Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2018 Sep 1.
Published in final edited form as: IEEE Trans Neural Syst Rehabil Eng. 2017 Apr 18;25(9):1612–1621. doi: 10.1109/TNSRE.2017.2683488

Biofeedback for gait retraining based on real-time estimation of tibiofemoral joint contact forces

C Pizzolato 1, M Reggiani 2, DJ Saxby 3, E Ceseracciu 4, L Modenese 5, DG Lloyd 6
PMCID: PMC5757380  NIHMSID: NIHMS905574  PMID: 28436878

Abstract

Biofeedback assisted rehabilitation and intervention technologies have the potential to modify clinically relevant biomechanics. Gait retraining has been used to reduce the knee adduction moment, a surrogate of medial tibiofemoral joint loading often used in knee osteoarthritis research. In this study we present an electromyogram-driven neuromusculoskeletal model of the lower-limb to estimate, in real-time, the tibiofemoral joint loads. The model included 34 musculotendon units spanning the hip, knee, and ankle joints. Full-body inverse kinematics, inverse dynamics, and musculotendon kinematics were solved in real-time from motion capture and force plate data to estimate the knee medial tibiofemoral contact force (MTFF). We analyzed 5 healthy subjects while they were walking on an instrumented treadmill with visual biofeedback of their MTFF. Each subject was asked to modify their gait in order to vary the magnitude of their MTFF. All subjects were able to increase their MTFF, whereas only 3 subjects could decrease it, and only after receiving verbal suggestions about possible gait modification strategies. Results indicate the important role of knee muscle activation patterns in modulating the MTFF. While this study focused on the knee, the technology can be extended to examine the musculoskeletal tissue loads at different sites of the human body.

Index Terms: Gait modification, real-time biofeedback, electromyography, knee joint, contact force

I. Introduction

INAPPROPRIATE loading to the medial tibiofemoral joint during walking is believed to be a main mechanical contributor to development and progression of medial compartment knee osteoarthritis (OA) [1]. Medial tibiofemoral contact force (MTFF) is due to a combination of externally applied knee loads [2, 3] and muscles forces [2, 46]. Increased external knee adduction moment (KAM), which is related to increased MTFF [7], has been associated with fast progression of medial knee OA [8], development of chronic knee pain [9], progression of articular tissue pathologies [10], and poor outcomes after high tibial osteotomy surgery [2, 11]. Conversely, muscle atrophy, known to reduce maximum muscle force production [12], is also associated with tissue-induced damage in animal knee OA [13, 14] and fast progression to knee OA [15]. These results implicate impaired muscle action in the pathogenesis of knee OA—although it is not yet known how it may affect MTFF.

There is an evolving understanding that MTFF underloading, in addition to overloading, may also be an important factor in the onset and progression of knee OA. Saxby and colleagues [16] have recently shown that at 2-year post anterior cruciate ligament reconstruction (ACLR) the MTFF are lower during walking, running, and side stepping compared to healthy controls. Additionally, healthy controls and ACLR without meniscal damage that have larger MTFF during walking have healthier cartilage and bone [17], while lower loading of MTFF at 2-year after ACLR may lead to greater risk of future onset of radiographic knee OA [18]. Currently it is unclear whether increasing or decreasing MTFF may offer therapeutic benefit; however, modifying gait to decrease MTFF has been proposed to slow the disease progression in those with established knee OA [1923].

Different gait strategies have been proposed to reduce the MTFF [22, 2427]. However, as the MTFF cannot be measured in-vivo in native knees, the KAM has commonly been used as a surrogate measure [7, 28]. The KAM during walking can be modified through kinematic changes [29], such as walking with toes pointed in [30, 31] or out [31, 32], increasing or decreasing side-to-side trunk sway [31, 33], using longer or shorter strides [31, 34], loading the inside or outside of the foot [34], changing the step width [35, 36], and changing the knee alignment [25, 37, 38]. Although gait retraining that uses biofeedback has been shown to successfully reduce the KAM [19, 21, 23, 38], is the KAM the correct biofeedback variable to manipulate MTFF?

The KAM has been positively correlated with the shape of MTFF during walking [7, 39], but this is not always the case [3, 4, 37, 40]. Studies based on instrumented tibiofemoral prostheses [41] have shown that decreases in the KAM do not necessarily result in decreases to MTFF [37], and that only small changes occurred in the MTFF for gait patterns designed 1to reduce KAM [42]. The KAM-MTFF relationship probably breaks down due to large muscular contributions to MTFF that are similar in magnitude to the contributions from external loads [4, 6]. Thus, it is essential to consider both external joint moments and muscle forces in order to estimate MTFF accurately [4, 6].

OpenSim [43] is a popular musculoskeletal modelling software for the analysis of the human motion that can account for individual variations in anatomy and movement [44]. However, OpenSim estimates muscle forces via optimisation-based algorithms (e.g. static and dynamic optimization) [45] that cannot account for alterations in muscle excitation patterns evident in individuals with knee pathologies during gait [46]. Alternatively to optimization-based methods, electromyogram (EMG)-driven neuromusculoskeletal (NMS) models [47] use experimentally measured muscle excitations to estimate muscle forces, and have been able to correctly predict MTFF and lateral knee contact force (LTFF) measured directly from instrumented knee implants [41, 48, 49].

In this study, a calibrated EMG-informed NMS model, i.e. CEINMS [50], was used in combination with OpenSim to estimate MTFF in real-time. Subjects were asked to modify their gait pattern in order to modify the model estimate of MTFF which was provided as visual biofeedback. Because of the novel approach, it was unclear whether subjects using this technology would be able to modify their gait strategy in order to manipulate their MTFF on-demand or if they would require suggestions. Also, it was unclear how subjects would change their gait strategy to alter their MTFF and if a common preferred strategy would emerge across the different subjects.

The aims of this paper were (1) developing a software based on both OpenSim and CEINMS to estimate knee contact forces in real-time using musculoskeletal modelling techniques, (2) comparing real-time and offline estimates, and (3) exploring the use of musculoskeletal tissue loading as visual biofeedback for gait retraining by evaluating the response of 5 different subjects in distinct experimental conditions.

II. Methods

A. Experimental setup

The Griffith University Human Research Ethics Committee approved the study and 5 healthy male participants (mass: 76.4 ± 6.4 kg, height: 1.78 ± 0.04 m, age: 26.8 ± 2.9 years) gave their written informed consent prior to testing. A 12-camera Vicon motion capture system (Oxford, UK) and an instrumented split-belt treadmill (Bertec Corporation, Columbus, OH, USA) were used to collect marker trajectories (200 Hz) from 44 retro-reflective markers [51] and ground reaction forces (GRF) (1000 Hz) in real-time. Surface EMGs (Zerowire, Milan, IT) were acquired (2000 Hz) from 16 site s on a single leg [52]: gluteus maximus, gluteus medius, tensor fasciae latae, rectus femoris, sartorius, vastus lateralis, vastus medialis, adductor group, gracilis, bicep femoris, semitendinosus, gastrocnemius medialis, gastrocnemius lateralis, soleus, tibialis anterioris, and peroneus group. The EMGs were mapped to 32 muscle tendon units (MTUs), as described in [53]. Muscle excitations were amplitude-normalized using a set of maximum isometric voluntary contractions (MVC) performed on a dynamometer (Biodex Medical Systems, Shirley, NY, USA). MVC for muscles crossing knee and ankle were acquired with subjects in a seated position at approximately 80 deg hip flexion, 60 deg knee flexion, and 0 deg ankle plantarflexion; MVC trials for muscles crossing the hip were first acquired in standing position, with the instrumented leg at 30 deg hip abduction, 0 deg for both knee flexion and ankle plantarflexion; and then in supine position at 60 deg hip flexion, 90 deg knee flexion and 0 deg ankle plantarflexion. The real-time data processing was executed on a Dell Precision Workstation T7500, with 2 Intel®Xeon®Processors X5660 (12 MB Cache, 2.80 GHz, 6 cores per processor), 8 GB of RAM, and Linux (kernel 4.2.0-18).

