. PLS is similar to principal component analysis (PCA) but PCA relies on the covariance between input variables, whereas PLS capitalizes on the covariance between the input and response variables. In brief, PLS decomposes the input X (n observations ×m measures) and the output Y (n observations ×k categories) into X=T P t +δ and Y=U Q t +ε, respectively. T and U are the score matrices (both n × l), P and Q are the loading matrices (n×m and k × l, respectively), δ and ε are residuals, and l denotes the number of components. Presuming a linear relation between T and U, these equations can be combined in the form Y≈Xβ, which is the searched-after linear model .
Since we included nominal variables (condition and group), we used an indicator matrix as the response variable . As in conventional PCA, we here limited the number of new components used in the regression, i.e. l ≪ m. In particular, we used seven components in the PLS regression in agreement with the aforementioned multinomial logistic regression1; cf. Results. Note that testing for significance of the PLS regression is possible but not straightforward . For the sake of brevity we here decided not to add such a test. Quantification of performance was realized in the same way as in the multinomial logistic regression, i.e. using the correct rate; see Figure 2.
Measures from the participants with stroke that show a significant condition effect
Measures from the participants with an amputation that showed a significant effect
Mean step width
Mean stride duration
CV of stride duration
0.0002 (0.66) 
Template mean (x)
0.0003 (0.34) 
Mean variance events (z)
SE of sample entropy (y)
SE of sample entropy (z)
Sample entropy of phase (z)
SE of sample entropy of phase (y)
Sample entropy (S)
Lyapunov exponent (G)
Sample entropy (x)
PCA eigenvalues (1)
< 0.00001 (0.96)
Multinomial logistic regression
β -coefficients of the logistic regression for study A, using the 7 measures with the highest p -value (2nd column)
Accelerometer lyapunov exponent (y)
Metabolism mean Cmet
Accelerometer lyapunov of PC (1)
Force plate DFA- α of stride duration
β -coefficients of the logistic regression for study B, using the relative difference between non-Stroop and Stroop results as measure
Force plate SE of sample entropy (y)
EMG sample entropy (TA)
Force plate DFA- α of stride duration
EMG SE of sample entropy of phase (VM)
Metabolism mean (HR)
EMG PCA eigenvalues (5)
Force plate mean template (z)
Regression coefficients of the PLS regression for study A
Force plate DFA- α of stride duration
Force plate DFA- α of event position (z)
Force plate mean template (z)
Force plate DFA- α of event position (y)
Metabolism cv of RER
Force plate SE of sample entropy (z)
Force plate mean event position (z)
Regression coefficients of the PLS regression for study B
Force plate SE of sample entropy (y)
Force plate DFA- α of stride duration
EMG SE of sample entropy (VM)
Force plate sample entropy (y)
Accelerometer sample entropy (z)
EMG PCA eigenvalues (5)
EMG SE of sample entropy of phase (VM)
EMG sample entropy (TA)
EMG PCA eigenvalues (1)
EMG SE of sample entropy of phase (S)
Shotgun approaches for analyzing multivariate gait signals can provide important insights into gait classification but they are also confronted with considerable challenges. We used data of two experimental studies to illustrate these challenges. Study A had a one-way design as the one patient group was tested in three conditions: walking unsupported at their preferred walking speed, supported at their preferred speed, and walking supported at their preferred speed of the unsupported condition. Study B incorporated three groups, two types of lower-limb amputees and a control group, that were assessed in two conditions (i.e. a two-way design). In both cases we determined large sets of outcome measures that underwent different statistical assessments; see Figure 2 for a schematic overview.
Conventional ANOVAs returned significant main effects for study A and B, in the absence of significant interaction effects for study B. In study A, three metabolic measures were found to be significant (c.f., ), in study B, stride length and metabolic costs revealed group effects (e.g., [43–45]). The absence of more main effects that could be expected based on the established literature might be explained by the correction for multiple comparisons. The Bonferroni correction that we used is the most common one, but it is also quite conservative. Of course, we could have chosen alternatives like the Šidák correction, or even could have followed an entirely different route, like the Benjamini-Hochberg procedure . However, this would not have helped to overcome the fundamental problem: A shotgun approach may involve such an arbitrarily large set of measures that conventional statistical assessments (e.g., ANOVAs) simply become unfeasible; just adding measures will inevitably suppress significance and, on top of that, measures may be correlated, which may hamper analysis too.
