Economy, Movement Dynamics, and Muscle Activity of Human Walking at Different Speeds
Economy, Movement Dynamics, and Muscle Activity of Human Walking at Different Speeds
Economy, Movement Dynamics, and Muscle Activity of Human Walking at Different Speeds
com/scientificreports
The inherent intra-subject variability in human movements (i.e. cyclic movements like walking and running and
repeated discrete movements like reaching or throwing) has attracted growing interest within motor control and
motor learning research during the past four decades. Movement variability has been linked to sport perfor-
mance level, skill acquisition, motor control related pathology and ontogenies1–5. The variability may originate
from several sources such as the muscles, joints, soft tissue and central nervous system6,7. Thus, when the muscles
are activated in order to produce specific movements multiple processes are initiated, which all can be potential
sources to the variation in the final movement execution.
Dynamical system theory is a mathematical approach to explain the behaviour of complex systems including
biological systems like the human motor control system8,9. Dynamical system theory suggests that the multiple
variables within the human system (termed degrees of freedom) that are involved in the formation of movements
interact through a process termed self-organization in the creation of a coordinated and stabile movement pattern
(termed attractor state)1,10,11. An attractor can be characterized by both the spatial and temporal properties of the
exhibited variability4,12. In relation to human walking, a U-shaped relationship between walking speed and the
statistical persistency properties of the stride-to-stride time intervals has been observed13–15. A local minimum
in the statistical persistence of time stride intervals has been shown to coincide with the self-selected preferred
walking speed16,17. In line with this, it is well established that the metabolic cost of walking is minimized at the
preferred walking speed and increased at speeds above and below reflecting a U-shaped relationship between
walking speed and walking economy18,19.
Previous studies have separately investigated the relationship between walking speed and the rate of trajectory
divergence of joint angles and centre of mass movements using the largest Lyapunov exponent20,21. England and
Granata20 showed an increase in the rate of divergence of trajectories measured by the largest Lyapunov expo-
nent of the ankle, knee and hip joint angles with increasing speed. While Dingwell and Marin22 and Kang and
Dingwell23 showed increasing divergence of the trajectories of the centre of mass displacement with increasing
walking speed Bruijn et al.21 showed that this relationship was influenced by the movement direction. Stenum
et al.24 later showed that this discrepancy could be a result of methodological differences.
1
Department of Neuroscience and Pharmacology, University of Copenhagen, Denmark. 2Department of Electrical
Engineering, Technical University of Denmark, Denmark. Correspondence and requests for materials should be
addressed to P.C.R. (email: [email protected])
In agreement with the motor control theory proposed by Bernstein25, these previous observations indicate
that the dynamics of movements are not only dependent on the task related constraints (e.g. walking speed) but
also on the biomechanical constraints of the investigated structure (e.g. joints and centre of mass). However,
based on the aforementioned studies it is still an open question if the relationship between the joint angle and
centre of mass movement dynamics in terms of trajectory divergence and dimensionality and the walking speed
resembles the observed U-shaped relationship between walking economy and speed. Furthermore, muscle activ-
ity during locomotion has been extensively investigated in order to explain the underlying motor control (e.g.
reflex modulation and motor programs)26–31. However, it remains unknown if the movement dynamics and mus-
cle activity strategy at different walking speeds exhibit the same pattern.
Several different nonlinear analyses can be used to investigate the spatiotemporal structure of human variabil-
ity with each method assessing different characteristics of the time series in question32. The present study applies
both the largest Lyapunov exponent (LLE) and correlation dimension (CoD). The LLE quantifies the exponential
convergence or divergence of trajectories with time in state space and has been considered to be a measure of the
local dynamic stability4,33. The CoD quantifies the fractal dimensionality of the time series and has been used to
quantify how a system is organized in state space2,34. Thus, the methodological coupling of the LLE and CoD ena-
bles a detailed description of the dynamics of a system2,5. By applying this methodological approach in the present
study we seek a more refined understanding of the movement dynamics of human walking at different speeds.
Thus, the purpose of the present study was to investigate the relationship between movement dynamics and
walking speed. We assessed movement dynamics of the knee and ankle joint angles and the centre of mass accel-
erations at different walking speeds ranging across the speed considered as the most energy efficient. As men-
tioned previously, the U-shape relationship between walking speed and walking economy is well established in
the literature. The present study measured walking economy to verify this relationship. In addition, the muscle
activity pattern was assessed to evaluate how the movement dynamics is associated with the underlying motor
control.
Protocol. The study consisted of two experimental days. On the first day, standing anthropometrics, pre-
ferred walking speed (PWS), electromyography (EMG) and joint kinematics were measured during walking
at five different speeds. On the second day, oxygen uptake (VO2) was measured at identical walking speeds as
applied on the first day. Upon arrival to the laboratory on the first day the length of both legs of each participant
was measured as the distance from the trochanter major to the lateral malleolus and averaged across both legs.
Nondimensionalization of walking speeds through calculation of the Froude speed (FS) for each subject was
completed in order to normalize the walking speed in relation to leg length. This theoretical prediction of the
preferred walking speed (TPWS) was calculated as 42% of FS (equation 1)20.
FS = L⋅g (1)
L = length leg, g = 9.82 m/s .
2
EMG electrodes, foot switch and electro-goniometer were placed on the participants (see below) before a
5 minutes warm up walking session at a self-selected pace was completed. This was followed by a standardized
procedure of isometric maximal voluntary contractions (MVC) for the knee extensor and flexor muscles and
the ankle plantar and dorsiflexor muscles. During the knee extension and flexion the participants were sitting
upright with 100° hip flexion and 110° knee flexion (180° = full hip/knee extension). The waist, thigh, and ankle
were securely fastened to the seat. During the plantar flexion, the participants were standing upright on one leg
facing a wall bar. The participants took a firmly grip of the lowest reachable bar while they remained upright and
their knees fully extended which prevented heel raise and enabled an isometric contraction of the planter flexor
muscles. During maximal dorsiflexion, participants were seated with their back against a wall, with 90° of knee
flexion, 10° of ankle plantar flexion (0° = neutral standing position) and with the heels placed on the floor. The
foot position was manually fixed by the researcher during the contraction. For all four MVCs, maximal effort was
kept for three seconds under verbal encouragement. After a brief rest period, the procedure of determining the
PWS was conducted following the description by Dingwell and Marin22. The PWS was determined by gradually
decreasing and increasing the speed three times below and above the speed each participant reported as being
the most comfortable. The speed display was blinded to the participants and the speed reported as being the most
comfortable was noted. The average of the six noted speeds was calculated and reported as the PWS for each par-
ticipant. The PWS was determined to check if this differed significantly from the TPWS.