B. Software description

We developed software (C++) based on CEINMS [50] and OpenSim [43, 51] that uses a marker-based Vicon motion capture system, force plates, and EMG to estimate MTFF in real-time (Fig. 1). The MTFF was displayed on a screen to provide augmented visual sensory feedback to the subject walking on the treadmill. The software has five different components: (1) anatomical model, (2) real-time estimation of joint angles and moments [51], (3) real-time estimation of tibiofemoral contact forces, (4) musculotendon parameter calibration, and (5) biofeedback visualization. These are briefly described below.

Fig. 1.

Fig. 1

Schematic representation of the real-time system. Experimental data are synchronized in Vicon Nexus and streamed to the real-time pipeline. An anatomical model scaled to the subject is used to estimate joint angles and moments using real-time inverse kinematics and inverse dynamics, respectively. Joint angles and moments, as well as experimental EMG are used as input for CEINMS in order to estimate MTFF and LTFF. Data are then visualized in real-time on a custom graphic user interface (GUI).

C. The anatomical model

The generic gait2392 OpenSim model [43] was first modified to allow calculation of external adduction/abduction moments about lateral and medial condyle contact points [40] and then scaled to fit the anthropometry of each participant. The hip joint centers were calculated using regression equations [54], while knee and ankle joint centers were calculated from markers on the femoral epicondyles and ankle malleoli, respectively. Hip, knee, and ankle joint centers were then used to scale the anatomical model to the individual’s segments lengths using the OpenSim scale tool. The tibiofemoral intercondylar distances were scaled proportionally to femoral epicondyles distance [5, 6]. Further personalization of MTU insertion points and muscle paths was not performed. In the scaled anatomical model, tendon slack length and optimal fiber length of each MTU were estimated using the anthropometric scaling method developed by Modenese and colleagues [55].

D. Real-time estimation of joint angles and moments

Vicon Nexus software automatically reconstructed and labelled markers in real-time. Joint angles and moments were estimated through OpenSim’s inverse kinematics and inverse dynamics algorithms (Fig. 1). A state-space filter implementation of a 2nd order low-pass Butterworth filter [56], with a cut-off frequency of 15 Hz [51], was used to filter both the GRFs and joint angles. An extended description is provided in [51].

E. Real-time estimation of tibiofemoral contact forces

The tibiofemoral contact forces were estimated via CEINMS [50] in EMG-driven mode [47, 53]. This required, as inputs, MTU kinematics and muscle excitations. Multidimensional cubic B-splines, predefined using the OpenSim muscle analysis tool, calculated the MTU kinematics as a function of the joint angles [57] in real-time. Muscle excitations were calculated in real-time from raw EMGs that were high-pass filtered (30Hz), full-wave-rectified, low-pass filtered (6Hz) using a state-space 2nd order Butterworth filter [47, 56], and amplitude-normalized using the maximal values extracted from MVC trials acquired offline previously. Medial (FMC) and lateral (FLC) tibiofemoral contact forces were calculated as follows [6],

FMC=MMTULCMextLCdIC,FLC=MMTUMCMextMCdIC (1)

with,

MMTULC=inFMTUirMTUiLCand
MMTUMC=inFMTUirMTUiMC (2)

Where n represents the number of MTU crossing the knee joint, FMTUi the force exerted by the ith MTU, rMTUiLC and rMTUiMC the moment arm of the ith MTU about the lateral and medial condyle contact points, respectively, dIC the inter-condylar distance, and MMTULC/MMTUMC and MextLC/MextMC the net internal and external adduction/abduction moments about the lateral/medial condyle contact points, respectively. The n MTUs considered in the calculations were: bicep femoris long head, bicep femoris short head, semimembranosus, semitendinosus, gracilis, sartorius, rectus femoris, vastus medialis, vastus lateralis, vastus intermedius, gastrocnemius medialis, and gastrocnemius lateralis.

F. Model calibration

Prior to real-time capability, each participant’s MTU parameters were calibrated using CEINMS [50]. The CEINMS calibration is an offline procedure whereby the MTU parameters are optimized to minimize the summed square error between predicted and experimental joint moments whilst minimizing the peak magnitude of both MTFF and LTFF [48]. The calibration was performed using a set of 3 walking stance phases recorded and processed offline [58] before starting the real-time protocol. The list of calibrating parameters and boundary conditions is the same used in [50]. The total time for initial data collection, offline data processing and calibration was approximately 1.5 hours. After calibration, the system was ready to estimate the contact forces in real-time.

G. Biofeedback visualization

The real-time estimated MTFF was visualized as a continuous time series graph plotted on a screen placed in front of the subject (Fig. 2). Each new point was added to the rightmost part of the visualization window scrolling of previous data points to the left, and permitted visualization of the last 10 seconds of data (blue line in Fig. 2). The target was calculated as percentage of the moving average of the previous 15 medial contact force peaks and was also plotted onto the graph (red line in Fig. 2). This feedback modality was chosen to guide and promote the subject to further decrease or increase their MTFF.

Fig. 2.

Fig. 2

Visual feedback provided to the subject. The MTFF force is plotted in blue, with the current value at the right most point of the graph and a history of 2000 number data points remains. The moving average is plotted in red and superimposed on the graph.

H. Experimental protocol

Participants were given a period of familiarization with the treadmill and asked to select their preferred walking speed, which was maintained for the remainder of the session. The real-time protocol consisted of five different walking conditions. First, “baseline walking” was recorded for 1 minute and the mean of the peak values of MTFF was subsequently calculated. The subjects were then provided with the visual feedback of their MTFF and a target equal to 90% of the moving average of their MTFF peak. Subjects were then asked to decrease their MTFF driving the displayed value below the target (“decrease” condition). The subjects were then asked to try different strategies while trying to maintain a symmetric gait pattern; however in this instance specific instructions were not provided. The researchers verbally confirmed whether the strategy of the subjects was being effective or not when compared to their baseline level. When subjects found an effective gait strategy for reducing MTFF, they were asked to sustain it for 1 minute. Then a washout period of 5 minutes of normal walking was performed. Following washout, the same protocol was repeated asking the subjects to increase the medial force, using a target of 110% of MTFF peak displayed on screen (“increase” condition). After these self-guided gait trials, a washout period of 5 minutes of normal walking was performed, and then began a series of researcher-suggest gait pattern. The subjects were asked to decrease and then to increase their MTFF following the same protocol described above.

However, this time specific verbal suggestions were provided, which we refer to as “decrease with suggestions” and “increase with suggestions” conditions. The following gait strategies, previously found to modify external knee loading [31, 34, 59], were presented to the subjects in both the “decrease with suggestions” and “increase with suggestions” conditions: walking with toes pointed in [30, 31] or out [31, 32], increasing or decreasing side-to-side trunk sway [31, 33], using longer or shorter strides [31, 34], loading the inside or outside of the foot [34], changing the step width [35, 36], and changing the knee alignment [25, 37, 38], i.e. more medial or lateral knee positioning. Importantly, the suggested gait modifications were used as guidance to subject in order to find more effective gait modification strategies, but were not imposed.