We followed alternative routes, albeit equally arbitrary, and employed a multinomial logistic as well as a partial least squares regression. For the logistic regression, we used the ANOVA results to limit the number of input measures, while we used all measures in the PLS regression. Both regressions performed well in terms of success rate, which varied from 77% to 100%, indicating that the regression weights are indicative of a measure’s relative classification capacity. The logistic regressions also returned multiple significant coefficients. Notably, the regressions for study B, targeted at examining the interaction effect, performed very well while no interaction effect was found in the ANOVA.
It may be difficult to find clear correlations between many of the chosen measures and complex gait patterns. The ‘insufficiency’ of the conventional ANOVAs and the ‘improved’ performance of the logistic and PLS regression in revealing the measures’ relationships with experimental groups and conditions may be self-evident. However, when comparing the results of the logistic regression with those of the PLS regression one can realize that the measures identified as relevant differ between approaches. For example, the mean ventilation rate has the highest weight in the logistic regression for study A (Table 3), but it does not appear at all in the results of the PLS regression (Table 5). For study A, only one measure appears in both regressions, namely the DFA- α of stride duration. For study B, the results are more similar, with 5 of the 7 measures appearing in both tables. Both statistical post-hoc assessments appear valid, at least from a more mathematical perspective, with the addition that PLS regression accounts for possible correlations between measures. We did expect results to differ but having said that the question remains: How can one decide which measures are appropriate? As the number of measures continues to increase, this question will become more important.
There are several more caveats to mention. For example, for study B we used the relative difference between the measures of the two conditions in the regression analysis. We could have chosen the ratio, the log-difference, or any other measure defining a proper metric. Similarly arbitrary was fixing the threshold to seven when ranking p-values in the logistic regression, or in fact choosing p-values for ranking instead of, for example, effect sizes. Moreover, the calculation of some of the outcome measures required making other arbitrary choices, such as the temporal window size in the event optimization procedure and the embedding parameters for the Lyapunov exponent, et cetera et cetera.
The logistic and PLS regressions are two selected additional methods to identify relevant measures. Statistics comes with a plethora of assessment methods from which most can be used in various (overlapping) circumstances. Our goal to stay as objective as possible is once more at stake because again we have to make somewhat arbitrary choices. That is, pushing the shotgun approach as far as possible by keeping it largely objective by including as little as possible a priori knowledge turned out to be quite challenging. While the feature definition progressed profoundly, the feature selection awaits to be implemented in a similarly advanced way. Especially in view of ‘big data’, i.e. the massive amount of data being collected to date, an apropriate feature selection is mandatory. One possibility for this would be to supplement the measure extraction by more generic, data-driven expert systems that capitalize on a priori data reduction [39, 47] – though here one simply pushes the selection problem back to the definition of measures. Alternatives are machine-learning techniques for pattern classification that are slowly penetrating gait analysis (e.g., [48–62]). We are currently developing a partly unsupervised learning approach that incorporates the literature-based educated guesses for measure selection. In future work we will compare this to the current study. In fact, all the here discussed signal-processing steps have already been implemented as an open-source toolbox .
We advocate to progress data analysis towards machine learning in combination with theory-based (i.e. educated) selection criteria. By the same token, however, we believe that shotgun approaches can be a valid addition when data-mining. As we illustrated in detail how post-hoc assessments may point at relevant measures and unravel interesting effects that may warrant further investigation. As it stands, however, proper insight into measure selection and post-hoc statistics remains mandatory.
