Seediscussions,stats,andauthorprofilesforthispublicationat:https://www.researchgate.net/publication/230780639 ComparisonofStrain-GageandFiber-Optic GoniometryforMeasuringKneeKinematics DuringActivitiesofDailyLivingandExercise ArticleinJournalofBiomechanicalEngineering·August2012 ImpactFactor:1.78·DOI:10.1115/1.4007094·Source:PubMed CITATIONS READS 6 150 6authors,including: AbeerMohamed AndrewSexton UniversityofNewBrunswick UniversityofNewBrunswick 2PUBLICATIONS6CITATIONS 11PUBLICATIONS11CITATIONS SEEPROFILE Allin-textreferencesunderlinedinbluearelinkedtopublicationsonResearchGate, lettingyouaccessandreadthemimmediately. SEEPROFILE Availablefrom:AndrewSexton Retrievedon:16May2016 Comparison of Strain-Gage and Fiber-Optic Goniometry for Measuring Knee Kinematics During Activities of Daily Living and Exercise The results indicate that both goniometers were within 2–5 degrees of the Vicon angles for gait and chair rise. For some deep knee bend trials, disagreement with Vicon angles exceeded ten degrees for both devices. We conclude that both goniometers can record ADL knee movement faithfully and accurately, but should be carefully considered when high (>120 deg) knee flexion angles are required. [DOI: 10.1115/1.4007094] Abeer A. Mohamed Keywords: knee kinematics, flexible goniometer, fiberoptic goniometry, gait, chair rise, deep knee bend Jennifer Baba 1 Institute of Biomedical Engineering and Department of Mechanical Engineering, University of New Brunswick, Fredericton, NB, E3B 5A3 Canada Introduction Rehabilitation following onset of knee joint disease, injury or surgery often requires assessment of mobility during common activity of daily living, such as walking or rising from a chair [1,2], or deep knee bends [3,4]. In these studies, highly sophisticated optical or radiographic systems were used to assess knee joint motion; however, this technology is not available to the majority of clinics, and costs of personnel, training and maintenance can be prohibitive even when such facilities are readily available. Wearable sensor technology offers a potential solution to this barrier [5] by enabling functional outcomes to be measured outside the laboratory or clinic. Recent focus has centered on inertial measurement devices for indirectly quantifying joint motion [6,7]. However, flexible goniometry can provide direct measurement of joint angle and is easily deployed in the field [8]. Flexible straingauge goniometers are portable and reliable [9,10] and remain popular in laboratory environments [8,11]. A common choice for the knee is the SG150 Penny & GilesTM goniometer (Biometrics Ltd, Gwent, UK; Figs. 1(a) and 1(c)) [8,12,13]. An alternative flexible goniometer is the S700 ShapeSensorTM fiber-optic goniometer (Measurand Inc. Fredericton, Canada; Figs. 1(b) and 1(c)). This device consists of a fiber-optic sensor embedded in a thin, flat and flexible vinyl casing joining the two end blocks. Although fiber-optic sensors have been use in rehabilitation and biomechanics applications [14], we know of no studies comparing these two different flexible goniometer devices. Therefore, the primary objective of this project was to evaluate the measurement error of both a strain-gauge goniometer (Penny & Giles Egon) and a fiber-optic goniometer (ShapeSensorTM, James Beyea Institute of Biomedical Engineering and Faculty of Kinesiology, University of New Brunswick, Fredericton, NB, E3B 5A3 Canada John Landry Andrew Sexton Institute of Biomedical Engineering, University of New Brunswick, Fredericton, NB, E3B 5A3 Canada Chris A. McGibbon1 Institute of Biomedical Engineering and Faculty of Kinesiology, University of New Brunswick, Fredericton, NB, E3B 5A3 Canada e-mail: [email protected] There is increasing interest in wearable sensor technology as a tool for rehabilitation applications in community or home environments. Recent studies have focused on evaluating inertial based sensing (accelerometers, gyroscopes, etc.) that provide only indirect measures of joint motion. Measurement of joint kinematics using flexible goniometry is more direct, and still popular in laboratory environments, but has received little attention as a potential tool for wearable systems. The aim of this study was to compare two goniometric devices: a traditional strain-gauge flexible goniometer, and a fiberoptic flexible goniometer, for measuring dynamic knee flexion/extension angles during activity of daily living: chair rise, and gait; and exercise: deep knee bends, against joint angles computed from a “gold standard” Vicon motion tracking system. Six young adults were recruited to perform the above activities in the lab while wearing a goniometer on each knee, and reflective markers for motion tracking. Kinematic data were collected simultaneously from the goniometers (one on each leg) and the motion tracking system (both legs). 