I. Data analysis

a) Verification of real-time estimated contact forces

The MTFF and LTFF estimated offline and in real-time during walking trials were compared in order to verify the real-time system. A cross-correlation analysis between offline and real-time contact forces was used to estimate the time delays introduced by the state-space filters used in the real-time process. Then, real-time contact forces were time-shifted according to the delay, creating a time-aligned real-time data set. Offline, real-time, and time-aligned real-time contact forces were then divided into the repeated gait cycles. Root mean square errors (RMSE) were calculated between the offline and time-aligned real-time contact forces to reflect the error in time varying contact forces magnitude. For each gait cycle, real-time and offline MTFF and LTFF peak values were identified and a Bland-Altman analysis [60] was used to evaluate agreement. For each subject, representative curves were created using mean and standard deviation across time-normalized gait cycles. Average computation times were estimated via software using the std∷chrono∷system_clock class available in C++11.

b) Evaluation of gait modification protocol

For each subject, 1 minute of steady-state data from the five different protocol conditions were analyzed in order to evaluate (1) whether subjects were able to modify their MTFF from baseline with or without suggestions, and (2) how the change was achieved. For each gait cycle, the time frame corresponding to the MTFF peak was used to identify 12 dependent variables that are affected by the verbal suggestions: LTFF, trunk sway, stride length, step width (calculated as lateral distance between calcaneus markers at subsequent heel strikes), hip internal rotation, knee flexion angle, knee flexion moment, knee adduction moment, the external load contribution to the medial force, the MTU contribution to the medial force, the mean activation of the MTUs surrounding the knee, and the directed co-contraction ratio (DCCR) calculated from knee muscle activations [6, 46]:

DCCR={1Actext/Actflex,if Actflex>ActextActflex/Actext1,otherwise (3)

where Actext and Actflex are the mean activation of the knee extensors and flexors, respectively. For each variable, multiple paired t-tests were used to compare each condition to baseline. Finally, examples of how subjects searched for an optimal strategy in order to increase or decrease their MTFF were reported.

III. Results

The estimation of the MTFF was similar in real-time and offline, with an average (mean ± standard deviation) time-aligned RMSE of 0.125±0.069 BW and a time delay of 37.7±1.1 ms (Table I and Fig. 3). Differences between real-time and offline estimation of LTFF were larger, resulting in an average time-aligned RMSE of 0.192±0.60 BW and a time delay of 63.3±16.5 ms (Table I and Fig. 3). The Bland-Altman analysis (Fig. 4) reported a bias of 2.30% and agreement limits of −3.36 and 7.95% for the MTFF, and a bias of 16.13% and agreement limits of −1.32 and 33.59% for the LTFF.

TABLE I.

Medial tibiofemoral contact force
Time delay (ms) RMSE (BW) Time-adjusted RMSE (BW) Peak absolute error (BW)
SD SD SD
Subject 1 36.40 0.195 0.016 0.055 0.006 0.029 0.022
Subject 2 37.70 0.259 0.101 0.137 0.112 0.067 0.045
Subject 3 37.20 0.244 0.028 0.116 0.023 0.076 0.042
Subject 4 37.60 0.200 0.015 0.087 0.010 0.029 0.023
Subject 5 39.60 0.225 0.023 0.117 0.019 0.041 0.032

Average 37.70 0.226 0.056 0.125 0.069 0.049 0.040

Lateral tibiofemoral contact force
Time delay (ms) RMSE (BW) Time-adjusted RMSE (BW) Peak absolute error (BW)
SD SD SD

Subject 1 63.10 0.296 0.010 0.199 0.009 0.307 0.057
Subject 2 44.30 0.172 0.096 0.125 0.098 0.092 0.054
Subject 3 70.00 0.248 0.018 0.168 0.015 0.105 0.042
Subject 4 48.70 0.211 0.017 0.167 0.017 0.209 0.073
Subject 5 90.40 0.360 0.022 0.239 0.025 0.191 0.088

Average 63.30 0.258 0.081 0.192 0.600 0.178 0.101

Errors between real-time and offline, and time-adjusted real-time and offline predictions of MTFF and LTFF from 50 consecutive gait cycles for each subject. For each subject, time delays were calculated from a cross-correlation analysis performed on the entire data to avoid errors introduced by the uncertainties in the identification of different gait cycles. RMSE = Root Mean Square Error, BW = body weight, SD = standard deviation

Fig. 3.

Fig. 3

Comparison between tibiofemoral contact forces predicted offline (solid blue) and in real-time (dashed red) for 5 different subjects. For each subject, medial and lateral tibiofemoral contact forces from 50 consecutive gait cycles of baseline trials were normalized to body weight (BW), time normalized, and averaged to create representative mean curves. The blue and red points represent the maximum mean value of offline and real-time tibiofemoral contact forces, respectively. Shaded area represents ±1 standard deviation.

Fig. 4.

Fig. 4

Bland-Altman plot representing the agreement between real-time and offline estimations of MTFF and LTFF peaks from 50 consecutive gait cycle for baseline trials from all subjects.

The total time delay introduced by the real-time computation was approximately 115 ms. This included 4 ms of data processing in Vicon Nexus, 57 ms to calculate contact forces (including inverse kinematics, inverse dynamics, MTU kinematics, filtering, and muscle force estimation), 37 ms of time delay caused by the filtering phase shift (Table I), and 17 ms of refresh time of the 60 Hz monitor used to provide the visual biofeedback.

No subjects were able to decrease their MTFF without suggestions, but three subjects significantly decreased it following suggestions (Table II). All of the subjects were able to increase the MTFF, where for subjects 1, 2, and 3, the greatest change occurred after being provided suggestions. Fig. 5 summarizes the results across subjects and conditions and Fig. 6 shows examples of strategy search to decrease and increase MTFF.

TABLE II.

Percentage variation of peak MTFF from baseline
Decrease Decrease with suggestions Increase Increase with suggestions
±CI ±CI ±CI ±CI
Subject 1 2.31 1.72 3.88 2.05 4.85 2.54 20.79 2.83
Subject 2 −3.08 2.89 9.78 2.01 8.59 2.42 54.26 13.55
Subject 3 −0.91 2.88 26.77 2.68 6.93 1.76 18.70 2.36
Subject 4 0.70 1.66 3.15 1.68 136.05 16.32 31.61 4.52
Subject 5 −0.46 2.31 25.411 3.50 55.00 6.61 13.65 1.49

Percentage variation of peak LTFF from baseline
Decrease Decrease with suggestions Increase Increase with suggestions
±CI ±CI ±CI ±CI

Subject 1 0.26 1.86 21.88 2.42 9.88 2.30 16.53 2.48
Subject 2 22.78 10.09 28.56 7.12 28.97 7.12 45.73 14.25
Subject 3 15.45 2.61 13.55 5.72 34.27 2.45 28.29 1.97
Subject 4 27.71 9.44 −1.01 9.10 925.27 103.70 12.22 11.66
Subject 5 43.39 10.31 −1.37 4.08 34.40 18.39 13.65 3.24

Percentage variation of MTFF and LTFF across subjects and conditions. For each of the final steady-state conditions, the MTFF peak was calculated for each gait cycle. The time points corresponding to the peaks of the MTFF were then used to analyse LTFF. Bold font represents represents significant differences (p<0.05÷4, i.e. with Bonferroni correction) from baseline,

symbol represents significant differences for variation of MTFF opposite to the desired condition.

Fig. 5.

Fig. 5

Comparison among different subjects and different conditions across a variety of kinematic, kinetic, and muscle tendon force variables. For each of the final steady-state conditions, the MTFF peak was calculated for each gait cycle. The time points corresponding to the peaks of the MTFF were then used to analyse a variety of spatiotemporal, kinematic, kinetic, and muscular variables. The symbol ‘∗’ represents significant differences (p<0.05÷4, i.e. with Bonferroni correction) from baseline. Error bars indicate 95% confidence intervals

Fig. 6.