Shotgun approaches can help identifying measures for gait assessment. This is particularly true if measures are incorporated that still lack a theoretical underpinning in the context of gait analysis. In order to extract a specific measure’s classification capacity, however, one cannot solely rely on its statistical validity (e.g., the outcome of an ANOVA). For the current examples we showed that both logistic as well as partial least squares regression produced interesting albeit diverging results. Both post-hoc analyses can be defended from a statistical/mathematical perspective. This difference is seminal for what we believe is a major concern: At some point in the analysis arbitrary choices are inevitable. While the outlined procedure may be useful in many situations, we believe that in order to create a blind approach, more generic methods are required. In this context one can think of machine-learning techniques or even more general expert systems borrowed from the field of artificial intelligence.
Written informed consent was obtained from all the participants for the publication of this report.
a Introducing a threshold always implies a degree of arbitrariness. Selecting p<0.05 to define significance is as arbitrary as selecting the seven largest p-values as done here. In fact we chose that cut-off at will because in the current study it only served to improve legibility, although there is a limit to the number of measures that can be included due to the finite sample size.
RK and AD received financial support from the Netherlands Organisation for Scientific Research (NWO grant #400-08-127).
- Dingwell J, Cusumano J, Sternad D, Cavanagh P: Slower speeds in patients with diabetic neuropathy lead to improved local dynamic stability of continuous overground walking. J Biomech. 2000, 33 (10): 1269-1277.View ArticlePubMedGoogle Scholar
- Dingwell JB, Kang HG: Differences between local and orbital dynamic stability during human walking. J Biomech Eng. 2007, 129 (4): 586-593.View ArticlePubMedGoogle Scholar
- Hausdorff JM: Gait variability: methods, modeling and meaning. J Neuroeng Rehabil. 2005, 2 (1): 19-View ArticlePubMedPubMed CentralGoogle Scholar
- Lamoth CJC, Beek PJ, Meijer OG: Pelvis–thorax coordination in the transverse plane during gait. Gait Posture. 2002, 16 (2): 101-114.View ArticlePubMedGoogle Scholar
- Yamasaki T, Nomura T, Sato S: Phase reset and dynamic stability during human gait. BioSystems. 2003, 71 (1): 221-232.View ArticlePubMedGoogle Scholar
- Courtine G, Schieppati M: Tuning of a basic coordination pattern constructs straight-ahead and curved walking in humans. J Neurophysiol. 2004, 91 (4): 1524-1535.View ArticlePubMedGoogle Scholar
- Desloovere K, Molenaers G, De Cat J, Pauwels P, Van Campenhout A, Ortibus E, Fabry G, De Cock P: Motor function following multilevel botulinum toxin type a treatment in children with cerebral palsy. Dev Med Child Neurol. 2007, 49 (1): 56-61.View ArticlePubMedGoogle Scholar
- Diedrich FJ, Warren WHJr: The dynamics of gait transitions: effects of grade and load. J Mot Behav. 1998, 30 (1): 60-78.View ArticlePubMedGoogle Scholar
- Donker SF, Beek PJ: Interlimb coordination in prosthetic walking: effects of asymmetry and walking velocity. Acta Psychologica. 2002, 110 (2): 265-288.View ArticlePubMedGoogle Scholar
- Haken H, Kelso JS, Fuchs A, Pandya AS: Dynamic pattern recognition of coordinated biological motion. Neural Netw. 1990, 3 (4): 395-401.View ArticleGoogle Scholar
- Kang HG, Dingwell JB: Effects of walking speed, strength and range of motion on gait stability in healthy older adults. J Biomech. 2008, 41 (14): 2899-2905.View ArticlePubMedGoogle Scholar