The participants wore a pair of light weight gymnastic shoes and walked for 12 minutes on a treadmill (HS-
1200 TechnoGym, Italy) at 20, 40, 100, 160 and 180% of their individual TPWS in randomized order, which
provided 180 to 700 strides. Between each walking speed, the participants had between 1–4 minutes of rest to
avoid fatigue.
On the second day, seven participants reported to the laboratory and completed the same warm up proto-
col and wore the same shoes as on the first day. The participants was fitted with the oxygen uptake face mask,
connected to the oxygen uptake recording device (see below) and walked for 6 minutes at 20, 40, 100, 160 and
180% of their individual TPWS in randomized order separated by 1–4 minutes of rest.
Measurements. Sagittal ankle and knee joint angles were measured using an electro-goniometer (Penny
& Giles, M-series) placed on the lateral side of each joint. The 3D centre of mass acceleration was estimated by
a tri-axial accelerometer (Marq-Medical, Farum, Denmark) placed on the sacrum fastened with sports tape.
The goniometer and accelerometer were connected to a small unit containing an amplifier and A/D converter
(20 × 10 × 5 mm) which was attached to the skin. The goniometer and accelerometer sensors had built-in low
pass filters of 100 Hz and 290 Hz, respectively, and both sensors were an integrated part of the system used for the
EMG recordings (see below).
Bipolar surface EMG electrode (2DT2 Foam Dual Pregelled Electrode, Multi Biosensors Inc., USA) were
mounted on the m. soleus (SOL), m. tibialis anterior (TA), m. vastus medialis (VM), and the m. biceps fem-
oris (BF) according to the recommendation of Perotto35. Micro-switches were placed under the heel and toe
to record the heel strike and toe-off events of walking. Wireless EMG sensors (MQair, Marq-Medical, Farum,
Denmark) were attached to the bipolar electrodes placed on SOL, TA, VM, BF muscles. Each EMG sensor con-
sisted of an amplifier (frequency response: 10–1000 Hz) and A/D converter (16 bit). In addition, signals from the
micro-switches placed under the heel and toe were also sampled by this system. Thus, the EMG, foot switch, accel-
erometer and goniometer signals were sampled synchronously at frequencies of 1000 Hz (EMG, foot switches)
and 333 Hz (goniometer/accelerometer), respectively. The signals were wirelessly transmitted and recorded by
an antenna connected to the USB port on a laptop. The signals were recorded by the software system Fireworks
1.1.0.35 (Marq-Medical, 2012, Farum, Denmark). The recordings were triggered by the foot switch placed under
the heel.
The oxygen uptake was continuously measured using an Oxycon Pro breath by breath gas analysing system
(Oxycon Pro, Jaeger, Wuerzburg, Germany) averaging the oxygen uptake every 5 second. Prior to the experiment,
the oxygen uptake system was calibrated to the oxygen and carbon dioxide content of a known gas. The oxygen
uptake data recorded during each of the 6 minutes walking trial was extracted for offline analysis.
Data analysis. The initial 90 seconds and final 30 seconds of each joint angle signals and the 3D acceleration
signals were discarded and the remaining time series were down sampled to 50 Hz. To quantify the variability of
each variable the data from 150 individual strides was time normalized (0–100%). Standard deviation was calcu-
lated across all strides at each time point and averaged over the normalized stride in accordance with Dingwell
and Marin22 as a measure of the mean variability (MeanSD).
To investigate the movement dynamics each of the down sampled time series included exactly 150 strides but
with a different number of data points as done by Myers and colleagues36. This methodological approach main-
tains the same number of data points/second for all subjects and walking speeds. An alternative approach is to
resample each stride to 100 data points as done by England and Granata20. To investigate the consequence of this
methodological choice, the LLE for the knee and ankle joint was calculated using both a fixed sampling frequency
and a resampling approach. Based on the results from this additional analysis presented in the Supplementary
material, we concluded that the methodological choice had a limited effect on the results presented in this study.
For each participant, the dynamics of the time series was investigated by calculating the LLE and CoD for the
two joint angles and the three acceleration time series obtained at each speed. The LLE measures the divergence
or convergence of trajectories of a time series in its state space33. A time series characterized by a random spati-
otemporal structure within the state space with rapid diverging data points will have a relatively high LLE. The
CoD is a measure of the organization of data points in state space and approximates the fractal dimension of the
region in the state space occupied by the dynamical system in question5,34. A time series characterized by a high
fractal dimensionality will have a relatively high CoD. In the present study, the algorithms from Wolf et al.33 and
Grassberger and Procaccia34 were used to calculate the LLE and the CoD, respectively. The calculation procedure
of these algorithms has been described in detail elsewhere33,34,37.
In order to calculate the LLE and CoD, the time series were reconstructed in the state space using the method
of delay embedding38–40. Figure 1 illustrates the organization of a time series in the state space, showing the trajec-
tories from 20 strides of the knee joint angle at the five speeds, for one representative participant folded in three
dimensions with the corresponding time lag. As previously done by Dingwell and Cusumano4 and Buzzi et al.2
the time delay (Tau) and embedding dimension (Dim) for delay embedding were calculated for each participant
and each speed using the Average Mutual Information and False Nearest Neighbour algorithm, respectively. The
group average of time delay and embedding dimension for each speed were calculated and used for the calcu-
lation of the LLE and CoD. The average, standard deviation, and range of both the time delay and embedding
dimension are presented in the Supplementary material. There was a general tendency to a higher embedding
dimension and time delay at speeds below 100% TPWS and constant values at 100% TPWS and above. Due to a
small inter-participant variation in embedding dimension and time delay but a relatively large inter-speed vari-
ation, group averaged values were used for each speed. To support this methodological choice, LLE for the knee
and ankle joint was calculated with both a group averaging of Tau and Dim and with the individual Tau and Dim.
The results are presented in the Supplementary material.
Surrogate analysis is a commonly used technique applied to evaluate the nature of the fluctuation in a time
series. It includes a test of the null hypothesis that fluctuations in a time series could originate from a linearly
auto-correlated Gaussian process41. The present study applied surrogate analysis to the measured variables across
the applied walking speeds2,4,42. For each original time series, 19 surrogate time series were constructed using the
pseudo periodic method presented by Small43. This surrogate method was shown to be more valid with joint angle
time series, which has an inherent periodic pattern compared to the Theiler’s surrogate algorithm41,42,44. The LLE
Figure 1. A representation of trajectories from 20 strides from one subject of the knee joint angle for each
speed (top = slowest, bottom = fastest) folded in three dimensions with corresponding time lag.
and CoD were calculated for each of the 19 surrogate data series. The mean value of the LLE and CoD from the
surrogate data was compared with that of the original time series.