Fig. 6

A representative example of a strategy search to (a.) decrease MTFF (Subject 2, “decrease with suggestions” condition), and (b.) increase MTFF (Subject 4, “increase” condition). For each MTFF peak percentage variations from baseline were plotted as bar charts. High values for changes in DCCR (b.) were caused by baseline values close to zero. The red shaded area represents ±1 standard deviation of MTFF peaks from 50 consecutive gait cycle of baseline trials

IV. Discussion

We estimated MTFF and LTFF in real-time at 200 Hz, using a scaled OpenSim model and CEINMS in EMG-driven mode [50, 53]. EMG-driven NMS models have been previously used to estimate, in real-time, the MTU forces spanning knee and ankle [61, 62]. However, this is the first time they have been used to estimate, in real-time, articular loading from motion capture data. The real-time estimated MTFF was used as visual biofeedback to explore whether healthy individuals could modify their gait patterns to manipulate their MTFF. All subjects were able to increase their MTFF, whereas three subjects were able to decrease the MTFF after being provided with suggestions on how to change their gait patterns (Fig. 5 and Table II).

Differences between real-time and offline tibiofemoral estimates were limited, although larger errors were present in the real-time LTFF when compared to offline estimation (Table I and Fig. 3). Errors were caused by the combined effect of signal distortions associated with the real-time filtering of force plates, EMG, and kinematics data [51, 63]. Also, muscle forces contribute more to LTFF than MTFF [6], thus explaining larger errors (Table I and Fig. 3) and the inter-subject variability evident in the Bland-Altman analysis (Fig. 4).

As measuring knee contact forces in-vivo is challenging, direct validation of real-time estimated MTFF on healthy subjects using direct experimental measures was not performed. Offline estimation of MTFF using CEINMS was previously validated in [48] using data from instrumented knee implants [41]. Despite the differences between instrumented knee implants and healthy knees, CEINMS accounts for personalized excitation patterns and the OpenSim anatomical model can be adjusted to include variations in knee geometry and alignment [44, 48]. Thus, we considered CEINMS estimations of internal forces to be valid also on healthy subjects, and the offline CEINMS estimates of MTFF were used as the criteria for real-time verification in this study (Table I, Fig. 3, and Fig. 4). Some subjects presented values of MTFF that were higher in the first peak than second peak for their baseline gait (Fig. 3). However, variability in MTFF across subjects has been shown using instrumented knee implants [39], so it is not surprising to observe such variability in healthy individuals as well.

It could be argued that multiple gait strategy could be first tested in laboratory and then analyzed offline to identify the best strategy to manipulate MTFF. While this is possible, subjects may not be able to replicate novel gait patterns across sessions, or may find a combination of strategies more successful than a single strategy or more suited to their personal walking style. Also, while our study focused only on increasing and decreasing MTFF, specific MTFF values could be used as biofeedback target, which could be extremely difficult, or impossible, to perform offline.

The association between action and biofeedback improves as the biofeedback delay decreases [64]. Subjects were able to visualize the MTFF biofeedback as a continuous time series graph with a total delay of 115 ms from the data measurement. While the time delay of our system may not be optimal (i.e. less than 70 ms [64]), it was considered an improvement from visualizing the MTFF peak only, which would require to complete the current gait cycle before visualizing the new value [34], thus introducing a larger delay.

While previous gait retraining studies have used kinematic [23, 38, 65] and kinetic [21, 23] variables as biofeedback, we used the MTFF. The MTFF arises due to the complex changes in and interactions between whole-body kinematics, kinetics, and muscle coordination. No subject achieved a MTFF reduction when provided with only verbal and visual biofeedback, and the three subjects that did reduce their walking MTFF only did so when suggestions were given on gait modification strategies. Studies on individuals with instrumented implants also showed that alternative gait patterns did not lead to statistical significant reductions of MTFF [42], or that magnitude reductions were present in the second MTFF peak only [24, 37]. Interestingly, in the “decrease with suggestion” condition, subjects 1 and 5 were unable to decrease their MTFF lower than baseline (Table II and Fig. 5) and adopted altered gait that had the opposite effect, resulting in increased MTFF (Table II and Fig. 5). This may be a reflection of the study design and the subjects may have felt necessary to follow some of the provided suggestions even if they resulted in increased MTFF. Given the complex nature of the biofeedback, it is also plausible that subjects were unable to associate their action to the visual biofeedback. However, all subjects increased their MTFF, even without suggestions, indicating that a correct association between action and visual biofeedback was present. The inability of the subjects to reduce the MTFF without suggestions could be related to the visual biofeedback target magnitude, which was calculated from the peak of the MTFF of 15 previous gait cycles. Future studies investigating MTFF biofeedback should also consider evaluating what type of visual biofeedback (e.g. continuous time series, peaks, bars) works best, similarly to what has been done with KAM biofeedback [23, 29]. Finally, learning effects of the decrease strategy in the increase conditions cannot be excluded, as conditions were not randomized.

Gait strategies to modify the MTFF differed across subjects (Fig. 5). Previous gait retraining studies identified increased step width, medial knee thrust, increased hip internal rotation, and trunk sway as common strategies to decrease KAM [22, 66], even though large variations among subjects were reported [26, 27]. However, our model included joint kinematics, kinetics (e.g. KAM), and EMG-based MTU forces when estimating the MTFF. Since muscle activation patterns differ across tasks [67] and individuals even when the joint kinematics and kinetics are the same [68, 69], MTFF modulation strategies were expected to be different between different individuals. When using a large number of subjects, common kinematic patterns related to MTFF variations will likely emerge, but large variations would still be expected in the final strategies that individuals adopt.

A combination of kinematic, kinetic, and muscle activation changes were used by the subjects to manipulate their MTFF (Fig. 5). In the “decrease with suggestion” condition, subject 2 increased trunk sway and decreased hip internal rotation as their effective MTFF reduction strategy (Fig. 5 and Fig. 6). Interestingly, in the “increase” condition, subject 2 increased their MTFF (Fig. 5) by increasing their total muscle co-contraction, but maintained consistent KAM and knee flexion moment. Conversely, subject 4 used a different gait strategy to successfully increase MTFF by combining changes in stride length, hip internal rotation, knee flexion angle, trunk sway, and muscle activations and co-contraction (Fig. 5 and Fig. 6). Interestingly, subject 4 increased their MTFF by substantially increasing their total muscle activation, but reduced external loading with reduced KAM and knee flexion moment. Importantly, the use of the EMG-driven neural control solution in our NMS model was essential to identify changes in muscle forces due to variation in activation patterns and co-contraction, which static optimization based methods cannot correctly predict [70].

In this preliminary analysis, a reduction of MTFF did not always result in an increase of LTFF or vice-versa (Table II). However, LTFF results should be interpreted cautiously, as larger limits of agreement and bias are present in the LTFF estimates when compared to MTFF (Fig. 4). Also, variation in hip and ankle contact forces should be analyzed to better understand how variation in MTFF could affect other joints [71].

While this study aimed to evaluate whether the MTFF could be used for biofeedback, we recognize that subjects may struggle to adopt different kinematic patterns during gait, and that verbal suggestions may be essential to achieve MTFF reductions. Subjects were free to adopt any symmetrical gait pattern, but, as also observed by van den Noort and colleagues [23], this could result in extreme kinematics changes that are unsuitable for daily living activities. Furthermore, subjects were not allowed to walk with their new gait for a long period of time; thus, if they adopted a kinematic change, it is unlikely that they were walking with the most efficient coordination strategy [72]. Also, while multiple optimal solutions to decrease or increase MTFF may exist, subjects may have only explored a limited portion of the solution space. Computer simulations [25] and/or data-driven approaches [20] to suggest minimal gait kinematic changes could mitigate extreme gait patterns and address the limited time subject have to explore potential solutions.

This study has limitations that should be considered. Although scaled to the subjects’ dimensions and mass, the anatomical model was based on a generic template. This potentially produces less accurate estimates compared to subject-specific models [48]. Also, the inter-condyle distance in the knee model was scaled proportionally to the femoral epicondyles, possibly resulting in MTFF magnitude errors as the contact model is sensitive to the contact geometry [44, 49]. Further studies should include subject specific knee alignment [44], geometry [48], and kinematics [73] to improve the estimation of MTFF.

