1. Introduction
Accurate assessment of human movement is a foundational component of physical therapy practice and informs clinical decision making, identification of movement impairments, progression of rehabilitation interventions, and evaluation of patient outcomes. Functional tasks such as the sit-to-stand (STS) are frequently used to assess lower extremity strength, balance, coordination, postural control, and mobility across a wide range of clinical and non-clinical populations [
1,
2,
3,
4]. The STS task is considered biomechanically demanding because it requires coordinated trunk flexion, lower extremity force generation, dynamic postural control, and anticipatory balance adjustments during the transition from a stable seated posture to upright standing [
1,
5]. Impairments in STS performance have been associated with functional decline, increased fall risk, mobility limitations, sarcopenia, decreased gait speed and reduced independence in older adults and clinical populations [
2,
6,
7,
8,
9]. As a result, accurate assessment of STS movement quality and joint kinematics is clinically important in rehabilitation settings [
5].
Traditionally, assessment of movement quality in physical therapy has relied heavily on observational analysis and clinician interpretation. Although observational assessment remains a fundamental component of clinical practice, visual analysis may be influenced by subjectivity, variability in clinician experience, and limitations in the ability to accurately quantify complex multi-joint movement patterns [
10]. In response, motion capture technologies have increasingly been incorporated into rehabilitation, sports medicine, and educational settings to provide objective, quantifiable measures of movement performance. Historically, three-dimensional marker-based motion capture systems have been considered the gold standard for biomechanical analysis; however, these systems often require laboratory environments, reflective markers, specialized personnel, and extensive processing time, limiting their accessibility in routine clinical settings [
11,
12].
Markerless motion capture systems have emerged as a more accessible alternative capable of providing real-time movement analysis without the need for reflective markers or extensive laboratory infrastructure. These systems use camera-based tracking algorithms, depth-sensing technologies, and biomechanical modeling approaches to estimate joint kinematics and movement performance during functional activities. Markerless systems have gained increasing attention within rehabilitation and physical therapy education due to their portability, lower cost, reduced setup time, and ability to provide immediate movement feedback in clinical and educational environments [
13,
14,
15,
16]. More recently, advances in artificial intelligence and computer vision technologies have accelerated the integration of markerless motion capture into movement assessment, remote monitoring, and rehabilitation applications [
17,
18]. Previous research has demonstrated acceptable validity and reliability of several markerless motion capture systems for assessment of gait, balance, postural control, and functional movement when compared to traditional laboratory-based systems [
11,
12,
13,
16].
Despite these advancements, important questions remain regarding the comparability of measurements generated across different markerless motion capture systems. Variability in hardware configuration, camera placement, tracking algorithms, filtering methods, sampling frequency, and biomechanical modeling approaches may contribute to systematic differences in reported movement outcomes between systems, even when assessing the same task. The prior biomechanical and rehabilitation technology literature has emphasized that differences in processing pipelines and measurement methodologies can influence interpretation of movement outcomes and comparisons across systems [
19,
20]. These potential differences are clinically important because clinicians, educators, and researchers may assume that outputs generated by different systems are interchangeable or directly comparable. If substantial measurement differences exist between systems, interpretation of movement performance, longitudinal tracking of patient progress, and educational interpretation of biomechanical data may be influenced by the specific technology being used rather than true differences in movement performance.
Most studies evaluating markerless motion capture have focused on establishing criterion validity through comparison with marker-based motion capture systems, which remain the accepted reference standard for biomechanical analysis [
16,
21,
22,
23,
24]. These investigations are essential for determining the absolute accuracy of individual markerless systems. However, as markerless motion capture technologies become increasingly integrated into clinical practice, rehabilitation, and physical therapy education, clinicians and researchers are increasingly selecting between commercially available markerless platforms rather than between markerless and marker-based systems. Consequently, understanding whether different commercially available markerless systems provide comparable measurements represents a distinct and clinically relevant research question with important implications for rehabilitation, physical therapy education, and movement science.
Therefore, the purpose of this study was to evaluate differences in ROM measurements obtained from two commercially available markerless motion capture systems during STS transfers performed under varying surface conditions. It was hypothesized that systematic differences would exist between systems due to differences in hardware configuration, tracking algorithms, biomechanical modeling, and signal processing approaches. Additionally, it was hypothesized that these differences would vary across both surface and joint variables.