The muscle activity strategy was quantified by calculating the mean muscle activity and levels of
co-contraction. The recorded EMG signals were transferred to Matlab for further treatment. The signals were
digitally high- and low-pass filtered (Butterworth fourth-order zero-lag digital filter, cut-off frequencies 20 Hz
and 500 Hz, respectively), full-wave rectified, and low pass filtered at 15 Hz to produce linear envelopes. The linear
envelopes were normalized to the maximal EMG amplitude of each muscle recorded during the MVCs.
The signal from the micro-switch on the heel was used to identify the heel strike (HS). The linear envelopes
were used to calculate a co-contraction index (CCI)45 around the HS with a window of 100 ms before HS and
200 ms after for each of the ankle and knee joint muscle pairs (TA/SOL and VM/BF). The CCI was calculated
according to the procedure described by Lewek et al.46 (equation 2):
200 ms postHS lower EMGi
CCI = ∫100 ms preHS higher EMGi
(lower EMG i + higher EMG i )
(2)
CCIs were calculated for 150 strides for each participant and a mean CCI for each of the muscle pairs was calcu-
lated and used as the input parameter for the statistical analysis.
The oxygen uptake data during the last three minutes of each walking trial was averaged and the walking econ-
omy was calculated by normalizing the oxygen uptake to the body mass and then subsequently normalizing this
to the walking speed (ml O2/min/kg/m/min = ml/kg/m) to render the cost of movement comparable at different
speeds as done by Foster and Lucia47.
Statistical analysis. Paired Student’s t-test was used to determine if the estimated 100% TPWS was signifi-
cantly different from the self-selected PWS. A one-way ANOVA for repeated measures was applied to investigate
the effect of speed (independent factor) on the dependent variables of MeanSD, LLE and CoD for knee and ankle
angles and centre of mass accelerations, EMG, co-contraction index and walking economy. In case of a signif-
icant effect of speed, a quadratic regression analysis was performed to determine the nature of the relationship
between the walking speed and dependent measure. P-values and the overall percentage of variance accounted
for by the regression (r2) were determined for each dependent variable. Furthermore, a Holm-Sidak post hoc
test was applied to evaluate the between-speed differences. The level of significance was set to 5%. In total, 1140
surrogate time series for each variable (5 speeds × 12 participants × 19 surrogate time series) were created. For
each participant, all variables at each speed were compared to the 95% confidence interval of the corresponding
surrogate variable. All statistical analyses were performed using the Sigmaplot (Systat Software, Inc. 2014) and
Matlab (MathWorks R2011b).
Results
Theoretical preferred walking speed (TPWS) and preferred walking speed (PWS). An average
PWS of 4.69 km/h (SD = 0.47 km/h) was observed and this was not significantly different from the 100% TPWS
of 4.43 km/h (SD = 0.09 km/h) (p = 0.108).
MeanSD of joint angles and body mass acceleration. There was a significant effect of speed on the
MeanSD for both joint angles (p < 0.001 in both cases). The quadratic curvilinear fit was also statistically sig-
nificant (p < 0.001 in both cases) and walking speed could explain 48% of the variance (Fig. 2). The MeanSD of
both joint angles were significantly higher at 20% TPWS compared to higher walking speeds (p < 0.001 for all
comparisons). The ankle MeanSD at 40% TPWS was significantly higher compared to 100% and 160% TPWS
(p = 0.01 and p = 0.019, respectively) but did not differ from 180% TPWS. The knee MeanSD at 40% TPWS was
significantly higher compared to 100% TPWS (p = 0.022) but did not differ from higher walking speeds. No other
between-speed differences were observed for the ankle and knee MeanSD.
There was a significant effect of speed on the MeanSD for the centre of mass acceleration in all directions
(p < 0.001 in all cases). The quadratic curvilinear fit was significant (p < 0.001 for all three fits) and showed an
increasing pattern in MeanSD with increase in walking speed. Walking speed could explain 86% to 91% of the
variance (Fig. 2). The post hoc test showed no significant difference in MeanSD for the anterior-posterior and
mediolateral direction between 20% and 40% TPWS and between 40% and 100% TPWS for the anterior-posterior
direction. All other between-speed comparisons showed a significant difference (p ≤ 0.014 for all comparisons).
Nonlinear analysis of joint angles. There was a significant effect of walking speed on the LLE and CoD
of the ankle joint angle (p < 0.001 for both angles). The quadratic curvilinear fit was significant for both the LLE
and CoD (p < 0.001) and the walking speed explained 29% and 83% of the variance, respectively (Fig. 3). The LLE
at 40% TPWS was significantly lower compared to the higher walking speeds (p ≤ 0.018 for all comparisons). At
100% TPWS the LLE was significantly lower than at 160% and 180% TPWS (p = 0.009 and p = 0.02, respectively).
No other between-speed differences were observed for the LLE of the ankle joint angle. There were significant dif-
ferences for all between-speed comparisons for the CoD of the ankle joint angles (p ≤ 0.003 for all comparisons)
except between 160% and 180% TPWS.
There was a significant effect of walking speed on the LLE and CoD of the knee joint angle (p = 0.009 for LLE
and p < 0.001 for CoD). The quadratic curvilinear fit was significant (p = 0.005 for LLE and p < 0.001 for CoD)
and walking speed explained 16% and 67% of the variance in the LLE and CoD, respectively (Fig. 3). The LLE
of the knee joint angle was significantly lower at 100% TPWS compared to 20% TPWS (p = 0.007). No other
between-speed differences were observed. The CoD at 20% and 40% TPWS was significantly higher compared
to the higher walking speeds (p < 0.001 for all comparisons). No other statistically significant differences were
observed.
Nonlinear analysis of centre of mass acceleration. There was a significant speed effect for both the
LLE and CoD of the centre of mass accelerations in all three directions (p < 0.001). The quadratic curvilinear fits
were also significant (p < 0.001 in all cases) and walking speed explained between 25% and 58% of the variance for
the LLE and between 85% and 93% of the variance for the CoD (Fig. 4). The LLE of the anterior-posterior centre
Figure 2. MeanSD for the ankle and knee joint angles and the AP, ML and VT centre of mass accelereation.
Error bars indicate between-subject standard deviation. Curve fit lines represent quadratic polynomial
regression curves with r2 values indicate the percent of variance accounted for by each regression model.
*Indicates significant quadratic relationship between walking speed and variable.