Prior using CEINMS in real-time, it was necessary to scale the anatomical model and calibrate the MTU parameters. These operations are time consuming, but they were performed within the same session to avoid marker and EMG electrode repositioning errors. To reduce the time burden on the subjects, we limited the CEINMS calibration time to less than 1 hour using the stance phase, rather than the full gait cycle. This potentially resulted in sub-optimal MTU parameters, although due to the complex solution space of the NMS system it is not at all clear that more calibration time will necessarily improve MTU parameter estimates. Future improvements will focus on the development of faster calibration routines able to operate “in the background” to automatically calibrate and updated MTU parameters during the real-time execution. Another limitation regards the use of the split-belt treadmill. The treadmill forced the subjects to maintain a minimum step width to avoid treading on the junction between the moving belts. Also, while the subjects were asked to maintain a symmetric gait, a measure of that symmetry was not provided as biofeedback. Thus, it is not possible to exclude compensatory changes in the contralateral limb, or in other joints. However, these should be considered in future clinical applications of this technology. Finally, while we acknowledge the listed limitations, we also stress the exploratory nature of this study and its main goal to assess whether people could use the MTFF as biofeedback to modify their gait.

V. Conclusions

This study presented the real-time estimation of MTFF and its use as a visual biofeedback variable for gait modification. The MTFF was estimated from joint angles and moments calculated through real-time inverse kinematics and inverse dynamics analyses, respectively, that were used within the CEINMS framework in EMG-driven mode [47, 50, 53]. The current study is not meant to be an extensive exploration of possible gait modification strategies, and further investigations into the use of MTFF for gait retraining involving a larger number of subjects is required before reaching general conclusions. Despite the modest sample size, these results show the importance of personalized NMS models that account for variations in movement, external joint loading, and muscle activation patterns across different individuals. Accounting for this variability is of particular importance when studying individuals with altered activation patterns [46, 74], joint pathology [75] or who have received specialized training [76]. Finally, the present research focused on the knee joint, yet the computational system is fully generic and could be applied to other musculoskeletal structures. While some limitations need to be addressed before translating this technology to clinical practice, merging real-time estimation of forces inside the human body with subject-specific anatomical models [77] can provide clinicians with accurate and relevant estimates of musculoskeletal loading, and has the potential to revolutionize the current use of post-hoc gait analysis for rehabilitation and training.

Acknowledgments

This work was supported by the Australian National Health and Medical Research Council (628850); the Royal Society of NZ Marsden Fund (12-UOA-1221); the US National Institutes of Health (R01EB009351); the EU-F7 Grant BioMot (project no. 611695); the Australian Research Council Linkage Project scheme (LP150100905); the Griffith University Areas of Strategic Investment Fund; and PhD scholarship from Griffith University and Menzies Health Institute Queensland. Contribution by Luca Modenese was supported in part by the EPSRC under Grant EP/K03877X/1 and Grant FP7-ICT-600932;

Biographies

graphic file with name nihms905574b1.gif

Claudio Pizzolato received a M.Sc. degree in mechatronic engineering from the University of Padua, Italy, in 2011 and completed his Ph.D. in biomechanics at Griffith University, QLD, Australia, in 2016. Currently, he is a Post-Doctoral Research Fellow at the Menzies Health Institute Queensland, Griffith University, QLD, Australia.

graphic file with name nihms905574b2.gif

Monica Reggiani (M’98) received the Graduate and Ph.D. degrees in computer engineering from the University of Parma, Parma, Italy in 1997 and 2001, respectively. She is currently an Assistant Professor at the University of Padua, Italy. Her research interests include human–robot interfaces, motion planning, programming by demonstration, and autonomous robots.

graphic file with name nihms905574b3.gif

David J. Saxby was graduated from the University of Ottawa, Canada, (B.Sc. and M.Sc. Human Kinetics) and Griffith University, Australia (Ph.D. Biome-chanics). He is currently a researcher and lecturer at Griffith University, and his research focuses on computational modelling of articular loading during human gait and its effects on tissue health.

graphic file with name nihms905574b4.gif

Elena Ceseracciu holds a M.Sc. with honors (2007) and Ph.D. (2011) in Bioengineering, both from the University of Padua, Italy. Currently, she is a postdoc at the University of Padua within the BioMot European Project, working on improving exoskeleton technology for rehabilitation purposes.

graphic file with name nihms905574b5.gif

Luca Modenese received a M.Sc. degree in mechanical engineering (magna cum laude) from the University of Padua (2008) and completed his Ph.D. in biomechanics at Imperial College London in 2013. Luca is currently a postdoctoral researcher at the INSIGNEO Institute for in silico Medicine, University of Sheffield (UK).

graphic file with name nihms905574b6.gif

David G. Lloyd received the B.Sc. degree in mechanical engineering from the University of New South Wales, Sydney, Australia, in 1984. He received the Ph.D. degree in biomechanical engineering from the University of New South Wales, Sydney, NSW, Australia, in 1994, after working in industry for several years. He is currently a Professor at Griffith University, QLD, Australia.

Contributor Information

C. Pizzolato, School of Allied Health Sciences and Menzies Health Institute Queensland, Griffith University, Gold Coast, Australia

M. Reggiani, Department of Management and Engineering, University of Padua, Italy.

D.J. Saxby, School of Allied Health Sciences and Menzies Health Institute Queensland, Griffith University, Gold Coast, Australia

E. Ceseracciu, Department of Management and Engineering, University of Padua, Italy

L. Modenese, Department of Mechanical Engineering and INSIGNEO Institute for in silico Medicine, University of Sheffield, UK

D.G. Lloyd, School of Allied Health Sciences and Menzies Health Institute Queensland, Griffith University, Gold Coast, Australia