1 Corresponding author. Contributed by the Bioengineering Division of ASME for publication in the JOURNAL OF BIOMECHANICAL ENGINEERING. Manuscript received December 19, 2011; final manuscript received June 1, 2012; accepted manuscript posted July 6, 2012; published online August 6, 2012. Assoc. Editor: Richard Neptune. Journal of Biomechanical Engineering Fig. 1 The two flexible goniometers used in the study. (a) Penny & Giles type flexible goniometer (Biometric’s Ltd) mounted on the right knee. (b) ShapeSensorTM fiber-optic goniometer (Measurand Inc.) mounted on the left knee. (c) Form-factor comparison of the two devices. (d) Plug-in Gait (lower extremity) marker attachment sites and joint center locations. C 2012 by ASME Copyright V AUGUST 2012, Vol. 134 / 084502-1 Downloaded From: http://biomechanical.asmedigitalcollection.asme.org/ on 01/18/2015 Terms of Use: http://asme.org/terms Fgon), when used to capture sagittal plane knee motion, relative to a “gold standard” optical tracking system (Vicon, Oxford Metrics, UK). The primary question being asked is: does the Fgon meet the measurement standards set by the traditional Egon? This information is required as a first step in evaluating the feasibility of health professionals using flexible goniometers for rehabilitation applications in a wider range of environments. 2 Methods 2.1 Participants. Six volunteers (three males and three females) participated in this study (mean 6 SD age: 23 6 2.3 years, weight: 66.9 6 11.43 kg, height: 167.8 6 11.58 cm). Participants had no musculoskeletal, neurological or sensory impairments or related disabilities. The study was approved by the institutional research ethics board, and each volunteer provided written informed consent. 2.2 Equipment and Procedures. Two goniometer devices were evaluated for measuring dynamic knee flexion/extension during activity of daily living (ADL) and exercise: (1) Egon: 2-DOF2 Penny & GilesTM; and (2) Fgon; 1-DOF ShapeSensorTM. Data from both devices were captured using a custom-built lightweight multichannel A/D acquisition device (Biological Signals Interface, or BioSITM, University of New Brunswick, Canada) carried in the participant’s hand, and tethered to a laptop computer. 2.3 Device Characteristics. Linearity of goniometer devices was determined from bench testing in the absolute range of knee motion expected during experiments (0 6 150 deg) with the flexible goniometer mounted on a large plastic reference goniometer fixed to a flat table top. Two testers performed the trials twice. Both goniometers can measure in the positive and negative angle ranges (depending on which side of the joint mounted), therefore data was collected (and averaged over five seconds trials at 200 Hz) at ten degree increments from 0 to 150 deg and 0 to 150 deg. Calibration coefficients were determined by fitting 1st order polynomials to the goniometer and reference data for three different ranges: low flexion: 0 to 670 deg (gait); moderate flexion: 0 to 6110 deg (chair rise), and; high flexion: 0 to 6150 deg (deep knee bend). 2.4 Motion Analysis Testing. To mount the goniometers, participant’s right and left legs were first fitted with Neoprene and Velcro thigh and shin segment cuffs. These nonslip cuffs were custom built with a medial pocket for mounting the goniometer end blocks, as shown in Fig. 1(b) and 1(c). The Egon was worn on the right knee and the Fgon was worn on the left knee (Fig. 1(d)) for all participants. Motion analysis data was collected with an eight camera Vicon MCam system (Oxford Metrics, UK) using the “Plug-in Gait” marker set [15] (Fig. 1(d)). BioSI and Vicon systems were triggered simultaneously and sampled at 1000 Hz and 60 Hz, respectively. Right and left knee flexion/extension angles from motion capture were processed according to Davis et al. [15]. BioSI data was downsampled to 60 Hz using a spline function in MATLAB (MathWorks Inc. Natick, MA). Participants performed the following activities: (1) Static Standing Trial. Participants were asked to stand perfectly still, arms at sides, with eyes opened and looking straight ahead and feet shoulder width apart. (2) Free Gait Trial. From a standing position at the start of the walkway, the participant walked at their preferred comfortable pace until reaching the opposite end of the walkway. (3) Sit-to-stand Trial. Participants were seated upon an armless, backless chair of adjustable height with arms folded across 2 Although both DOF were recorded from the Egon we only used the sagittal plane angles for comparison to the Fgon. the abdomen, and were instructed to rise from the chair on cue. (4) Deep Knee Bend Trial. From a standing position with feet shoulder width apart, participants were instructed to lower their center gravity by bending at the knees as much as possible to a crouch position, and then rising again to a standing position. For each of the locomotion activities, the first trial captured without marker loss (common for chair rise and deep knee bends) was selected for data analysis. 