2. Methods
2.1. Study Design
A within-subject, repeated-measures design was used to compare ROM measurements obtained from two markerless motion capture systems during a functional sit-to-stand task. Each participant performed the task under multiple surface conditions while being simultaneously recorded by both systems, allowing for direct comparison of measurement outputs within the same movement trials. Approval to conduct this study was obtained through the University’s Institutional Review Board (IRB #26327).
2.2. Participants
A convenience sample of 50 adults (32 males, 18 females), ages 22–41 (
M = 25.6,
SD = 3.84) was recruited from a university community (See
Table 1 for all demographic information). Inclusion criteria required participants to be able to perform STS transfers independently without assistance. Exclusion criteria included current musculoskeletal injury, use of an assistive device, neurological or cognitive impairment, visual impairment, medications affecting balance or coordination, and pregnancy.
An a priori power analysis was conducted in G*Power (Version 3.1.9.6) using a repeated-measures, within-subject ANOVA framework to approximate the planned study design. The parameters entered were one group, six measures, an effect size of 0.2, a power level of 0.9, and an alpha level of 0.05. The analysis showed that 36 participants were required; however, to account for attrition and incomplete data, the researchers decided on a final sample size of 50 participants.
The final analyses were conducted using linear mixed-effects modeling to account for within-subject dependency across repeated surface, device, and joint-angle measurements. To account for this, an additional simulation-based sensitivity analysis was conducted to evaluate the adequacy of the achieved sample size under the final model structure. Simulation-based power analyses are able to accommodate both the fixed- and random-effects structure of mixed models [
25]. The simulation was conducted in RStudio (Version 2026.08.0+187) using the
simr package [
26] and retained the final structure of the reported LMM, including participant as a random intercept, and Device, Surface, Joint, and all two-way interactions as fixed effects. Device-related fixed effect coefficients were proportionally scaled while preserving the relative pattern across surfaces and joint measurements. Based on 1000 Monte Carlo simulations, the sample of 50 participants provided 89.1% power (95% CI: 87.0–91.0%) to detect a Device-related effect pattern at 80% of the magnitude observed in the fitted model, using a Type II F-test with Satterthwaite degrees of freedom. A random seed of 2026 was specified for reproducibility.
2.3. Instrumentation
Two markerless motion analysis systems, the
DARI motion capture and
Kinotek, were utilized to capture and analyze participants’ movement during STS transfers across three surfaces. The
DARI Motion capture device (DARI Motion Inc., Overland Park, KS, USA) uses a network of eight FLIR BFS-PGE-04S2C-CS cameras (Teledyne FLIR, Richmond, BC, Canada; 720 × 540-pixel resolution; 60 frames per second) and proprietary software (Captury Live version 249i, build 40aea7a74 Loud Hummingbird for ubu18) to perform full-body kinematic tracking. This device captures real-time, detailed movement data via skeletal tracking without the need for physical markers, allowing for precise measurement of joint range of motion (ROM) and overall biomechanical performance [
27]. The DARI used in this study was a fixed device and calibrated using standardized DARI calibration protocols.
The Kinotek device is a portable, markerless motion capture system that uses a single Microsoft Azure Kinect v2 depth sensing camera to capture real-time movement and estimates joint kinematics and ROM via automated tracking of anatomical landmarks [
28]. The camera has a sampling rate of 30 frames per second and combines RGB video and depth sensing technology with machine learning-based pose estimation, allowing for identification of 3D skeletal landmarks and segment orientations. Utilizing proprietary software, the estimated skeletal landmarks are used to derive the joint kinematics. Both joint-angle calculations and planes of motion are software defined and not modifiable by the user [
23]. Kinotek operates as a cloud-based platform with proprietary processing algorithms. A discrete software or algorithm version associated with the analyzed data was not available to the authors. For the current study, both systems simultaneously recorded ROM at the trunk, hips, knees, and ankles during STS transfers.
