Next Article in Journal
Highly Selective Room-Temperature Blue LED-Enhanced NO2 Gas Sensors Based on ZnO-MoS2-TiO2 Heterostructures
Previous Article in Journal
Comparison and Optimization of Generalized Stamping Machine Fault Diagnosis Models Using Various Transfer Learning Methodologies
Previous Article in Special Issue
Framework Using Multicriteria Analysis for Evaluating the Risk of Musculoskeletal Disorders
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Predicting Real-World Physical Activity in Multiple Sclerosis: An Integrated Approach Using Clinical, Sensor-Based, and Self-Reported Measures

by
Patrick G. Monaghan
1,2,
Michael VanNostrand
1,2,
Taylor N. Takla
2,3 and
Nora E. Fritz
1,2,3,4,*
1
Department of Health Care Sciences, Wayne State University, Detroit, MI 48201, USA
2
Neuroimaging and Neurorehabilitation Laboratory, Wayne State University, Detroit, MI 48201, USA
3
Translational Neuroscience Program, Wayne State University, Detroit, MI 48201, USA
4
Department of Neurology, Wayne State University, Detroit, MI 48201, USA
*
Author to whom correspondence should be addressed.
Sensors 2025, 25(6), 1780; https://doi.org/10.3390/s25061780
Submission received: 19 December 2024 / Revised: 20 February 2025 / Accepted: 11 March 2025 / Published: 13 March 2025
(This article belongs to the Special Issue Advanced Sensors in Biomechanics and Rehabilitation Applications)

Abstract

:
Multiple sclerosis (MS) is a chronic neurodegenerative disease characterized by mobility impairments that limit physical activity and reduce quality of life. While traditional clinical measures and participant-reported outcomes provide valuable insights, they often fall short of fully capturing the complexities of real-world mobility. This study evaluates the predictive value of combining sensor-derived clinical measures and participant-reported outcomes to better forecast prospective physical activity levels in individuals with MS. Forty-six participants with MS completed surveys assessing fatigue, concern about falling, and perceived walking ability (MSWS-12), alongside sensor-based assessments of gait and balance. Over three months, participants wore Fitbit devices to monitor physical activity, including step counts and total activity levels. Forward stepwise regression revealed that a combined model of participant-reported outcomes and sensor-derived measures explained the most variance in future physical activity, with MSWS-12 and backward walking velocity emerging as key predictors. These findings highlight the importance of integrating subjective and objective measures to provide a more comprehensive understanding of physical activity patterns in MS. This approach supports the development of personalized interventions aimed at improving mobility, increasing physical activity, and enhancing overall quality of life for individuals with MS.