- Lamoth CJC, Daffertshofer A, Huys R, Beek PJ: Steady and transient coordination structures of walking and running. Hum Mov Sci. 2009, 28 (3): 371-386.View ArticlePubMedGoogle Scholar
- Lamoth CJC, Meijer OG, Daffertshofer A, Wuisman PIJM, Beek PJ: Effects of chronic low back pain on trunk coordination and back muscle activity during walking: changes in motor control. Eur Spine J. 2006, 15 (1): 23-40.View ArticlePubMedPubMed CentralGoogle Scholar
- Lamoth CJC, Ainsworth E, Polomski W, Houdijk H: Variability and stability analysis of walking of transfemoral amputees. Med Eng Phys. 2010, 32 (9): 1009-1014.View ArticlePubMedGoogle Scholar
- van Emmerik R, McDermott W, Haddad JM, van Wegen E: Age-related changes in upper body adaptation to walking speed in human locomotion. Gait Posture. 2005, 22 (3): 233-239.View ArticlePubMedGoogle Scholar
- Wu W, Meijer OG, Jutte PC, Uegaki K, Lamoth CJC: Sander de Wolf G, van Dieën JH, Wuisman PIJM, Kwakkel G, de Vries JIP, Beek PJ: Gait in patients with pregnancy-related pain in the pelvis: an emphasis on the coordination of transverse pelvic and thoracic rotations. Clin Biomech. 2002, 17 (9–10): 678-686.View ArticleGoogle Scholar
- Lipsitz LA, Goldberger AL: Loss of complexity and aging. JAMA. 1992, 267 (13): 1806-1809.View ArticlePubMedGoogle Scholar
- Hausdorff JM, Mitchell SL, Firtion R, Peng C, Cudkowicz ME, Wei JY, Goldberger AL: Altered fractal dynamics of gait: reduced stride-interval correlations with aging and huntington’s disease. J Appl Physiol. 1997, 82 (1): 262-269.PubMedGoogle Scholar
- Hausdorff JM: Gait dynamics in parkinson’s disease: common and distinct behavior among stride length, gait variability, and fractal-like scaling. Chaos: Interdiscip J Nonlinear Sci. 2009, 19 (2): 026113-026113.View ArticleGoogle Scholar
- IJmker T, Houdijk H, Lamoth CJ, Jarbandhan AV, Rijntjes D, Beek PJ, van der Woude LH: Effect of balance support on the energy cost of walking after stroke. Arch Phys Med Rehabil. 2013, 94 (11): 2255-2261.View ArticlePubMedGoogle Scholar
- Wezenberg D, van der Woude LH, Faber WX, de Haan A, Houdijk H: Relation between aerobic capacity and walking ability in older adults with a lower-limb amputation. Arch Phys Med Rehabil. 2013, 94 (9): 1714-1720.View ArticlePubMedGoogle Scholar
- Wezenberg D, de Haan A, van Bennekom C, Houdijk H: Mind your step: metabolic energy cost while walking an enforced gait pattern. Gait Posture. 2011, 33 (4): 544-549.View ArticlePubMedGoogle Scholar
- Geurts ACH, Mulder TW, Nienhuis B, Rijken R: Dual-task assessment of reorganization of postural control in persons with lower limb amputation. Arch Phys Med Rehabil. 1991, 72 (13): 1059-1064.PubMedGoogle Scholar
- Potvin JR, Brown SHM: Less is more: high pass filtering, to remove up to 99% of the surface emg signal power, improves emg-based biceps brachii muscle force estimates. J Electromyogr Kinesiol. 2004, 14 (3): 389-View ArticlePubMedGoogle Scholar
- Myers L, Lowery M, O’malley M, Vaughan C, Heneghan C, St Clair Gibson A, Harley Y, Sreenivasan R: Rectification and non-linear pre-processing of emg signals for cortico-muscular analysis. J Neurosci Methods. 2003, 124 (2): 157-165.View ArticlePubMedGoogle Scholar
- Plotnik M, Giladi N, Hausdorff JM: A new measure for quantifying the bilateral coordination of human gait: effects of aging and Parkinson’s disease. Exp Brain Res. 2007, 181 (4): 561-570.View ArticlePubMedGoogle Scholar
- Jordan K, Challis JH, Newell KM: Walking speed influences on gait cycle variability. Gait Posture. 2007, 26 (1): 128-134.View ArticlePubMedGoogle Scholar