2.4. Procedure
Before data collection, participants were screened for eligibility via online screening form. Eligible participants were contacted by the researchers, who scheduled their testing session. First, participants were consented and given a basic overview of the study. Next, participants filled out basic demographic information and provided past medical history. Testing was conducted in a controlled indoor environment where the DARI system was permanently affixed. The Kinotek camera was mounted on a tripod and positioned 7 feet from the participant at hip/ASIS height and at a 6° angle. Floor markings were used to standardize the position of the camera, participant, and testing surface throughout data collection. Participants completed the sit-to-stand task across three surface conditions: a firm surface (16 in), a compliant surface (18 in, 16 in compressed), and a commode surface (16 in).
Before completing the task, a researcher demonstrated an appropriate STS transfer and instructions were verbally recited. After ensuring there were no questions, participants performed one STS transfer per surface while both motion capture systems recorded simultaneously. Rest periods were provided as needed.
2.5. Data Analysis
Descriptive and inferential analyses were conducted using JAMOVI statistical software version 2.6 [
29]. The data included ROM measurements for each joint angle, surface condition, and device. The included joint angles differed in absolute ROM magnitude and variability, so to facilitate accurate comparisons across biomechanically distinct measurements, ROM values were standardized within each joint using z-score transformations. Z-scores were calculated by subtracting the overall mean ROM for each joint from the observed ROM and dividing by the corresponding standard deviation. Raw ROM descriptive statistics for each joint angle measurement by device and surface condition are presented in
Supplementary Table S1.
A linear mixed-effects model (LMM) was conducted to examine differences in ROM measurements across devices and surfaces, while accounting for repeated observations within participants. The dependent variable was standardized ROM (zROM), and fixed effects included device (DARI vs. Kinotek), surface (firm vs. compliant vs. commode), and joint (left/right ankle dorsiflexion, left/right hip adduction, left/right hip flexion, left/right knee flexion, trunk/spine flexion), along with their interaction terms. Participant was included in the model as a random intercept to account for within-subject dependency across the repeated measurements. A priori statistical significance was set at α = 0.05.
There were three primary effects of interest: (1) the main effect of device, which examined if ROM measurements differed between the DARI and Kinotek; (2) the main effect of surface, which examined if ROM measurements differed across seating conditions; and (3) interaction effects assessing if device-related differences in ROM measurements varied as a function of surface condition and joint angle. Pairwise comparisons with appropriate multiplicity correction procedures were conducted for significant effects.
3. Results
An LMM was conducted on zROM values to assess the effects of device (DARI vs. Kinotek), surface (firm vs. compliant vs. commode), and joint while accounting for repeated observations within participants. Fixed effects for device, surface, and joint, as well as all two-way interactions, were included in the model, with participant included as a random intercept. The model converged successfully and demonstrated significantly improved fit relative to an intercept-only model, ΔR2 = 0.181, χ2(37) = 500.137, p < 0.001. The full model explained 17.9% of the variance through fixed effects alone (marginal R2 = 0.179). When including participant-level random effects (conditional R2 = 0.286), 28.6% of the variance was explained via the model. The full model also demonstrated improved fit indices relative to the nested model (AIC = 7041.659 vs. 7467.796; BIC = 7277.700 vs. 7485.499).
The analysis showed significant main effects for both
Device,
F(1, 2613) = 16.117,
p < 0.001, and
Surface F(2, 2613) = 78.976,
p < 0.001 (See
Table 2). There was no significant main effect of
Joint; however, this was expected due to the use of within-joint z-score standardization, which removed magnitude differences between joints. This finding should not be interpreted as evidence that all raw ROM values were equivalent across joints, but rather as a product of the within-joint standardization performed on the data pre-analyses. Post hoc comparisons showed that the
DARI demonstrated significantly higher zROM measurements compared to the
Kinotek (
Mdiff = 0.13,
p < 0.001). This finding represents the overall standardized device effect. Therefore, this result should not be interpreted as DARI producing greater absolute ROM for all joint-angle measurements. Turning to surface comparisons, STS transfers performed on the firm surface demonstrated significantly higher zROM measurements compared to both the commode (
Mdiff = 0.44,
p < 0.001) and compliant surface (
Mdiff = 0.43,
p < 0.001). There were no significant differences in zROM measurements between the commode and compliant surface (
p > 0.05).