1. Introduction

Multiple Sclerosis (MS) is a chronic, neurodegenerative disorder characterized by the demyelination of axons throughout the central nervous system [1]. Due to the underlying pathology of MS, individuals with MS often report significant walking and balance impairments [2,3,4], impacting 70% of the MS community [2]. These impairments can reduce their ability to engage in physical activity, a key factor in maintaining overall quality of life [5,6]. In fact, individuals with MS have lower physical activity levels than the general population, averaging almost 4000 fewer steps per day [7,8,9]. Engaging in physical activity is crucial for individuals with MS, as it provides numerous health benefits, such as reducing fatigue [7], improving walking ability [8], and enhancing overall quality of life [6]. Increasing physical activity may also slow the progression of MS [9]. Therefore, understanding the challenges posed by MS-related mobility impairments is essential for developing effective strategies to promote and sustain physical activity across the MS community.
Traditional clinical assessments have long been the primary tools for predicting physical activity levels in individuals with MS. These methods typically include collecting subjective patient history, evaluating clinical characteristics, and conducting assessments of walking and balance. For example, a lower score on the Expanded Disability Status Scale (EDSS), a clinical scale of disease progression in MS, has been identified as a significant predictor of physical activity in this population [10]. Further clinical assessments of functional mobility, such as balance and walking speed, have also been associated with physical activity [11,12,13]. In addition to these clinical assessments, participant-reported outcomes like fear of falling [14], fatigue [14], and perceived walking capacity [15] have also been shown to impact activity levels. While these traditional assessments provide valuable insights, they often fall short in capturing the full spectrum of real-world physical activity levels experienced by the MS community. Furthermore, self-reported measures, such as the Godin Leisure–Time Exercise Questionnaire [16], are commonly used to assess physical activity in individuals with MS due to their ease of administration; however, they are limited by potential recall bias, and may not accurately reflect real-world activity levels [17]. The limitations of these conventional approaches highlight the need for more accurate and comprehensive predictors of physical activity. Identifying such predictors is crucial for informing targeted interventions that can effectively address the unique mobility challenges faced by individuals with MS, ultimately leading to more personalized and effective treatment strategies.
In recent years, wearable and sensor-based technologies have emerged as valuable tools for assessing functional mobility in individuals with MS [18]. Body-worn inertial measurement units provide portable, validated, reliable, and objective measures of balance and gait that are sensitive to changes in MS [19,20]. For example, sensor-based versions of traditional mobility assessments, such as the instrumented Timed Up and Go (iTUG), sit-to-stand, and gait and balance assessments, offer quantitative insights into motor function [21]. Research has also demonstrated that sensor-derived outcomes, such as backward walking (BW) velocity, can predict prospective physical activity levels in individuals with MS [22]. The addition of clinical sensors to assess gait and balance can greatly improve the prediction of physical activity levels in individuals with MS. Wearable sensors offer more sensitive and objective measures of mobility impairments that might be missed by traditional clinical assessments [23,24]. For instance, recent studies have shown that sensor-based gait and balance evaluations can identify subtle deficits that standard tests, like the Timed 25-Foot Walk, may overlook [23]. Additionally, sensor-derived mobility assessments can address the limitations of self-reported measures, which often fail to capture important details and may compromise sensitivity and accuracy. By combining sensor-based mobility data with patient-reported disability scores, we can enhance the ability to predict physical activity levels in individuals with MS. Therefore, wireless inertial sensor-derived clinical measures not only provide clinically valuable insights into gait and motor function, but also hold promise as a useful tool for predicting future physical activity levels in individuals with MS.
The complex nature of mobility impairments in MS necessitates a multifaceted approach to predicting real-world physical activity. While traditional clinical assessments and self-reported measures provide valuable insights into mobility and physical activity in MS, they have notable limitations. Many existing prediction models rely on subjective reports, which are prone to recall bias and may not accurately reflect real-world activity levels. Similarly, commonly used clinical scales such as the Patient-Determined Disease Steps (PDDS) scale and (EDSS) primarily assess overall disability and walking function in structured settings, but do not fully capture the complexity of daily activity patterns. Rather than replacing these established measures, we propose integrating participant-reported outcomes with objective, sensor-derived clinical mobility measures that may enhance their predictive ability. We propose that the integration of participant-reported outcomes and sensor-derived clinical measures of mobility could significantly enhance our ability to predict prospective physical activity levels in individuals with MS. By adopting this holistic approach, we aim to capture a more comprehensive and nuanced understanding of mobility challenges and physical activity patterns in MS. Notably, more accurate predictions of physical activity could pave the way for highly personalized interventions, tailored to the specific needs of individuals with MS. Such targeted strategies have the potential to more effectively maintain or improve physical activity levels, ultimately leading to better health outcomes and quality of life for the MS community.
Therefore, the aim of this study is to comprehensively assess the predictive value of participant-reported outcomes and sensor-derived clinical measures for prospective physical activity in individuals with MS. By examining these measures both independently and in combination, we seek to develop a more accurate and nuanced approach to predicting real-world physical activity levels. The findings from this study could transform approaches to maintaining and improving physical activity in people with MS, ultimately leading to improved outcomes such as preserving mobility, promoting independence, and enhancing overall health and quality of life.

2. Materials and Methods

2.1. Participants

All study procedures were approved by the Wayne State Institutional Review Board, and all participants provided informed consent in accordance with the Declaration of Helsinki. The eligibility criteria included being 18 years or older, having a diagnosis of MS based on the McDonald criteria [25], and having a Patient-Determined Disease Steps (PDDS) score ≤ 6, indicating the ability to ambulate with or without an assistive device ≥ 50% of the time [26]. Participants were excluded if they experienced an MS relapse or exacerbation within the past 30 days, used corticosteroids in the past 30 days, had a comorbid neurologic disorder, a condition affecting cognitive or motor function, or were unable to follow study commands.