- Roerdink M, Coolen BH, Clairbois BH, Lamoth CJC, Beek PJ: Online gait event detection using a large force platform embedded in a treadmill. J Biomech. 2008, 41 (12): 2628-2632.View ArticlePubMedGoogle Scholar
- Richman JS, Moorman JR: Physiological time-series analysis using approximate entropy and sample entropy. Am J Physiol Heart Circ Physiol. 2000, 278 (6): 2039-2049.Google Scholar
- Lamoth C, van Deudekom F, van Campen J, Appels B, de Vries O, Pijnappels M: Gait stability and variability measures show effects of impaired cognition and dual tasking in frail people. J Neuroeng Rehabil. 2011, 8 (1): 2-View ArticlePubMedPubMed CentralGoogle Scholar
- Lake DE, Richman JS, Griffin MP, Moorman JR: Sample entropy analysis of neonatal heart rate variability. Am J Physiol Regul Integr Comp Physiol. 2002, 283 (3): 789-797.View ArticleGoogle Scholar
- Peng CK, Mietus J, Hausdorff J, Havlin S, Stanley HE, Goldberger A: Long-range anticorrelations and non-gaussian behavior of the heartbeat. Phys Rev Lett. 1993, 70 (9): 1343-View ArticleGoogle Scholar
- Jordan K, Challis JH, Newell KM: Long range correlations in the stride interval of running. Gait Posture. 2006, 24 (1): 120-125.View ArticlePubMedGoogle Scholar
- Dingwell JB, Marin LC: Kinematic variability and local dynamic stability of upper body motions when walking at different speeds. J Biomech. 2006, 39 (3): 444-452.View ArticlePubMedGoogle Scholar
- Bruijn SM, Ten Kate WRT, Faber GS, Meijer OG, Beek PJ, van Dieën JH: Estimating dynamic gait stability using data from non-aligned inertial sensors. Ann Biomed Eng. 2010, 38: 2588-2593.View ArticlePubMedPubMed CentralGoogle Scholar
- Federolf P, Tecante K, Nigg B: A holistic approach to study the temporal variability in gait. J Biomech. 2012, 45 (7): 1127-1132.View ArticlePubMedGoogle Scholar
- Bruijn SM, Bregman DJJ, Meijer OG, Beek PJ, van Dieën JH: Maximum Lyapunov exponent as predictors of global gait stability: a modelling approach. Med Eng Phys. 2012, 34: 428-436.View ArticlePubMedGoogle Scholar
- Rosenstein MT, Collins JJ, De Luca CJ: A practical method for calculating largest Lyapunov exponents from small data sets. Phys Nonlinear Phenom. 1993, 65 (1–2): 117-134.View ArticleGoogle Scholar
- Daffertshofer A, Lamoth CJC, Meijer OG, Beek PJ: PCA in studying coordination and variability: a tutorial. Clin Biomech. 2004, 19 (4): 415-428.View ArticleGoogle Scholar
- Huberty CJ, Morris JD: Multivariate analysis versus multiple univariate analyses. Psychol Bull. 1989, 105 (2): 302-View ArticleGoogle Scholar
- Rosipal R, Krämer N: Overview and recent advances in partial least squares. Subspace, Latent Structure and Feature Selection. 2006, Berlin: Springer, 34-51.View ArticleGoogle Scholar
- Abdi H, Williams LJ: Partial least squares methods: partial least squares correlation and partial least square regression. Computational Toxicology. 2013, Berlin: Springer, 549-579.View ArticleGoogle Scholar
- Sadeghi H, Allard P, Duhaime M: Muscle power compensatory mechanisms in below-knee amputee gait. Am J Phys Med Rehabil. 2001, 80 (1): 25-32.View ArticlePubMedGoogle Scholar
- Powers CM, Rao S, Perry J: Knee kinetics in trans-tibial amputee gait. Gait Posture. 1998, 8 (1): 1-7.View ArticlePubMedGoogle Scholar
- Waters R, Perry J, Antonelli D, Hislop H: Energy cost of walking of amputees: the influence of level of amputation. J Bone Joint Surg. 1976, 58 (1): 42-46.PubMedGoogle Scholar
- Benjamini Y, Hochberg Y: Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Roy Stat Soc B. 1995, 57 (1): 289-300.Google Scholar