There were also significant two-way interactions for
Device × Surface (
F(2, 2613) = 3.455,
p = 0.032),
Device × Joint (
F(8, 2613) = 47.339,
p < 0.001), and
surface × joint (
F(16, 2613) = 7.258,
p < 0.001; see
Table 3). Post hoc comparisons for the significant
Device × Surface interaction demonstrated that the
DARI demonstrated relatively higher zROM measurements compared to the
Kinotek under the firm surface condition (
Mdiff = 0.192,
p = 0.010). Smaller differences between the two devices were observed during the compliant and commode conditions, suggesting that device-related differences between motion capture systems may be influenced by seating stability. The significant
Device × Joint interaction suggests that system-related differences varied across biomechanical variables (see
Figure 1). Post hoc comparisons showed that the largest device-dependent differences were seen in zROM measurements for left hip adduction, right hip adduction, and trunk/spine forward lean (all
p’s < 0.05). However, there were comparatively smaller or no significant differences in zROM measurements between systems for ankle dorsiflexion or knee flexion. Finally, the significant
Surface × Joint interaction suggests that the effect of surface on zROM varied across biomechanical variables (
Figure 2). Post hoc comparisons showed that higher zROM measurements were observed for ankle dorsiflexion, hip flexion, and knee flexion during STS transfers performed on the firm surface compared to both the compliant surface and commode (all
p’s < 0.001). Hip adduction and trunk forward lean had smaller surface-related differences in zROM measurements (all
p’s > 0.05).
4. Discussion
The primary finding of this study was that the two markerless motion capture systems produced systematically different range of motion (ROM) measurements across multiple joint variables during a sit-to-stand task. These differences were consistent in direction for several movements but varied depending on the plane of motion and specific joint being analyzed. Overall, these findings demonstrate systematic differences in measurements produced by the two systems when assessing movement performance during this functional task. These findings are consistent with the prior literature demonstrating that differences in hardware configuration, biomechanical modeling, filtering techniques, and tracking algorithms may contribute to variability across motion capture technologies [
19,
20,
30,
31].
For sagittal plane movements, including ankle dorsiflexion, knee flexion, and hip flexion, the DARI produced relatively higher zROM measurements compared to the Kinotek. In contrast, the Kinotek demonstrated relatively higher zROM measurements for hip adduction and trunk forward lean. These findings suggest that the differences between the two motion capture systems may be movement-dependent, as system-related variability differed across biomechanical measures. Previous investigations comparing markerless and marker-based systems have similarly reported that measurement agreement may vary by movement plane and joint variable, particularly during complex functional tasks requiring multi-joint coordination [
11,
12,
32].
The current study was not designed to explore the underlying cause of these device-dependent differences, and any differences may reflect system-specific measurement and processing approaches. Recent reviews have emphasized that differences in pose estimation algorithms, training datasets, and biomechanical modeling techniques may contribute to variability in markerless motion capture outputs [
33]. Differences in the technical configurations of the DARI and Kinotek may provide additional context to these findings, however. The DARI utilizes a fixed eight-camera configuration, which allows movement to be captured from multiple viewing perspectives, as well as a fixed bone-length biomechanical model with distances between estimated joint centers being constrained during movement. In contrast, the Kinotek consists of a single depth-sensing camera and relies on anatomical landmark estimation from a single viewing angle. Thus, differences in both camera configuration and biomechanical modeling could contribute to differences in joint-center estimation and segment orientation between the two systems. Differences in the operational definition of specific measurements may also contribute to device-related differences. DARI defines the trunk measurement using the relationship between the pelvic and thoracic regions. In contrast, although Kinotek reports trunk forward lean as a distinct measurement from lumbar, thoracic, and overall spinal flexion, the specific anatomical landmarks used to calculate this measurement are not available to the authors. Therefore, differences in the operational definition of trunk forward lean may have contributed to the observed differences between systems. This further highlights that similarly labeled kinematic variables across markerless motion capture systems may not represent identical measurements and should therefore be interpreted cautiously when comparing measurements between systems. However, the specific source of observed differences cannot be determined, as the proprietary algorithms used by both manufacturers were not evaluated in this study.
Movement patterns were also influenced by surface condition, with relatively higher zROM values for the sagittal plane movements compared to both the compliant and commode conditions. This pattern was observed across both the DARI and Kinotek devices, suggesting that task constraints may influence movement performance during STS transfers. The prior STS literature has demonstrated that environmental and task-related factors can alter lower extremity kinematics and postural control demands during transfer performance [
1,
5,
34,
35]. However, the interaction effects showed that the magnitude of device-related differences in zROM measurements was dependent on biomechanical variables. Device-related differences were more pronounced for hip adduction and trunk forward lean under specific surface conditions. These findings highlight that device-related differences were not uniform and may depend on both the movement being assessed and the environmental context in which the movement is performed [
36,
37,
38].