Figure 3. Largest Lyapunov exponent and correlation dimension of the ankle and knee joint angle. Error
bars indicate between-subject standard deviation. Curve fit lines represent quadratic polynomial regression
curves with r2 values indicate the percent of variance accounted for by each regression model. *Indicates
significant quadratic relationship between walking speed and variable.
of mass acceleration was significantly higher at 20% TPWS compared to 100 and 160% TPWS (p = 0.005, 0.042,
respectively) and higher at 40% TPWS compared to 100% TPWS (p = 0.025). The CoD of the anterior-posterior
centre of mass acceleration was significantly higher at the two lowest walking speeds compared to the faster
walking speeds (p < 0.001 in all cases). In addition, the CoD at 100% TPWS was significantly higher compared to
180% TPWS (p = 0.0016). No other statistically significant between-speed differences were observed.
The LLE of the mediolateral centre of mass acceleration was significantly higher at the lowest walking speed
compared to the higher walking speeds (Fig. 4, p < 0.001 in all cases). Furthermore, the LLE was significantly
lower at 100% TPWS compared to the two higher walking speeds (p = 0.007 in both cases). The CoD of the medi-
olateral centre of mass acceleration decreased significantly with each increment in walking speed (p ≤ 0.013 in all
cases) except from 160% to 180% TPWS (Fig. 4).
The LLE of the vertical centre of mass acceleration was significantly higher at the lowest walking speed com-
pared to the higher walking speeds (p < 0.001 in all cases). Furthermore, the LLE at 40% TPWS was significantly
lower than at 180% TPWS (p = 0.003). The CoD of the vertical centre of mass acceleration decreased significantly
with each increment in walking speed (p ≤ 0.013 in all cases) except from 160% to 180% TPWS.
Surrogate analysis. The surrogate analysis of the joint angles showed that 100% of the LLE calculated on
the original ankle joint angle time series were lower than the 95% confidence interval of the LLE calculated on the
corresponding surrogates. For the knee joint angle, 91.7% of the LLE calculated on the original knee joint angle
time series were lower than the 95% confidence interval of the LLE calculated on the corresponding surrogates.
When comparing the CoD calculated on the original and corresponding surrogates, the CoD from 43.3% of the
ankle joint angle time series and from 46.7% of the knee joint angle time series were lower than the 95% confi-
dence interval of the CoD from the surrogates.
The surrogate analysis of the centre of mass accelerations signals showed that between 98.3% and 100% of
the LLE calculated on the original time series were lower than the 95% confidence interval the LLE from the
corresponding surrogates. Equally, between 95% and 100% of the CoD calculated on the original centre of mass
acceleration time series were lower than the 95% confidence interval of the CoD calculated on the corresponding
surrogates.
Figure 4. Largest Lyapunov exponent and correlation dimension for anterior-posterior, medio-lateral
and vertical direction of centre of mass accerelation. Error bars indicate between-subject standard deviation.
Curve fit lines represent quadratic polynomial regression curves with r2 values indicate the percent of variance
accounted for by each regression model. *Indicates significant quadratic relationship between walking speed
and variable.
Muscle activity. There was a significant effect of speed on the muscle activity level of all four muscles
(p < 0.001). The quadratic fit was also significant for all four muscles (p < 0.001) and walking speed explained
between 40% and 61% of the variance (Fig. 5). The VM activity was significantly higher at 160 and 180% TPWS
compared to the three lower walking speeds (p ≤ 0.005 for all comparisons) but did not differ significantly
between the three lowest or between the two highest walking speeds. The muscle activity of both BF and TA were
significantly higher at the two highest walking speeds compared to the three lower walking speeds (p < 0.001
for all comparisons). In addition the activity was significantly higher at 180% TPWS compared to 160% TPWS.
The muscle activity of the SOL increased significantly from 40% to 100% TPWS and from 100% to 160% TPWS
(p ≤ 0.012 in both cases). No significant differences were observed between 20% and 40% TPWS and between
160% and 180% TPWS.
Figure 5. Muscle activity and co-contraction index for each muscles and muscle pairs. Error bars indicate
between-subject standard deviation. Curve fit lines represent quadratic polynomial regression curves with r2
values indicate the percent of variance accounted for by each regression model. *Indicates significant quadratic
relationship between walking speed and variable.
There was a significant effect of speed on the co-contraction index of the VM and BF (p < 0.001) with a
significant quadratic fit (p < 0.001) and 38% of the variance was explained by the walking speed (Fig. 5). The
co-contraction index was significantly higher at the two highest walking speeds compared to the three lowest
walking speeds (p ≤ 0.011). Furthermore, the co-contraction index was significantly higher at 180% TPWS com-
pared to 160% TPWS (p = 0.02). There was an overall effect of walking speed on the co-contraction index of the
TA and SOL (p = 0.024). However, the quadratic fit was not statistically significant and only 7% of the variance
was explained by the walking speed (Fig. 5). The post hoc test revealed no statistically significant between-speed
differences.
Walking economy. There was an overall effect of walking speed on walking economy (p < 0.001). The quad-
ratic fit was significant (p < 0.001) and 85% of the variance was explained by the walking speed (Fig. 6). The
walking economy was significantly higher at the two lowest walking speeds compared to the three higher speeds
Figure 6. Walking economy for each walking speed. Error bars indicate between-subject standard deviation.
Curve fit lines represent quadratic polynomial regression curves with r2 values indicate the percent of variance
accounted for by each regression model. *Indicates significant quadratic relationship between walking speed
and walking economy.
(p < 0.001 for all comparisons). Furthermore, the walking economy at 100% TPWS was significantly lower com-
pared to 180% TPWS. No other between-speed differences were observed.
Discussion
The present study aimed to investigate the relationship between the movement dynamics (assessed for the knee
and ankle joint angles and the centre of mass accelerations) and walking speed. We observed an intermediate state
in the dynamics of the anterior-posterior and medio-lateral centre of mass acceleration and the knee joint angle
at 100% TPWS corresponding to speed where there was a minimum in walking economy. At this walking speed
the LLE was relative low compared to walking speeds above and below and the CoD was in-between the values
observed at speeds above and below. Regarding the ankle joint movement dynamics and muscle activation strat-
egy, the results were more differential which may be due to differences in the anatomy and functional demands
of the knee and ankle joints.
In the present study, the dynamics of knee and ankle joint angles and centre of mass accelerations was quanti-
fied by the LLE and CoD. These two measures quantify different characteristics of the time series. CoD quantifies
the fractal dimensionality of the time series unfolded in the state space and provides a measure of the spatial
organization based on the temporal evolution of the time series. A low value could reflect that the time series
is organized in a tighter fashion compared to a high value. The LLE on the other hand quantifies the rate at
which the trajectories diverge or converge in state space. Thus, it is a measure of changes in the time series when
unfolded in the state space. A low value means small changes over time, and a high value means larger changes
over time. The combination of CoD and the LLE provides valuable information of the structure of the time
series. High CoD and LLE indicate a less organized structure with rapid changes. In contrast, low values in both
parameters indicate a more organized structure with less rapid changes. These two extremes could characterize a
system as either randomly or periodically structured. An intermediate (i.e. chaotic) structure has been suggested
to be linked with movement attractors observed in young and healthy humans in contrast to the elderly and/or
diseased12,36.