References

  • 1.Andriacchi TP, Mundermann A. The role of ambulatory mechanics in the initiation and progression of knee osteoarthritis. Current Opinion in Rheumatology. 2006 Sep;18(5):514–518. doi: 10.1097/01.bor.0000240365.16842.4e. [DOI] [PubMed] [Google Scholar]
  • 2.Prodromos CC, Andriacchi TP, Galante JO. A Relationship between Gait and Clinical Changes Following High Tibial Osteotomy. Journal of Bone and Joint Surgery-American Volume. 1985;67A(8):1188–1194. [PubMed] [Google Scholar]
  • 3.Manal K, Gardinier E, Buchanan TS, Snyder-Mackler L. A more informed evaluation of medial compartment loading: the combined use of the knee adduction and flexor moments. Osteoarthritis Cartilage. 2015 Jul;23(7):1107–11. doi: 10.1016/j.joca.2015.02.779. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Walter JP, Korkmaz N, Fregly BJ, Pandy MG. Contribution of tibiofemoral joint contact to net loads at the knee in gait. J Orthop Res. 2015 Jul;33(7):1054–60. doi: 10.1002/jor.22845. [DOI] [PubMed] [Google Scholar]
  • 5.Winby CR, Gerus P, Kirk TB, Lloyd DG. Correlation between EMG-based co-activation measures and medial and lateral compartment loads of the knee during gait. Clin Biomech (Bristol, Avon) 2013 Nov-Dec;28(9-10):1014–9. doi: 10.1016/j.clinbiomech.2013.09.006. [DOI] [PubMed] [Google Scholar]
  • 6.Winby CR, Lloyd DG, Besier TF, Kirk TB. Muscle and external load contribution to knee joint contact loads during normal gait. J Biomech. 2009 Oct 16;42(14):2294–300. doi: 10.1016/j.jbiomech.2009.06.019. [DOI] [PubMed] [Google Scholar]
  • 7.Zhao D, Banks SA, Mitchell KH, D’Lima DD, Colwell CW, Fregly BJ. Correlation between the knee adduction torque and medial contact force for a variety of gait patterns. Journal of Orthopaedic Research. 2007 Jun;25(6):789–797. doi: 10.1002/jor.20379. [DOI] [PubMed] [Google Scholar]
  • 8.Miyazaki T, Wada M, Kawahara H, Sato M, Baba H, Shimada S. Dynamic load at baseline can predict radiographic disease progression in medial compartment knee osteoarthritis. Annals of the Rheumatic Diseases. 2002 Jul;61(7):617–622. doi: 10.1136/ard.61.7.617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Amin S, Luepongsak N, McGibbon CA, LaValley MP, Krebs DE, Felson DT. Knee adduction moment and development of chronic knee pain in elders. Arthritis Rheum. 2004 Jun 15;51(3):371–6. doi: 10.1002/art.20396. [DOI] [PubMed] [Google Scholar]
  • 10.Bennell KL, Creaby MW, Wrigley TV, Bowles KA, Hinman RS, Cicuttini F, Hunter DJ. Bone marrow lesions are related to dynamic knee loading in medial knee osteoarthritis. Annals of the Rheumatic Diseases. 2010 Jun;69(6):1151–1154. doi: 10.1136/ard.2009.118182. [DOI] [PubMed] [Google Scholar]
  • 11.Wang JW, Kuo KN, Andriacchi TP, Galante JO. The Influence of Walking Mechanics and Time on the Results of Proximal Tibial Osteotomy. Journal of Bone and Joint Surgery-American Volume. 1990 Jul;72A(6):905–909. [PubMed] [Google Scholar]
  • 12.Narici MV, Hoppeler H, Kayser B, Landoni L, Claassen H, Gavardi C, Conti M, Cerretelli P. Human quadriceps cross-sectional area, torque and neural activation during 6 months strength training. Acta Physiol Scand. 1996 Jun;157(2):175–86. doi: 10.1046/j.1365-201X.1996.483230000.x. [DOI] [PubMed] [Google Scholar]
  • 13.Egloff C, Sawatsky A, Leonard T, Hart DA, Valderrabano V, Herzog W. Effect of muscle weakness and joint inflammation on the onset and progression of osteoarthritis in the rabbit knee. Osteoarthritis Cartilage. 2014 Nov;22(11):1886–93. doi: 10.1016/j.joca.2014.07.026. [DOI] [PubMed] [Google Scholar]
  • 14.Leumann A, Longino D, Fortuna R, Leonard T, Vaz MA, Hart DA, Herzog W. Altered cell metabolism in tissues of the knee joint in a rabbit model of Botulinum toxin A-induced quadriceps muscle weakness. Scand J Med Sci Sports. 2012 Dec;22(6):776–82. doi: 10.1111/j.1600-0838.2011.01309.x. [DOI] [PubMed] [Google Scholar]
  • 15.Wang Y, Wluka AE, Berry PA, Siew T, Teichtahl AJ, Urquhart DM, Lloyd DG, Jones G, Cicuttini FM. Increase in vastus medialis cross-sectional area is associated with reduced pain, cartilage loss, and joint replacement risk in knee osteoarthritis. Arthritis Rheum. 2012 Dec;64(12):3917–25. doi: 10.1002/art.34681. [DOI] [PubMed] [Google Scholar]
  • 16.Saxby DJ, Bryant AL, Modenese L, Gerus P, Killen BA, Kon-rath J, Fortin K, Wrigley TV, Bennell KL, Cicuttini FM, Vertullo C, Feller JA, Whitehead T, Gallie P, Lloyd DG. Tibiofemoral Contact Forces in the Anterior Cruciate Ligament-Reconstructed Knee. Med Sci Sports Exerc. 2016 Nov;48(11):2195–2206. doi: 10.1249/MSS.0000000000001021. [DOI] [PubMed] [Google Scholar]
  • 17.Saxby DJ, Wang X, Bryant AL, Modenese L, Gerus P, Konrath J, Fortin K, Wrigley TV, Bennell KL, Cicuttini FM, Vertullo C, Feller JA, Whitehead T, Gallie P, Lloyd DG. Tibiofemoral Contact Forces Protect against Articular Tissue Damage in the Anterior Cruciate Ligament Reconstructed Knee, but Not If There Is Concurent Meniscal Injury. Osteoarthritis and Cartilage. 2016 Apr;24:S94–S94. [Google Scholar]
  • 18.Wellsandt E, Gardinier ES, Manal K, Axe MJ, Buchanan TS, Snyder-Mackler L. Decreased Knee Joint Loading Associated With Early Knee Osteoarthritis After Anterior Cruciate Ligament Injury. Am J Sports Med. 2016 Jan;44(1):143–51. doi: 10.1177/0363546515608475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Dowling AV, Fisher DS, Andriacchi TP. Gait modification via verbal instruction and an active feedback system to reduce peak knee adduction moment. J Biomech Eng. 2010 Jul;132(7):071007. doi: 10.1115/1.4001584. [DOI] [PubMed] [Google Scholar]
  • 20.Shull PB, Lurie KL, Cutkosky MR, Besier TF. Training multi-parameter gaits to reduce the knee adduction moment with data-driven models and haptic feedback. J Biomech. 2011 May 17;44(8):1605–1609. doi: 10.1016/j.jbiomech.2011.03.016. [DOI] [PubMed] [Google Scholar]
  • 21.Shull PB, Silder A, Shultz R, Dragoo JL, Besier TF, Delp SL, Cutkosky MR. Six-week gait retraining program reduces knee adduction moment, reduces pain, and improves function for individuals with medial compartment knee osteoarthritis. J Orthop Res. 2013 Jul;31(7):1020–5. doi: 10.1002/jor.22340. [DOI] [PubMed] [Google Scholar]
  • 22.Simic M, Hinman RS, Wrigley TV, Bennell KL, Hunt MA. Gait modification strategies for altering medial knee joint load: a systematic review. Arthritis Care Res (Hoboken) 2011 Mar;63(3):405–26. doi: 10.1002/acr.20380. [DOI] [PubMed] [Google Scholar]
  • 23.van den Noort JC, Steenbrink F, Roeles S, Harlaar J. Real-time visual feedback for gait retraining: toward application in knee osteoarthritis. Med Biol Eng Comput. 2015 Mar;53(3):275–86. doi: 10.1007/s11517-014-1233-z. [DOI] [PubMed] [Google Scholar]
  • 24.Fregly BJ, D’Lima DD, Colwell CW., Jr Effective gait patterns for offloading the medial compartment of the knee. J Orthop Res. 2009 Aug;27(8):1016–21. doi: 10.1002/jor.20843. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Fregly BJ, Reinbolt JA, Rooney KL, Mitchell KH, Chmielewski TL. Design of patient-specific gait modifications for knee osteoarthritis rehabilitation. IEEE Trans Biomed Eng. 2007 Sep;54(9):1687–95. doi: 10.1109/TBME.2007.891934. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Mundermann A, Asay JL, Mundermann L, Andriacchi TP. Implications of increased medio-lateral trunk sway for ambulatory mechanics. J Biomech. 2008;41(1):165–170. doi: 10.1016/j.jbiomech.2007.07.001. [DOI] [PubMed] [Google Scholar]