2.2. Participant-Reported Outcomes

Participants completed surveys to provide demographic information and assess disease severity using the PDDS scale. Concern about falling (CAF) was assessed via the Fall Efficacy Scale-International (FES-I), a validated and reliable tool for assessing concern about individuals with MS falling [27,28]. Fatigue impact was assessed using the Modified Fatigue Impact Scale (MFIS), a 21-item self-reported measure [29]. Higher scores on the MFIS indicate a greater impact of fatigue on daily activities. Perceived walking capacity was assessed through the 12-Item Multiple Sclerosis Walking Scale (MSWS-12), a 12-item questionnaire in which participants rate their MS-related mobility limitations over the past 2 weeks using a 5-point scale, ranging from 1 (not at all) to 5 (extremely) [30].

2.3. Sensor-Derived Clinical Measures

Participants completed the Timed 25-Foot Walk in both the forward walking (FW) and BW directions. Participants completed two trials in each direction at a self-selected, comfortable walking speed. The FW and BW velocities were then computed and used in the analysis. The T25FW, widely used to assess ambulation disability in individuals with MS, is reliable, valid, and clinically meaningful in MS [22,31].
Participants wore six wireless Opal inertial sensors (128 Hz; APDM Inc., Portland, OR, USA) to measure balance using Mobility Lab’s ISway protocol [32]. They completed two 30 s trials of static balance with eyes closed feet together (ECFT). During this test, participants stood still with arms crossed comfortably on their chests and their eyes closed and feet were placed as close together as possible. This balance task was selected for its complexity, as it manipulates both the base of support and visual input—key factors in balance control [33]. Sway measures were averaged across the two trials. The total sway area was used in the analysis [19].
The instrumented push-and-release test assessed reactive balance [34]. Participants stood with feet shoulder-width apart as research staff placed hands on their scapulae and instructed them to lean backward until their body’s midline slightly exceeded their heels in the sagittal plane. After holding this position for 2–5 s, the examiner abruptly removed their hands, prompting participants to regain balance. Reactive balance was quantified using sensor-derived metrics from Opal inertial sensors [35]. Metrics included time to stabilize, defined as the interval between release and the trunk becoming stationary (lumbar sensor acceleration < 7% of gravity and rotational rate < 7°). Outcomes were averaged across three test trials following two familiarization trials. The data were processed using validated MATLAB (version 2023b) algorithms [35,36], previously applied in individuals with MS and other populations, including those with concussion and traumatic brain injury [37,38,39].

2.4. Prospective Physical Activity

Participants were provided with a Fitbit Versa 2 smartwatch to passively record physical activity data over a 3-month period using the Fitabase software platform. The Fitbit Versa 2 utilizes a triaxial accelerometer and optical heart rate sensors to estimate movement patterns, including activity intensities (e.g., active minutes at various levels) and metabolic equivalent minutes. These estimates are derived from a combination of basal metabolic rate (adjusted for age, sex, height, and weight), accelerometry data, and heart rate measurements. From the Fitabase (Fitabase, San Diego, CA, USA) platform, we extracted metrics such as sedentary minutes, lightly active minutes, fairly active minutes, very active minutes, and total steps [40,41]. Participants were instructed to wear the Fitbit device as consistently as possible throughout the monitoring period. For physical activity measures, we included both prospective daily step counts and daily total activity levels, as a previous study highlighted their distinction as separate constructs of physical activity and underscored the importance of measuring and reporting domain-specific activity [39]. To ensure valid wear time, adherence was defined as wearing the device for at least 70% of the 3-month period, with a valid day requiring a minimum of 10 h of wear time [42,43,44]. Fitbits have demonstrated reliability and validity in measuring physical activity levels in individuals with MS [45,46]. Studies have shown strong agreement between wrist-worn Fitbit devices and waist-worn ActiGraph devices [47]. Further, the wrist-worn device was selected for its feasibility, comfort, and lower invasiveness during the three-month monitoring period to help ensure compliance.

2.5. Statistical Analyses

All variables are reported as mean ± standard deviation unless otherwise specified. Data normality was assessed by examining skewness and kurtosis values. To evaluate relationships between prospective physical activity, participant-reported outcomes, and sensor-derived measures, Pearson’s correlation coefficients (r) or Spearman’s rank correlation coefficients (ρ) were calculated, depending on data distribution. Forward stepwise multiple linear regression models were employed to identify significant predictors. Model 1 included patient-reported outcomes, model 2 included sensor-derived measures, and model 3 incorporated both sets of variables (see Figure 1). Model selection was guided by the Akaike Information Criterion (AIC), which accounts for the number of predictors in each model [48]. A lower AIC value indicates a better model fit, allowing for the direct comparison of models with varying numbers of variables. To assess the contribution of individual predictors and the variance explained by each model, standardized beta coefficients (β) and R2 values were reported. All regression models were adjusted for age and PDDS. Statistical analyses were performed using SPSS version 29.0 (SPSS Inc., Chicago, IL, USA).