Several studies have investigated different biomechanical parameters during walking at different speeds and
different methods have been used to determine the investigated speeds. Bruijn et al.21 used five absolute speeds
ranging from 0.62 m/s to 1.72 m/s with an inter-speed interval of 0.22 m/s. Jordan et al.14 used five percentages
of PWS ranging from 80% to 120%. In the present study, the investigated speed was determined as 42% of the
FS as done by England and Granata20. This method provided a feasible and valid estimate of the theoretical pre-
dicted preferred walking speed which also appeared to be comparable to the self-perceived PWS reported by the
participants.
The variability in joint angles and centre of mass acceleration was measured by MeanSD across all 150 strides.
Thus, MeanSD quantifies the average amount of variation in joint movements and centre of mass acceleration
within each stride but does not take into account the order of strides. MeanSD can be considered to be a measure
of the consistency where low values indicate high consistency and high values indicate low consistency. The joint
angles and centre of mass accelerations showed opposite patterns. The consistency of the joint angles was low
at the lowest speeds and high at the highest velocities which confirms previous observations48. In contrast, the
consistency of the centre of mass accelerations in all directions decreased with walking speed. The walking speed
dependency of the joint angle variability observed in the present study resembles that observed by Jordan and
colleagues on the normalized variability (measured as coefficient of variance) in stride length and step length14.
Based on this, it could be speculated that the consistency in lower limb joint movements in the sagittal plane is
closely related to the consistency of step and stride length. In the same study, the authors observed an increase
in ground reaction force consistency with walking speed which is well in line with the increasing centre of mass
acceleration variability across speeds observed in the present study14. With respect to the movement of the centre
of mass, the results of the present study are in contrast to other observations49. Dingwell and Marin reported a
significant quadratic curvilinear fit between walking speed and the MeanSD of the velocity of the upper body
(the first thoracic vertebrae) where between 11% and 28% of variance could be explained by the regression model
and with a local minimum in MeanSD at PWS49. The present study could not confirm the U-shaped relationship
suggested by the authors of the aforementioned study. This discrepancy could be explained by methodological
differences.
The dynamics of the joint angles was strongly dependent on both the joint in question and the changes in
speed. The CoD of both joints decreased with increase in walking speed, indicating a more tightly organized
structure at higher speeds. The LLE of the knee joint angle showed tendency to a U-shape relationship indicating
rapid changes in the trajectories at both lower and higher speeds. This is visualized in Fig. 1, where the knee joint
angle at the slowest speeds reflected a relatively random pattern with limited structure. At 100% TPWS the knee
joint angle trajectory exhibited a more distinct pattern with a tight organization. This pattern became less smooth
and with more rapid changes with increasing speed.
A different pattern was observed for the ankle. The LLE at 20% TPWS was significantly higher when com-
pared to 40% TPWS but the CoD at these speeds did not differ. This indicates that both walking conditions had
relatively unorganized structures in the state space but the slowest speed induced much more rapid changes in
the trajectories. This is potentially due to the functional characteristics of the ankle joint, and the differences in
the movement task solved by the joint. During one-legged balance, a large portion of movement control of the
centre of mass is located at the ankle joint50,51 and the subtalar joint is partly responsible for the medio-lateral
movements. It is likely that during the slowest speed, the task of maintaining medio-lateral balance in the subtalar
joint interferes with the dorsi/plantar-flexion of the talocrural joint, resulting in rapid changes in the trajectories
quantified by the relatively high LLE value. As speed increases, the challenge to maintain medio-lateral balance
decreases, which may explain the reduced LLE in the sagittal plane. As the speed increases above 100% TPWS,
the impact increases, and due to its role as the first major shock absorber in the leg; rapid changes will be induced
to the ankle joint angle trajectories. Our joint angle results are partly in agreement with the results presented by
England and Granata20. Within the comparable speeds used by both England and Granata20 and the present study,
the LLE for the ankle joint angle showed the same tendency to an increase with increasing speed. However, the
increase in LLE for the knee joint angle observed by England and Granata20 could not be confirmed by the pres-
ent study. This discrepancy could possibly be explained by differences in the applied embedding dimensions, the
algorithm to estimate the LLE, number of strides and the normalization technique24.
When comparing the dynamics of the centre of mass accelerations, the LLE for the anterior-posterior direc-
tion best resembled the U-shaped curve observed in walking economy. When combined with decay in the CoD,
the anterior-posterior acceleration at 100% TPWS was characterized by a relative tight organization with slower
changes. At a lower speed, the acceleration seemed to become less tightly organized and with more rapid changes
and at a higher speed, the rate of divergence increased again. The medio-lateral and vertical accelerations of
the centre of mass showed a slightly different relationship with speed. Although the pattern with decreasing
CoD and thereby a more tightly organized structure was seen in all three directions, the LLE however, revealed
differences. At the slowest speed, both the medio-lateral and vertical acceleration showed very rapid changes in
the trajectories. It is possible that this is due to the difficulties of walking at a very slow speed, which in our case
almost resembled a one-legged, postural balance task. This task induced many small and rapid adjustments of
the position of the centre of mass not directly related to moving the centre of mass forward. At higher speeds the
medio-lateral acceleration was also characterized by more rapid changes. Thus, it seemed that slow walking was
linked to a decreased adaptability through a less organized structure with rapid changes while faster walking was
linked to a tighter organization with rapid changes. Together, these observations indicated that the local mini-
mum in walking economy coincided with a structure of the centre of mass anterior-posterior and medio-lateral
acceleration that could be characterized as an intermediate stage somewhere between a loosely organized system
with rapid changes and a very tightly organized system with rapid changes. In line with a previously presented
model of human movement variability by Stergiou and colleagues, we suggest that this intermediate stage reflects
an optimal condition, where the dynamics of the system provides a high adaptability and robustness towards
external perturbations12,36. It should be mentioned that the dynamics of the knee joint angle had a similar inter-
mediate stage at 100% TPWS, which could indicate that the movement of that joint angle also possess a high
adaptability at that walking speed.