2.5 Data Analysis. Fgon angles were compared to the right knee angles estimated from the Vicon data, and Egon angles were compared to the left knee angles estimated from Vicon data. The device calibration curves were first applied to the raw goniometer data, and then the static standing offsets were removed from both the Vicon and goniometer signals. The absolute average error between the two signals was then computed. A second analysis was performed by first subtracting off the signal means, and then calculating the absolute errors (signal bias removed). Finally, correlation coefficients for the two signals were computed. In order to standardize the comparisons, for chair rise trials and deep knee bends, the signals were compared between the start of movement and erect standing. For gait trials, the signals were compared between successive heel strike or toe-off events (of the same limb), depending on the portion of knee flexion captured with Vicon. 3 Results 3.1 Goniometer Characteristics. As previously described, the Egon and Fgon were worn on the right and left knee, respectively, for all participants. Therefore only quadrant 1 of Fig. 2(a) is relevant for the Egon, and quadrant 3 of Fig. 2(a) for the Fgon. Differences between goniometers readings and known angles are also shown in Fig. 2(b). Figure 2(b) shows asymmetric linearity characteristics for both goniometers (meaning the goniometers do not have the same degree of linearity throughout positive and negative ranges), but also indicates that our choice of mounting minimized device linearity errors. 3.2 Goniometry Compared to Optical Tracking. As shown in Table 1, mean absolute errors relative to Vicon for gait and chair rise were 4.2 deg and 4.7 deg, respectively for the Egon, and 5.1 deg and 8.9 deg, respectively for the Fgon. For deep knee bends, the Fgon performed slightly better overall, having mean error of 8.5 deg compared to >11 deg for the Egon. As shown in Table 2, when signal biases were completely eliminated, errors for gait and chair rise reduced to 2.3 deg and 3.4 deg, respectively for the Egon, and 3.3 deg and 4.3 deg, respectively for the Fgon. Little improvement was observed for deep knee bends, for either Egon (10.5 deg) or Fgon (8.4 deg), when removing signal bias. Figure 3(a) shows representative results of a gait trial for Participant #1. Here, the Fgon tracked the knee better than the Egon (Egon: 4.3 deg; Fgon: 2.2 deg, Table 1), but when removing signal bias the errors decreased for the Egon to less than the Fgon (Egon: 1.9 deg; Fgon: 2.3 deg, Table 2). Figure 3(b) shows representative results of a chair rise trial for Participant #2. The Egon tracked the knee more closely than the Fgon (Egon: 3.0 deg; Fgon: 4.4 deg, Table 2), but little change was observed when removing signal bias (Egon: 2.6 deg; Fgon: 4.4 deg, Table 3). For other participants (not shown in Fig. 3), removing signal bias did reduce errors observed (Participant #4 for example—see Tables 2 and 3). Error in predicting knee angles during the deep knee bend trials was quite high for both goniometer devices. Figure 3(c) shows representative data of a deep knee bend trials for Participant #6. The Fgon was able to track knee flexion angles better than the Egon (Egon: 8.1 deg; Fgon: 3.0 deg, Table 2). This trend did not 084502-2 / Vol. 134, AUGUST 2012 Downloaded From: http://biomechanical.asmedigitalcollection.asme.org/ on 01/18/2015 Terms of Use: http://asme.org/terms Transactions of the ASME Table 2 Knee goniometer angle error relative to Vicon knee angle, after removing signal bias Egon Fig. 2 (a) Goniometer linearity test results over 0 to 150 deg and 0 to 150 deg range. Measured goniometer values are shown on the vertical axis and reference goniometer values are shown on the horizontal axis. (b) Difference between measured goniometer readings and reference goniometer. Flexion ranges used for each goniometer in the experiments are indicated. Table 1 angle Knee goniometer angle error relative to Vicon knee Egon Fgon Subject Gait Chair Bend Mean Gait Chair Bend Mean 1 2 3 4 5 6 4.29 2.62 4.19 7.04 6.60 3.34 2.13 3.04 5.78 5.97 3.15 4.83 9.76 5.26 9.93 28.33 6.91 8.08 5.39 3.64 6.63 13.78 5.55 5.42 2.23 8.31 1.99 6.82 4.59 6.71 13.55 4.39 6.96 9.73 6.40 12.24 22.22 8.53 1.78 9.74 5.84 3.04 12.67 7.08 3.58 8.76 5.61 7.33 Mean 4.68 4.15 11.38 6.74 5.11 8.88 8.53 7.50 change when signal bias was removed. Nevertheless, data in Tables 1 and 2 show each device experienced errors greater than 20 deg for both the Egon (Participant #4) and the Fgon (Participant #1). Finally, correlation coefficients were very high for all trials and subjects, ranging between 9.2–1.0. Due to the limited value of these results, we did not include them in the tables. 