The present findings should be interpreted within the context of the study design and intended objective. Previous investigations have primarily focused on establishing the criterion validity of individual markerless motion capture systems through comparison with marker-based reference standards [
16,
21,
22,
23,
24]. In contrast, the present study evaluated systematic differences in ROM measurements between two commercially available markerless motion capture systems rather than the criterion validity or absolute accuracy of either platform. Consequently, the observed differences should not be interpreted as evidence that one system provides more accurate measurements than the other. Instead, these findings suggest that measurements obtained from different commercially available markerless systems may differ systematically, even when evaluating the same functional task. This distinction has important implications for clinicians, educators, and researchers when interpreting movement data across institutions, comparing findings between studies, or monitoring performance longitudinally using different markerless technologies.
From a clinical perspective, systematic differences between markerless motion capture systems should be considered when assessing or tracking patient performance over time. Differences in ROM values may reflect variations in measurement approach rather than true changes in movement, which could influence clinical decision making if not considered. This consideration may be particularly important when motion capture technologies are used longitudinally to monitor patient progress and guide clinical decision making [
15,
31]. Therefore, consistent use of a single system may be important when monitoring progress or evaluating outcomes.
From an educational perspective, these findings could have implications for how technology-based movement data are discussed in physical therapy education. Motion capture technologies are being increasingly integrated into physical therapy curricula, and thus, awareness that different systems may produce different measurements for the same task may be relevant when teaching future PTs how to interpret biomechanical data [
14,
16].
5. Limitations
Several limitations should be considered when interpreting the findings of this study. First, the sample consisted of a relatively young and healthy population, which may not reflect movement patterns observed in older adults or clinical populations. Specifically, older adults and individuals with mobility or neurological impairments may have greater movement variability, compensatory movement strategies, and even slower movement speeds when performing STS transfers [
5,
39]. This variability may influence not only how movement is captured, but also how it is modeled by these two devices, potentially resulting in a different pattern or magnitude of systematic differences than those observed in the current sample. Thus, the present findings should not be generalized to clinical populations or older adults. Second, only a single functional task (sit-to-stand) was evaluated, and findings may not generalize to more complex or dynamic movements. Future research should evaluate these devices across other functional movements in clinical populations with greater movement variability and functional impairment.
Additionally, this study did not include a marker-based motion capture system as a reference standard. Prior work comparing squat ROM measurements between the Kinotek and Vicon marker-based system showed that correspondence in measurements between systems was dependent on the measurement, with larger differences in knee flexion and ankle dorsiflexion ROM between the systems, and similar hip flexion measurements [
23]. The DARI has also been compared to marker-based systems such as Vicon [
40] and Qualisys [
30] across different movements and kinematic variables. Similar to the Kinotek study, measurement differences and magnitude of agreement between the DARI and marker-based systems varied depending on the movements and joint angles. It is important to note that neither DARI studies did not assess a squat or similar movement to an STS. Also, to our knowledge, no study has attempted to determine which device, the DARI or Kinotek, is closer to a gold standard marker-based system. Therefore, the criterion validity and absolute measurement accuracy of either markerless system cannot be determined. However, this was consistent with the intended objective of the investigation, which was to evaluate systematic differences in ROM measurements between two commercially available markerless motion capture systems rather than establish criterion validity. Future studies incorporating both marker-based and multiple markerless systems would provide complementary information regarding both absolute measurement accuracy and inter-system comparability.