  • 27.Chang A, Hurwitz D, Dunlop D, Song J, Cahue S, Hayes K, Sharma L. The relationship between toe-out angle during gait and progression of medial tibiofemoral osteoarthritis. Annals of the Rheumatic Diseases. 2007 Oct;66(10):1271–5. doi: 10.1136/ard.2006.062927. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Birmingham TB, Hunt MA, Jones IC, Jenkyn TR, Giffin JR. Test-retest reliability of the peak knee adduction moment during walking in patients with medial compartment knee osteoarthritis. Arthritis Rheum. 2007 Aug 15;57(6):1012–7. doi: 10.1002/art.22899. [DOI] [PubMed] [Google Scholar]
  • 29.Richards R, van den Noort JC, Dekker J, Harlaar J. Gait Retraining With Real-Time Biofeedback to Reduce Knee Adduction Moment: Systematic Review of Effects and Methods Used. Arch Phys Med Rehabil. 2017 Jan;98(1):137–150. doi: 10.1016/j.apmr.2016.07.006. [DOI] [PubMed] [Google Scholar]
  • 30.Shull PB, Shultz R, Silder A, Dragoo JL, Besier TF, Cutkosky MR, Delp SL. Toe-in gait reduces the first peak knee adduction moment in patients with medial compartment knee osteoarthritis. J Biomech. 2013 Jan 4;46(1):122–8. doi: 10.1016/j.jbiomech.2012.10.019. [DOI] [PubMed] [Google Scholar]
  • 31.van den Noort JC, Schaffers I, Snijders J, Harlaar J. The effectiveness of voluntary modifications of gait pattern to reduce the knee adduction moment. Hum Mov Sci. 2013 Jun;32(3):412–24. doi: 10.1016/j.humov.2012.02.009. [DOI] [PubMed] [Google Scholar]
  • 32.Guo M, Axe MJ, Manal K. The influence of foot progression angle on the knee adduction moment during walking and stair climbing in pain free individuals with knee osteoarthritis. Gait Posture. 2007 Sep;26(3):436–441. doi: 10.1016/j.gaitpost.2006.10.008. [DOI] [PubMed] [Google Scholar]
  • 33.Hunt MA, Birmingham TB, Bryant D, Jones I, Giffin JR, Jenkyn TR, Vandervoort AA. Lateral trunk lean explains variation in dynamic knee joint load in patients with medial compartment knee osteoarthritis. Osteoarthritis Cartilage. 2008 May;16(5):591–9. doi: 10.1016/j.joca.2007.10.017. [DOI] [PubMed] [Google Scholar]
  • 34.Wheeler JW, Shull PB, Besier TF. Real-time knee adduction moment feedback for gait retraining through visual and tactile displays. J Biomech Eng. 2011 Apr;133(4):041007–041007. doi: 10.1115/1.4003621. [DOI] [PubMed] [Google Scholar]
  • 35.Fregly BJ, Reinbolt JA, Chmielewski TL. Evaluation of a patient-specific cost function to predict the influence of foot path on the knee adduction torque during gait. Comput Methods Biomech Biomed Engin. 2008 Feb;11(1):63–71. doi: 10.1080/10255840701552036. [DOI] [PubMed] [Google Scholar]
  • 36.Street BD, Gage W. The effects of an adopted narrow gait on the external adduction moment at the knee joint during level walking: Evidence of asymmetry. Human Movement Science. 2013 Apr;32(2):301–313. doi: 10.1016/j.humov.2012.08.007. [DOI] [PubMed] [Google Scholar]
  • 37.Walter JP, D’Lima DD, Colwell CW, Jr, Fregly BJ. Decreased knee adduction moment does not guarantee decreased medial contact force during gait. J Orthop Res. 2010 Oct;28(10):1348–54. doi: 10.1002/jor.21142. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Barrios JA, Crossley KM, Davis IS. Gait retraining to reduce the knee adduction moment through real-time visual feedback of dynamic knee alignment. J Biomech. 2010 Aug 10;43(11):2208–13. doi: 10.1016/j.jbiomech.2010.03.040. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Kutzner I, Trepczynski A, Heller MO, Bergmann G. Knee adduction moment and medial contact force–facts about their correlation during gait. Plos One. 2013 Dec 2;8(12):e81036. doi: 10.1371/journal.pone.0081036. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Saxby DJ, Modenese L, Bryant AL, Gerus P, Killen B, Fortin K, Wrigley TV, Bennell KL, Cicuttini FM, Lloyd DG. Tibiofemoral contact forces during walking, running and sidestepping. Gait Posture. 2016 Sep;49:78–85. doi: 10.1016/j.gaitpost.2016.06.014. [DOI] [PubMed] [Google Scholar]
  • 41.Fregly BJ, Besier TF, Lloyd DG, Delp SL, Banks SA, Pandy MG, D’Lima DD. Grand challenge competition to predict in vivo knee loads. J Orthop Res. 2012 Apr;30(4):503–13. doi: 10.1002/jor.22023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Kinney AL, Besier TF, Silder A, Delp SL, D’Lima DD, Fregly BJ. Changes in in vivo knee contact forces through gait modification. J Orthop Res. 2013 Mar;31(3):434–40. doi: 10.1002/jor.22240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Delp SL, Anderson FC, Arnold AS, Loan P, Habib A, John CT, Guendelman E, Thelen DG. OpenSim: open-source software to create and analyze dynamic simulations of movement. IEEE Trans Biomed Eng. 2007 Nov;54(11):1940–50. doi: 10.1109/TBME.2007.901024. [DOI] [PubMed] [Google Scholar]
  • 44.Lerner ZF, DeMers MS, Delp SL, Browning RC. How tibiofemoral alignment and contact locations affect predictions of medial and lateral tibiofemoral contact forces. J Biomech. 2015 Feb 26;48(4):644–50. doi: 10.1016/j.jbiomech.2014.12.049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Anderson FC, Pandy MG. Static and dynamic optimization solutions for gait are practically equivalent. J Biomech. 2001 Feb;34(2):153–61. doi: 10.1016/s0021-9290(00)00155-x. [DOI] [PubMed] [Google Scholar]
  • 46.Heiden TL, Lloyd DG, Ackland TR. Knee joint kinematics, kinetics and muscle co-contraction in knee osteoarthritis patient gait. Clinical Biomechanics. 2009 Dec;24(10):833–841. doi: 10.1016/j.clinbiomech.2009.08.005. [DOI] [PubMed] [Google Scholar]
  • 47.Lloyd DG, Besier TF. An EMG-driven musculoskeletal model to estimate muscle forces and knee joint moments in vivo. J Biomech. 2003 Jun;36(6):765–76. doi: 10.1016/s0021-9290(03)00010-1. [DOI] [PubMed] [Google Scholar]
  • 48.Gerus P, Sartori M, Besier TF, Fregly BJ, Delp SL, Banks SA, Pandy MG, D’Lima DD, Lloyd DG. Subject-specific knee joint geometry improves predictions of medial tibiofemoral contact forces. J Biomech. 2013 Nov 15;46(16):2778–86. doi: 10.1016/j.jbiomech.2013.09.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Manal K, Buchanan TS. An electromyogram-driven muscu-loskeletal model of the knee to predict in vivo joint contact forces during normal and novel gait patterns. J Biomech Eng. 2013 Feb;135(2):021014. doi: 10.1115/1.4023457. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Pizzolato C, Lloyd DG, Sartori M, Ceseracciu E, Besier TF, Fregly BJ, Reggiani M. CEINMS: A toolbox to investigate the influence of different neural control solutions on the prediction of muscle excitation and joint moments during dynamic motor tasks. J Biomech. 2015 Nov 5;48(14):3929–36. doi: 10.1016/j.jbiomech.2015.09.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Pizzolato C, Reggiani M, Modenese L, Lloyd DG. Real-time inverse kinematics and inverse dynamics for lower limb applications using OpenSim. Comput Methods Biomech Biomed Engin. 2016 Oct 10;:1–10. doi: 10.1080/10255842.2016.1240789. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Hermens HJ, Freriks B, Disselhorst-Klug C, Rau G. Development of recommendations for SEMG sensors and sensor placement procedures. Journal of Electromyography and Kinesiology. 2000 Oct;10(5):361–374. doi: 10.1016/s1050-6411(00)00027-4. [DOI] [PubMed] [Google Scholar]