4 Discussion Although wearable sensor systems have great potential for applications in physical medicine and rehabilitation [8,12,16,17], Journal of Biomechanical Engineering Fgon Subject Gait Chair Bend Mean Gait Chair Bend Mean 1 2 3 4 5 6 1.94 2.59 4.63 3.22 4.17 3.52 0.62 2.61 4.26 4.68 1.21 0.79 10.94 6.15 9.06 22.03 7.32 6.60 4.50 3.78 5.99 9.98 4.23 3.64 2.29 5.00 2.02 5.95 3.22 6.95 5.47 4.38 2.09 3.86 1.79 2.05 24.22 9.47 2.60 8.44 5.04 1.56 10.66 6.28 2.24 6.08 3.35 3.52 Mean 3.35 2.36 10.35 5.35 4.24 3.27 8.56 5.35 there is no clear consensus regarding the type(s) of sensors that provide the best solutions for measuring key outcomes variables in remote environments. Inertial-based sensors show great promise in a range of applications, from identifying human activities for monitoring purposes [12,18] to detecting important gait events critical to assistive technologies for stroke and Parkinson’s disease [19,20]. Although inertial-measurement units (IMUs) can be used to measure knee flexion/extension kinematics [21–23], they are not immune to artifact. deVries et al. [24] report significant magnetic field artifacts when IMUs are used in close proximity to ferromagnetic structural supports in a motion laboratory. Iron structures are common in residential apartment buildings and care centers, and thus pose a threat to the validity of IMU instruments for remote applications. Furthermore, Kendall and Lemaire [25] report that ferromagnetic interference with mobility devices, such as walkers, wheelchairs, orthotics and prosthetic devices significantly decreases IMU measurement validity. The usability of IMU systems in remote rehabilitation environments may, therefore, be problematic. Flexible goniometers are comparatively simple to use, their data easy to analyze and interpret, and they are not susceptible to ferromagnetic influence. As with any motion capture system, however, proper mounting and alignment of sensors on the limbs, and static calibration trials, are clearly still a requirement. Our data support this fact, but also show that flexible goniometry provides a promising level of accuracy in measuring knee joint kinematics during ADL relevant to physical medicine and rehabilitation. 4.1 Flexible Goniometry as an Assessment Tool for Knee Mobility. When applying device calibration curves and a simple static calibration trial (participant standing erect with knees at full extension) to correct the joint angles, the Egon had slightly better performance during gait and chair rise activities compared to the Fgon (see Table 2). When removing all signal bias, errors were reduced for both the Egon and Fgon (see Table 3). This data suggest that for locomotor ADL, where peak knee flexion angles are typically in the 0–110 deg range (which includes chair and stair activities along with gait [13]) both goniometers can achieve good levels of accuracy, but that a more sophisticated static calibration scheme may be required to achieve better levels of accuracy for these ADLs. For deep knee bends both goniometers showed a tendency to under-predict knee flexion angles beyond 110 deg. Here the Fgon error was lower than the Egon error (see Table 2). However, the data suggest that device mounting is more critical when testing at higher flexion angles, probably due to the deformation of the body segments and mounting cuffs at higher degrees of knee flexion. This might also explain why the Fgon performed better at higher flexion angles: the neoprene cuffs were further apart for the Fgon (see Fig. 1) and; as a result, end block mounts might not have deformed as much at higher flexion angles. This suggests that mounting strategy is more relevant when being used for highflexion applications. AUGUST 2012, Vol. 134 / 084502-3 Downloaded From: http://biomechanical.asmedigitalcollection.asme.org/ on 01/18/2015 Terms of Use: http://asme.org/terms Fig. 3 Representative trials for study participants. Plots depict a close agreement for gait and chair rise, and illustrate the higher errors observed for deep knee bend trials. (a) Gait data for Participant #1. (b) Chair rise data for Participant #2. (c) Deep knee bend data for Participant #6. 