Bruijn et al.21 calculated the LLE on the displacement trajectories of the centre of mass during walking in a
range of speeds. Three different patterns were observed for the three directions of the centre of mass. The LLE
of the displacement trajectories in the anterior-posterior direction decreased with increasing speed. A tendency
to an inverted U-relationship was observed in the medio-lateral direction and an increase was observed for the
vertical direction with increasing speed. Additionally, Dingwell and Marin22 and Kang and Dingwell23 showed
increasing divergence of the trajectories of the centre of mass displacement with increasing walking speed. We
were not able to reproduce the findings reported by Bruijn et al.21 Dingwell and Marin22 and Kang and Dingwell23.
This discrepancy could likely be due to methodological difference (e.g. choice of LLE algorithm and stride nor-
malization procedure)24.
The muscle activity reflects the functional role of each muscle. All four muscles showed the same increasing
pattern with increasing speed. However, TA and SOL increased more rapidly. With increasing speed, the need
for increased propulsion is accounted for by increased activity in the SOL52. This may also raise the need for both
rapid toe lift during the swing phase and the control of plantar flexion at heel strike, all done by TA53. The BF and
VM were hardly active at or below 100% TPWS while the activities of these muscles were increased at higher
speeds suggesting an increased need for shock absorption. This is also reflected in the co-contraction index which
followed the same pattern. The co-contraction index was calculated for the period just around heel strike, where
the impact of the ground contact is absorbed. For the distal joint the muscle pair furthermore needs to prepare
for the balance task by increasing the joint stability54. Thus, we suggest that the co-contraction index reflects two
tasks maintained by the ankle joint around heel strike: shock absorption and balance control at low speeds and
mainly shock absorption at higher speeds. At higher speeds the proximal muscle pairs contributed substantially
to the shock absorption55.
The present study measured oxygen uptake in order to verify that the U-shaped relationship between walking
speed and walking economy previously established in young healthy individuals also existed in the participants
included in the present study. This relationship could be confirmed.
Before calculating the LLE and CoD the time series are reconstructed in state space using the embedding
dimension and time lag. In the present study, a group averaged embedding dimension and time lag for each speed
were used as previously done4,20,21,56. An alternative approach is to use the individual determined embedding
dimension and time lag for each time series. In the present study, this approach would resolve in (12 partici-
pants × 5 speeds × 5 variables) 300 unique state spaces compared to the (1 × group × 5 speeds × 5 variables) 25
state spaces used. Van Schooten and colleagues57 investigated the test-retest reliability of calculation of LLE from
the centre of mass acceleration during walking using both the individual and group averaging approach when
calculating embedding dimension and time lag for state space reconstruction. Based on intra-class correlations
and smallest detectable differences the authors concluded that the group averaging approach was the most appro-
priate57. Based on the results presented in the Supplemental material where no significant differences in the LLE
results were observed between the two methods, we concluded that the applied method was valid.
The LLE has been widely used to quantify the dynamics of walking in a number of studies2,4,49,56,58,59 with
two dominating algorithms: the Wolf algorithm33 and the Rosenstein algorithm60. The Wolf algorithm has been
proven to be more sensitive to detect age-related and joint-related differences during walking compared to the
Rosenstein algorithm37. Based on the differences between the two algorithms described in detail by Cignetti
et al.37 and Bruijn et al.61 and the discussion of the sensitivity of the algorithm in Cignetti et al.37, Bruijn et al.61 and
Cignetti et al.62, we decided to use the Wolf algorithm.
Since the LLE has been shown to be sensitive to the number of strides investigated63, we decided to adjust the
time series to contain an equal number of 150 strides for all participants and speeds. To the best of our knowledge
no consensus exists regarding the normalization process of the time series used for the LLE. To avoid differences
in the number of data points used in the calculation, studies have normalized time series either to the same
total number of points20,37,64 or normalized each stride to a given number of points20,49. However, this procedure
rescales the time series and could potentially hide the time dependent behaviour of the system. The aim of the
present study was to investigate the effect of different walking speeds on the movement dynamics. One major
change in the movement solution is a decreasing stride time with increasing speed. Thus, the number of time
points available for the system to adjust the behaviour is greatly changed with increasing speed. Interpolating the
time series and adding or removing data points will potentially hide behavioural characteristics of the trajectory
in state space. Thus, we chose not to rescale the time series36,56,65. The analysis presented in the supplemental
material did reveal a significant difference in the LLE of the knee but not of the ankle joint angle when comparing
the results based on the applied method (fixed sampling frequency with different number of data points versus
an alternative method – using normalized time series with an equal number of data points). However, the overall
pattern of the LLE across the different speeds was qualitatively similar for the two methods. While this supports
the chosen methodology in the present study, it should be noted that the Supplementary material did not include
the centre of mass acceleration signals or the correlation dimension analyses. Thus, a potential effect of the nor-
malization technique on these results cannot be excluded.
In the present study, walking economy was measured from a subset of the subjects and on a different day
than the kinematics and muscle activity. Even though this could be considered a limitation of the present study,
the presented results confirmed what has been previously reported in the literature18,19. In addition, day-to-day
variations in walking economy have been shown to be modest66. Thus, we consider these factors to have a limited
influence on the results.
In conclusion, we found that at 100% TPWS the walking economy was minimized and the dynamics of the
anterior-posterior, medio-lateral centre of mass acceleration and the knee joint angle exhibited an intermediate
stage. We interpret this as a stage of optimal variability of the human system meaning that it has a high degree
of adaptability. This stage also appears to be the most energy-efficient. Furthermore, the dynamics of the joint
angle trajectories and the muscle activation strategy were closely linked to the functional role and biomechanical
constraints of the joints.
References
1. Handford, C., Davids, K., Bennett, S. & Button, C. Skill acquisition in sport: some applications of an evolving practice ecology.
Journal of sports sciences 15, 621–640 (1997).
2. Buzzi, U. H., Stergiou, N., Kurz, M. J., Hageman, P. A. & Heidel, J. Nonlinear dynamics indicates aging affects variability during gait.
Clinical biomechanics 18, 435–443 (2003).
3. Stergiou, N. & Decker, L. M. Human movement variability, nonlinear dynamics, and pathology: is there a connection? Hum Mov Sci
30, 869–888 (2011).
4. Dingwell, J. B. & Cusumano, J. P. Nonlinear time series analysis of normal and pathological human walking. Chaos 10, 848–863
(2000).
5. Harbourne, R. T. & Stergiou, N. Nonlinear analysis of the development of sitting postural control. Developmental psychobiology 42,
368–377 (2003).
6. Hausdorff, J. M. et al. Etiology and modification of gait instability in older adults: a randomized controlled trial of exercise. Journal
of applied physiology (Bethesda, Md:1985) 90, 2117–2129 (2001).