Surface conditions were not counterbalanced. All participants completed the movement in the same order (firm, compliant, then commode), which may have introduced potential order effects such as fatigue, adaptation, or task familiarization. As a result, some observed surface-related differences may reflect testing order rather than surface condition alone. Specifically, because the firm condition was always completed first, and the commode condition last, systematic changes in movement strategy may have been introduced. Indeed, some of the differences attributed to surface condition, particularly between the firm and commode conditions, could reflect the fixed testing sequence. However, the observed findings demonstrated distinct biomechanical patterns across the joint variables, rather than uniform directional changes across all measures. Surface-related effects were most pronounced for ankle dorsiflexion, knee flexion, and hip flexion variables, whereas hip adduction and trunk forward lean demonstrated comparatively smaller zROM differences across seating conditions. In addition, the strongest interaction observed in the model was the Device × Joint interaction, which suggests that system-related differences varied as a function of the biomechanical variable being assessed, rather than surface condition alone. Together, these findings suggest that the observed effects are unlikely to be attributable solely to sequencing effects. However, future studies should counterbalance testing order to better explore the influence of surface condition on ROM.
The absolute magnitude for hip adduction ROM was small across conditions, especially for the DARI and thus, measurement error may represent a greater proportion of the observed ROM. Minimum detectable angular thresholds were not specified by the manufacturers of either system; therefore, it cannot be determined whether these small frontal-plane hip excursions approached the sensitivity limits of either device. Thus, the comparatively large z-score standardized difference observed for hip adduction should be interpreted cautiously.
The use of within-joint z-score standardization allowed for comparison of biomechanically distinct joint-angle measurements to be evaluated within a single model, though this transformation does not preserve the absolute magnitude of between-device differences. Consequently, these standardized differences should not be interpreted as proportional or equivalent absolute measurement differences across the joint-angle measurements. For example, the same absolute difference in degrees may be relatively small for a joint-angle measurement with a large ROM but substantial for a measurement with a small ROM. To facilitate the interpretation of absolute magnitude of the observed device and surface differences, raw ROM values have been provided in
Supplementary Table S1. The present study did not establish
a priori thresholds for clinically acceptable between-system differences, and thus, statistical differences observed in this data should not be interpreted as evidence of clinical significance.
Additionally, differences in surface height may have contributed to observed changes in ROM. Finally, only two motion capture systems were examined, and results may not generalize to other technologies with different hardware configurations or analytical approaches.
6. Future Research
Future research should further examine measurement comparability across motion capture systems in more diverse populations and across a wider range of functional tasks. Additional work is needed to better understand the factors contributing to measurement differences, including system configuration and data processing methods. Investigating how these differences influence clinical interpretation and decision making over time may further clarify the role of motion capture technology in both practice and education.
7. Conclusions
This study evaluated differences in ROM measurements between two commercially available markerless motion capture systems during sit-to-stand performance and demonstrated systematic differences in range of motion measurements across multiple joint variables. These differences varied by movement and task condition, suggesting that systematic measurement differences may depend on the biomechanical variable and testing conditions. Surface conditions also influenced movement outcomes, and in some cases, affected the magnitude of differences observed between systems. These results highlight the importance of considering both task demands and measurement approach when interpreting movement data. From a clinical perspective, consistent use of a single motion capture system may be important when tracking performance over time, as differences between systems may reflect variation in measurement rather than true changes in movement. From an educational standpoint, these findings highlight the importance of teaching future PTs that measurement outputs may vary depending on the technology being used and that these differences should be considered when interpreting technology-derived data. Overall, this study highlights the importance of evaluating measurement differences between commercially available markerless motion capture systems as a complementary line of investigation alongside traditional criterion validation studies. Together, these approaches will enhance the interpretation and application of markerless motion capture technologies in rehabilitation, physical therapy education, and movement science.
Author Contributions
The authors confirm contribution to the paper as follows: C.V.: concept development, data collection, content expertise, and manuscript preparation. C.I.: methodology refinement, study design, statistical analyses, and manuscript preparation. M.A.: data collection, content expertise, and critical manuscript revision. All authors have read and agreed to the published version of the manuscript.
Funding
This study received no external funding.
Institutional Review Board Statement
The study was conducted in accordance with the Declaration of Helsinki, and approved by the Touro University Institutional Review Board (#26327 on 17 June 2025).
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
The datasets generated and/or analyzed during the current study are available from the corresponding author upon reasonable request.
Acknowledgments
The authors used ChatGPT (OpenAI, San Francisco, CA, USA), version GPT-5.3 Instant, to assist with language refinement and organizational support during manuscript preparation. All scientific content, data interpretation, statistical analyses, and final manuscript decisions were reviewed and approved by the authors.
Conflicts of Interest
The authors report no conflicts of interest.
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