- Troje NF: Decomposing biological motion: a framework for analysis and synthesis of human gait patterns. J Vis. 2002, 2 (5): 371-387.View ArticlePubMedGoogle Scholar
- Alaqtash M, Sarkodie-Gyan T, Yu H, Fuentes O, Brower R, Abdelgawad A: Automatic classification of pathological gait patterns using ground reaction forces and machine learning algorithms. Engineering in Medicine and Biology Society, EMBC, 2011 Annual International Conference of the IEEE. 2011, Boston: IEEE, 453-457.View ArticleGoogle Scholar
- Barton J, Lees A: An application of neural networks for distinguishing gait patterns on the basis of hip-knee joint angle diagrams. Gait Posture. 1997, 5 (1): 28-33.View ArticleGoogle Scholar
- Begg R, Kamruzzaman J: A machine learning approach for automated recognition of movement patterns using basic, kinetic and kinematic gait data. J Biomech. 2005, 38 (3): 401-408.View ArticlePubMedGoogle Scholar
- Begg RK, Palaniswami M, Owen B: Support vector machines for automated gait classification. IEEE Trans Biomed Eng. 2005, 52 (5): 828-838.View ArticlePubMedGoogle Scholar
- Chau T: A review of analytical techniques for gait data. part 2: neural network and wavelet methods. Gait Posture. 2001, 13 (2): 102-120.View ArticlePubMedGoogle Scholar
- Holzreiter SH, Köhle ME: Assessment of gait patterns using neural networks. J Biomech. 1993, 26 (6): 645-651.View ArticlePubMedGoogle Scholar
- Kamruzzaman J, Begg RK: Support vector machines and other pattern recognition approaches to the diagnosis of cerebral palsy gait. IEEE Trans Biomed Eng. 2006, 53 (12): 2479-2490.View ArticlePubMedGoogle Scholar
- Köhle ME, Merkl D, Kastner J: Clinical gait analysis by neural networks: issues and experiences. Proceedings of the 10th IEEE Symposium on Computer-Based Medical Systems. 1997, Maribor: IEEE, 138-143.Google Scholar
- Lafuente R, Belda J, Sanchez-Lacuesta J, Soler C, Prat J: Design and test of neural networks and statistical classifiers in computer-aided movement analysis: a case study on gait analysis. Clin Biomech. 1998, 13 (3): 216-229.View ArticleGoogle Scholar
- Mannini A, Sabatini AM: Machine learning methods for classifying human physical activity from on-body accelerometers. Sensors. 2010, 10 (2): 1154-1175.View ArticlePubMedPubMed CentralGoogle Scholar
- Mezghani N, Husse S, Boivin K, Turcot K, Aissaoui R, Hagemeister N, de Guise JA: Automatic classification of asymptomatic and osteoarthritis knee gait patterns using kinematic data features and the nearest neighbor classifier. IEEE Trans Biomed Eng. 2008, 55 (3): 1230-1232.View ArticlePubMedGoogle Scholar
- Pogorelc B, Bosnić Z, Gams M: Automatic recognition of gait-related health problems in the elderly using machine learning. Multimed Tool Appl. 2012, 58 (2): 333-354.View ArticleGoogle Scholar
- Preece SJ, Goulermas JY, Kenney LP, Howard D, Meijer K, Crompton R: Activity identification using body-mounted sensors—a review of classification techniques. Physiol Meas. 2009, 30 (4): 1-View ArticleGoogle Scholar
- Simon SR: Quantification of human motion: gait analysis - benefits and limitations to its application to clinical problems. J Biomech. 2004, 37 (12): 1869-1880.View ArticlePubMedGoogle Scholar
- von Tscharner V, Enders H, Maurer C: Subspace identification and classification of healthy human gait. PLoS one. 2013, 8 (7): 65063-View ArticleGoogle Scholar
- Kaptein R, Daffertshofer A: UPMOVE: a Matlab Toolbox for the Analysis and Classification of Human Gait. [http://www.upmove.org]
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.