7. Hausdorff, J. M. Gait variability: methods, modeling and meaning. Journal of neuroengineering and rehabilitation 2, 19 (2005).
8. Glass, L. & Mackey, M. C. From Clocks to Chaos: The rhythms of Life. (Princeton University Press, 1988).
9. Davids, K., Bennett, S. & Newell, K. M. Movement System Variability. (Human Kinectics, 2006).
10. Kelso, J. A. S. & Schöner, G. Self-organization of coordinative movement patterns. Human Movement Science 7, 27–46 (1988).
11. Barrett, N. F. A dynamic systems view of habits. Frontiers in human neuroscience 8, 682 (2014).
12. Stergiou, N., Harbourne, R. & Cavanaugh, J. Optimal movement variability: a new theoretical perspective for neurologic physical
therapy. Journal of neurologic physical therapy: JNPT 30, 120–129 (2006).
13. Hausdorff, J. M., Peng, C. K., Ladin, Z., Wei, J. Y. & Goldberger, A. L. Is walking a random walk? Evidence for long-range correlations
in stride interval of human gait. J Appl Physiol 78, 349–358 (1995).
14. Jordan, K., Challis, J. H. & Newell, K. M. Walking speed influences on gait cycle variability. Gait & posture 26, 128–134 (2007).
15. Chien, J. H., Yentes, J., Stergiou, N. & Siu, K. C. The Effect of Walking Speed on Gait Variability in Healthy Young, Middle-aged and
Elderly Individuals. Journal of physical activity, nutrition and rehabilitation 2015 (2015).
16. Jordan, K., Challis, J. H., Cusumano, J. P. & Newell, K. M. Stability and the time-dependent structure of gait variability in walking
and running. Hum Mov Sci 28, 113–128 (2009).
17. Jordan, K. & Newell, K. M. The structure of variability in human walking and running is speed-dependent. Exerc Sport Sci Rev 36,
200–204 (2008).
18. Ralston, H. J. Energy-speed relation and optimal speed during level walking. Internationale Zeitschrift fur angewandte Physiologie,
einschliesslich Arbeitsphysiologie 17, 277–283 (1958).
19. Zarrugh, M. Y., Todd, F. N. & Ralston, H. J. Optimization of energy expenditure during level walking. European journal of applied
physiology and occupational physiology 33, 293–306 (1974).
20. England, S. A. & Granata, K. P. The influence of gait speed on local dynamic stability of walking. Gait & posture 25, 172–178 (2007).
21. Bruijn, S. M., van Dieen, J. H., Meijer, O. G. & Beek, P. J. Is slow walking more stable? Journal of biomechanics 42, 1506–1512, doi:
10.1016/j.jbiomech.2009.03.047 (2009).
22. Dingwell, J. B. & Marin, L. C. Kinematic variability and local dynamic stability of upper body motions when walking at different
speeds. Journal of biomechanics 39, 444–452, doi: 10.1016/j.jbiomech.2004.12.014 (2006).
23. Kang, H. G. & Dingwell, J. B. Effects of walking speed, strength and range of motion on gait stability in healthy older adults. Journal
of biomechanics 41, 2899–2905, doi: 10.1016/j.jbiomech.2008.08.002 (2008).
24. Stenum, J., Bruijn, S. M. & Jensen, B. R. The effect of walking speed on local dynamic stability is sensitive to calculation methods.
Journal of biomechanics 47, 3776–3779, doi: 10.1016/j.jbiomech.2014.09.020 (2014).
25. Bernstein, N. The co-ordination and regulation of movements. (Pergamon, 1967).
26. Shiavi, R., Bugle, H. J. & Limbird, T. Electromyographic gait assessment, Part 1: Adult EMG profiles and walking speed. Journal of
rehabilitation research and development 24, 13–23 (1987).
27. Ivanenko, Y. P., Poppele, R. E. & Lacquaniti, F. Five basic muscle activation patterns account for muscle activity during human
locomotion. The Journal of physiology 556, 267–282, doi: 10.1113/jphysiol.2003.057174 (2004).
28. Shiavi, R. Electromyographic patterns in adult locomotion: a comprehensive review. Journal of rehabilitation research and
development 22, 85–98 (1985).
29. Nielsen, J. B. How we walk: central control of muscle activity during human walking. The Neuroscientist : a review journal bringing
neurobiology, neurology and psychiatry 9, 195–204 (2003).
30. Petersen, T. H., Willerslev-Olsen, M., Conway, B. A. & Nielsen, J. B. The motor cortex drives the muscles during walking in human
subjects. The Journal of physiology 590, 2443–2452, doi: 10.1113/jphysiol.2012.227397 (2012).
31. Kang, H. G. & Dingwell, J. B. Dynamics and stability of muscle activations during walking in healthy young and older adults. Journal
of biomechanics 42, 2231–2237, doi: 10.1016/j.jbiomech.2009.06.038 (2009).
32. Stergiou, N. Innovative analyses of human movement - Analytical tools for human movement research. (Human Kinetics, 2004).
33. Wolf, A., Swift, J. B., Swinney, H. L. & Vastano, J. A. Determining Lyapunov Exponents from a Time-Series. Physica D 16, 285–317
(1985).
34. Grassberger, P. & Procaccia, I. Measuring the Strangeness of Strange Attractors. Physica D 9, 189–208 (1983).
35. Perotto, A. O. Anatomical guide for the electromyographer: the limbs and trunk. 4th edn (Charles C Thomas, 2009).
36. Myers, S. A., Pipinos, I. I., Johanning, J. M. & Stergiou, N. Gait variability of patients with intermittent claudication is similar before
and after the onset of claudication pain. Clinical biomechanics 26, 729–734 (2011).
37. Cignetti, F., Decker, L. M. & Stergiou, N. Sensitivity of the Wolf ’s and Rosenstein’s algorithms to evaluate local dynamic stability
from small gait data sets. Annals of biomedical engineering 40, 1122–1130 (2012).
38. Takens, F. Detecting strange attractors in turbulence. Dynamical Systems and Turbulence, Lecture Notes in Mathematics 898, 366–381
(1981).
39. Sauer, T., Yorke, J. A. & Casdagli, M. Embedology. J Stat Phys 65, 579–616 (1991).
40. Sauer, T. & Yorke, J. A. How many delay coordinates do you need? Int J Bifurc Chaos 3, 737–744 (1993).
41. Theiler, J., Eubank, S., Longtin, A., Galdrikian, B. & Farmer, J. D. Testing for nonlinearity in time series: the method of surrogate
data. Physica D 58, 77–94 (1992).