  • 53.Sartori M, Reggiani M, Farina D, Lloyd DG. EMG-driven forward-dynamic estimation of muscle force and joint moment about multiple degrees of freedom in the human lower extremity. Plos One. 2012;7(12):e52618. doi: 10.1371/journal.pone.0052618. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Harrington ME, Zavatsky AB, Lawson SE, Yuan Z, Theologis TN. Prediction of the hip joint centre in adults, children, and patients with cerebral palsy based on magnetic resonance imaging. J Biomech. 2007;40(3):595–602. doi: 10.1016/j.jbiomech.2006.02.003. [DOI] [PubMed] [Google Scholar]
  • 55.Modenese L, Ceseracciu E, Reggiani M, Lloyd DG. Estimation of musculotendon parameters for scaled and subject specific muscu-loskeletal models using an optimization technique. J Biomech. 2016 Jan 25;49(2):141–8. doi: 10.1016/j.jbiomech.2015.11.006. [DOI] [PubMed] [Google Scholar]
  • 56.van den Bogert AJ, Geijtenbeek T, Even-Zohar O, Steenbrink F, Hardin EC. A real-time system for biomechanical analysis of human movement and muscle function. Med Biol Eng Comput. 2013 Oct;51(10):1069–77. doi: 10.1007/s11517-013-1076-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Sartori M, Reggiani M, van den Bogert AJ, Lloyd DG. Estimation of musculotendon kinematics in large musculoskeletal models using multidimensional B-splines. J Biomech. 2012 Feb 2;45(3):595–601. doi: 10.1016/j.jbiomech.2011.10.040. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Mantoan A, Pizzolato C, Sartori M, Sawacha Z, Cobelli C, Reggiani M. MOtoNMS: A MATLAB toolbox to process motion data for neuromusculoskeletal modeling and simulation. Source Code Biol Med. 2015;10(1):12. doi: 10.1186/s13029-015-0044-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Fregly BJ. Gait modification to treat knee osteoarthritis. HSS J. 2012 Feb;8(1):45–8. doi: 10.1007/s11420-011-9229-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Bland JM, Altman DG. Statistical Methods for Assessing Agreement between Two Methods of Clinical Measurement. Lancet. 1986 Feb 8;1(8476):307–310. [PubMed] [Google Scholar]
  • 61.Ceseracciu E, Mantoan A, Bassa M, Moreno JC, Pons JL, Prieto GA, del Ama AJ, Marquez-Sanchez E, Gil-Agudo A, Pizzolato C, Lloyd DG, Reggiani M. A Flexible Architecture to Enhance Wearable Robots: Integration of EMG-informed Models. 2015 Ieee/Rsj International Conference on Intelligent Robots and Systems (Iros) 2015:4368–4374. Sept. 28 2015-Oct. 2 2015. [Google Scholar]
  • 62.Manal K, Gravare-Silbernagel K, Buchanan TS. A Real-time EMG-driven Musculoskeletal Model of the Ankle. Multibody Syst Dyn. 2012 Aug;28(1-2):169–180. doi: 10.1007/s11044-011-9285-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Manal K, Rose W. A general solution for the time delay introduced by a low-pass Butterworth digital filter: An application to musculoskeletal modeling. J Biomech. 2007;40(3):678–81. doi: 10.1016/j.jbiomech.2006.02.001. [DOI] [PubMed] [Google Scholar]
  • 64.Kannape OA, Blanke O. Self in motion: sensorimotor and cognitive mechanisms in gait agency. J Neurophysiol. 2013 Oct;110(8):1837–47. doi: 10.1152/jn.01042.2012. [DOI] [PubMed] [Google Scholar]
  • 65.Hunt MA, Simic M, Hinman RS, Bennell KL, Wrigley TV. Feasibility of a gait retraining strategy for reducing knee joint loading: increased trunk lean guided by real-time biofeedback. J Biomech. 2011 Mar 15;44(5):943–7. doi: 10.1016/j.jbiomech.2010.11.027. [DOI] [PubMed] [Google Scholar]
  • 66.Gerbrands TA, Pisters MF, Vanwanseele B. Individual selection of gait retraining strategies is essential to optimally reduce medial knee load during gait. Clin Biomech (Bristol, Avon) 2014 Aug;29(7):828–34. doi: 10.1016/j.clinbiomech.2014.05.005. [DOI] [PubMed] [Google Scholar]
  • 67.Buchanan TS, Shreeve DA. An evaluation of optimization techniques for the prediction of muscle activation patterns during isometric tasks. J Biomech Eng. 1996 Nov;118(4):565–74. doi: 10.1115/1.2796044. [DOI] [PubMed] [Google Scholar]
  • 68.Buchanan TS, Lloyd DG. Muscle-Activity Is Different for Humans Performing Static Tasks Which Require Force Control and Position Control. Neuroscience Letters. 1995 Jul 14;194(1-2):61–64. doi: 10.1016/0304-3940(95)11727-e. [DOI] [PubMed] [Google Scholar]
  • 69.Tax AA, Denier van der Gon JJ, Gielen CC, Kleyne M. Differences in central control of m. biceps brachii in movement tasks and force tasks. Experimental Brain Research. 1990;79(1):138–42. doi: 10.1007/BF00228882. [DOI] [PubMed] [Google Scholar]
  • 70.Lloyd DG, Buchanan TS. Strategies of muscular support of varus and valgus isometric loads at the human knee. J Biomech. 2001 Oct;34(10):1257–1267. doi: 10.1016/s0021-9290(01)00095-1. [DOI] [PubMed] [Google Scholar]
  • 71.DeMers MS, Pal S, Delp SL. Changes in Tibiofemoral Forces due to Variations in Muscle Activity during Walking. Journal of Orthopaedic Research. 2014 Jun;32(6):769–776. doi: 10.1002/jor.22601. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Caldwell LK, Laubach LL, Barrios JA. Effect of specific gait modifications on medial knee loading, metabolic cost and perception of task difficulty. Clinical Biomechanics. 2013 Jul;28(6):649–654. doi: 10.1016/j.clinbiomech.2013.05.012. [DOI] [PubMed] [Google Scholar]
  • 73.Brito da Luz S, Modenese L, Sancisi N, Mills PM, Kennedy B, Beck BR, Lloyd DG. Feasibility of using MRIs to create subject-specific parallel-mechanism joint models. Journal of Biomechanics. 2016 doi: 10.1016/j.jbiomech.2016.12.018. vol. In print. [DOI] [PubMed] [Google Scholar]
  • 74.Heiden TL, Lloyd DG, Ackland TR. Knee Extension and Flexion Weakness in People With Knee Osteoarthritis: Is Antagonist Cocontraction a Factor? Journal of Orthopaedic & Sports Physical Therapy. 2009 Nov;39(11):807–815. doi: 10.2519/jospt.2009.3079. [DOI] [PubMed] [Google Scholar]
  • 75.Besier TF, Fredericson M, Gold GE, Beaupré GS, Delp SL. Knee muscle forces during walking and running in patellofemoral pain patients and pain-free controls. Journal of biomechanics. 2009;42:898–905. doi: 10.1016/j.jbiomech.2009.01.032. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Menegaldo LL, Oliveira LF. An EMG-driven model to evaluate quadriceps strengthening after an isokinetic training. Iutam Symposium on Human Body Dynamics. 2011;2:131–141. [Google Scholar]
  • 77.Fregly BJ, Boninger ML, Reinkensmeyer DJ. Personalized neuromusculoskeletal modeling to improve treatment of mobility impairments: a perspective from European research sites. J Neuroeng Rehabil. 2012 Mar 30;9:18. doi: 10.1186/1743-0003-9-18. [DOI] [PMC free article] [PubMed] [Google Scholar]

RESOURCES