4.2 Flexible Goniometery in Wearable Sensor Applications. Huddleston et al. [12] used the Penny & GilesTM goniometer with an activity monitor system [26] to document the range of knee flexion angles for different ADL. Although laboratory validation results are given as correlation coefficients, rather than absolute errors, the values (0.97–0.98) are in agreement with our study. Huddleston’s study also deployed the system remotely for long-term capture, to test whether “high-flexion” prosthetic knee components (capable of >150 deg flexion) reflect the mobility needs of normal behaving adults. They found that maximum knee angles rarely exceeded 120 deg during human activity. As discussed above, our data suggest that end block mount deformation (soft tissue and/or cuffs) at extreme flexion angles may be a significant factor in causing this under-prediction. Indramohan et al. [8] measured goniometer knee angles for chair rise, gait, stair ascent/decent, and squatting (similar to our deep 084502-4 / Vol. 134, AUGUST 2012 Downloaded From: http://biomechanical.asmedigitalcollection.asme.org/ on 01/18/2015 Terms of Use: http://asme.org/terms Transactions of the ASME knee bend), but they only validated the goniometer data for gait trials captured simultaneously with an optical tracking system (Vicon, Oxford, UK). The range of absolute error was 3–5 degrees, which is consistent with our results. Interestingly, they also report that squat knee angles were much lower (120 deg) than expected (>150 deg [27]) for this activity. As noted above, the ability of flexible goniometers to measure extreme knee flexion angles could be questioned. In terms of clinical relevance, many lower extremity pathologies can result in significant deviations of knee joint kinematics, with peak differences greater than 10 deg during walking in patients with stroke [28] and knee arthritis [29], and differences up to 20 deg for high-flexion activities (knee bends, crouching, etc.) in patients with total knee replacement [30]. The errors we report for both goniometer systems generally suggest these devices could be useful clinically, however our results emphasize that great care needs to be taken in calibrating the devices for specific applications and more research is needed on the effects of different mounting strategies. 4.3 Limitations. There were several limitations to our study. The sample size was relatively small, but similar to other studies that have evaluated goniometers. We positioned the goniometers on the medial side of the knee rather than the more traditional lateral side; this was necessary to avoid interference between the goniometer cable and knee marker. However, we have found no studies indicating that medial mounting is more prone to goniometer errors than lateral mounting, and considering our results agree with other studies, we are confident this is not a major limitation. Our data suggest the mounting cuffs may have contributed to the higher errors observed at extreme knee flexion angles. Although taping the end blocks directly to skin might have reduced this effect, this approach is less likely to be accepted in remote sensing applications than the quickly donned and doffed cuffs that we used. There are also limitations to the Plug-in Gait marker set that may have contributed to errors observed. Because this marker set was designed primarily for use in gait studies [15] errors at higher flexion activities could also be due to uncertainly in knee angle computations from marker data. However, we observed no significant abnormalities in calculated angles. Also, although crosstalk between joint axis angles due to marker misalignment is a common concern, the issue is typically more relevant to the quality of varus/valgus and axial rotation angles, which are not analyzed in this paper. Other issues not explored in this paper, but relevant to future applications outside the laboratory (clinic, community or home care settings; for example) include the influence of sensor positioning, sensitivity to off-axis motions (such as knee varus-valgus), and the potential for the cuffs to migrate during usage. Sensor positioning is generally not an issue as trained personnel are still required to help patients don and doff the devices, and the ShapeSensor device exhibits low sensitivity to off-axis rotation. The inner material of the cuffs adhered very well to skin preventing any observable cuff migration, but this would need to be monitored for long-term wear applications. 5 Conclusions Our study is the first we know of to compare a fiber-optic goniometer and a strain-gauge goniometer to a gold standard motion analysis system, for a range of knee activities relevant to rehabilitation. Correlations were very high for both goniometers against optical tracking methods for all activities studied, indicating that patterns of movement are faithfully recorded by both devices. Applications where more knee flexion range >120 deg is required may need to incorporate different mounting strategies, and a more sophisticated static calibration protocol. 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