42. Miller, D. J., Stergiou, N. & Kurz, M. J. An improved surrogate method for detecting the presence of chaos in gait. Journal of
biomechanics 39, 2873–2876 (2006).
43. Small, M., Yu, D. & Harrison, R.G. Surrogate test for pseudoperiodic time series data. Physical Review Letters 87, 188101–188104
(2001).
44. Theiler, J. & Rapp, P. E. Re-examination of the evidence for low-dimensional, nonlinear structure in the human
electroencephalogram. Electroencephalography and clinical neurophysiology 98, 213–222 (1996).
45. Lewek, M. D., Scholz, J., Rudolph, K. S. & Snyder-Mackler, L. Stride-to-stride variability of knee motion in patients with knee
osteoarthritis. Gait & posture 23, 505–511 (2006).
46. Lewek, M. D., Rudolph, K. S. & Snyder-Mackler, L. Control of frontal plane knee laxity during gait in patients with medial
compartment knee osteoarthritis. Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society 12, 745–751 (2004).
47. Foster, C. & Lucia, A. Running economy: the forgotten factor in elite performance. Sports medicine (Auckland, NZ) 37, 316–319
(2007).
48. Oberg, T., Karsznia, A. & Oberg, K. Joint angle parameters in gait: reference data for normal subjects, 10–79 years of age. Journal of
rehabilitation research and development 31, 199–213 (1994).
49. Dingwell, J. B., Cusumano, J. P., Cavanagh, P. R. & Sternad, D. Local dynamic stability versus kinematic variability of continuous
overground and treadmill walking. Journal of biomechanical engineering 123, 27–32 (2001).
50. King, D. L. & Zatsiorsky, V. M. Periods of extreme ankle displacement during one-legged standing. Gait & posture 15, 172–179
(2002).
51. Hoogvliet, P., van Duyl, W. A., de Bakker, J. V., Mulder, P. G. & Stam, H. J. Variations in foot breadth: effect on aspects of postural
control during one-leg stance. Archives of physical medicine and rehabilitation 78, 284–289 (1997).
52. McGowan, C. P., Neptune, R. R. & Kram, R. Independent effects of weight and mass on plantar flexor activity during walking:
implications for their contributions to body support and forward propulsion. Journal of Applied Physiology 105, 486–494 (2008).
53. Winter, D. A. & Yack, H. J. EMG profiles during normal human walking: stride-to-stride and inter-subject variability.
Electroencephalography and clinical neurophysiology 67, 402–411 (1987).
54. Nielsen, J. & Kagamihara, Y. The regulation of presynaptic inhibition during co-contraction of antagonistic muscles in man. The
Journal of physiology 464, 575–593 (1993).
55. Hamill, J., Derrick, T. R. & Holt, K. G. Shock attenuation and stride freqency during runnig. Hum Mov Sci 14, 45–60 (1995).
56. Wurdeman, S. R., Myers, S. A. & Stergiou, N. Amputation effects on the underlying complexity within transtibial amputee ankle
motion. Chaos 24, doi: 10.1063/1.4869580 (2014).
57. van Schooten, K. S., Rispens, S. M., Pijnappels, M., Daffertshofer, A. & van Dieen, J. H. Assessing gait stability: the influence of state
space reconstruction on inter- and intra-day reliability of local dynamic stability during over-ground walking. Journal of
biomechanics 46, 137–141, doi: 10.1016/j.jbiomech.2012.10.032 (2013).
58. Buzzi, U. H. & Ulrich, B. D. Dynamic stability of gait cycles as a function of speed and system constraints. Motor Control 8, 241–254
(2004).
59. Dingwell, J. B., Cusumano, J. P., Sternad, D. & Cavanagh, P. R. Slower speeds in patients with diabetic neuropathy lead to improved
local dynamic stability of continuous overground walking. Journal of biomechanics 33, 1269–1277 (2000).
60. Rosenstein, M. T., Collins, J. J. & De Luca, C. J. A Practical Method for Calculating Largest Lyapunov Exponents from Small Data
Sets. Physica D-Nonlinear Phenomena 65, 117–134 (1993).
61. Bruijn, S. M., Meijer, O. G., Rispens, S. M., Daffertshofer, A. & van Dieen, J. H. Letter to the editor: “Sensitivity of the Wolf ’s and
Rosenstein’s algorithms to evaluate local dynamic stability from small gait data sets”. Annals of biomedical engineering 40, 2505–2506
(2012).
62. Cignetti, F., Decker, L. M. & Stergiou, N. Sensitivity of the Wolf ’s and Rosenstein’s Algorithms to Evaluate Local Dynamic Stability
from Small Gait Data Sets: Response to Commentaries by Bruijn et al. Annals of biomedical engineering 40, 2507–2509 (2012).
63. Bruijn, S. M., van Dieen, J. H., Meijer, O. G. & Beek, P. J. Statistical precision and sensitivity of measures of dynamic gait stability.
Journal of neuroscience methods 178, 327–333 (2009).
64. Lockhart, T. & Liu, J. Differentiating fall-prone and healthy adults using local dynamic stability. Ergonomics 51, 1860–1872 (2008).
65. Myers, S. A. et al. Gait variability is altered in patients with peripheral arterial disease. J Vasc Surg 49, 924–931 (2009).
66. Vilhena de Mendonca, G. & Pereira, F. D. Between-day variability of net and gross oxygen uptake during graded treadmill walking:
effects of different walking intensities on the reliability of locomotion economy. Applied physiology, nutrition, and metabolism =
Physiologie appliquee, nutrition et metabolisme 33, 1199–1206, doi: 10.1139/h08-109 (2008).
Acknowledgements
We would like to thank Mads Rosenkilde, Department of Biomedical Sciences, University of Copenhagen and
Jesper Lundby-Jensen, Department of Nutrition, Exercise and Sports, University of Copenhagen for the use of
their oxygen uptake equipment. We would also like to thank Vaisakh Puthusserypady for the final-proof reading
of the manuscript. We sincerely thank the reviewers for their valuable suggestions.
Author Contributions
P.C.R., M.K.G., A.N.N. and T.A. designed and performed and the experiment. P.C.R., M.K.G., A.N.N., S.P. and
T.A. analysed and interpreted the results. P.C.R., S.P. and T.A. drafted the manuscript and all authors approved the
final version. All experiments were performed at the University of Copenhagen.
Additional Information
Supplementary information accompanies this paper at http://www.nature.com/srep
Competing Interests: The authors declare no competing financial interests.
How to cite this article: Raffalt, P. C. et al. Economy, Movement Dynamics, and Muscle Activity of Human
Walking at Different Speeds. Sci. Rep. 7, 43986; doi: 10.1038/srep43986 (2017).
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