3. Results

A convenience sample of 56 individuals with MS was included in the study. A total of 11 individuals did not meet the valid wear time criteria outlined in the methods, so the analyses were conducted in 45 individuals with MS. Table 1 summarizes the demographic and clinical characteristics of the sample. Participants had an average age of 51.16 ± 11.12 years, reported low levels of disability on the PDDS scale (median = 1), and were predominantly female (84%). During the three-month monitoring period, device wear-time compliance was high, with participants wearing the device for an average of 1299 ± 109 min per day (maximum minutes per day = 1440). Participants took an average of 5947 ± 3079 steps per day, reflecting low levels of physical activity that do not meet step count recommendations of 7500 daily steps [49,50].

3.1. 3-Month Total Step Count

Regarding 3-month steps per day, significant negative correlations were observed with PDDS (ρ = −0.40, p < 0.01), MSWS-12 (ρ = −0.50, p < 0.01), and FES-I (ρ = −0.44, p < 0.01). These results indicate that higher step counts are associated with lower disease severity (PDDS), better self-reported walking abilities (MSWS-12), and lower concern about falling (FES-I). Significant positive correlations were observed for walking velocity in both the forward (r = 0.45, p < 0.01) and backward (r = 0.57, p < 0.01) directions, indicating that higher walking speeds are associated with increased step counts (Table 2).
The results of the forward stepwise linear regressions examining 3-month average daily steps are presented in Table 3 and Figure 1. Model 1 (participant-reported outcomes) was significant (F(3,41) = 5.29, p < 0.01), and MSWS-12 (β = −0.68, T = −2.65, p < 0.01) was the only significant predictor remaining after correcting for age and PDDS, with the final model explaining 28% of the variance in the prospective 3-month steps per day (R2 = 0.28). Model 2 (sensor-derived measures) was also significant (F(3,41) = 7.20, p < 0.01), and BW velocity was the only significant predictor for the prospective 3-month daily steps (β = 0.57, T = 3.44, p < 0.01; R2 = 0.36). Model 3, including both participant-reported and sensor-derived measures, was significant (F(4,40) = 7.35, p < 0.01), with both MSWS-12 and BW velocity significantly contributing to the model. Specifically, for 3-month steps per day, the inclusion of both variable types explained more variance, as indicated by R2 = 0.42.

3.2. 3-Month Total Activity

Regarding 3-month total physical activity, significant negative correlations were observed with PDDS (ρ = −0.49, p < 0.01), MSWS-12 (ρ = −0.59, p < 0.01), and FES-I (ρ = −0.51, p < 0.01). Positive correlations were also seen with forward walking velocity (r = 0.50, p < 0.01) and backward walking velocity (r = 0.54, p < 0.01) (Table 2).
The results of the forward stepwise linear regressions examining 3-month total physical activity are presented in Table 4 and Figure 2. Model 1 (participant-reported outcomes) was significant (F(3,41) = 7.98, p < 0.01), and MSWS-12 (β = −0.74, T = −3.08, p < 0.01) was the only participant-reported outcome contributing to the model, accounting for 38% of the variance in 3-month total activity (R2 = 0.38). Model 2 (sensor-derived measures) was also significant (F(3,41) = 6.39, p < 0.01), and BW velocity was the only significant predictor of 3-month daily total activity (β = 0.41, T = 2.40, p = 0.02; R2 = 0.32). Model 3, which included both participant-reported and sensor-derived measures, was also significant (F(4,40) = 7.54, p < 0.01), and MSWS-12 and BW velocity significantly contributed to the model. Specifically, for the 3-month daily total activity, the inclusion of both variable types explained more variance, as indicated by R2 = 0.43 for both outcomes.

4. Discussion

This study aimed to comprehensively assess the predictive value of participant-reported outcomes and sensor-derived clinical measures for prospective physical activity in individuals with MS. We found that a combined model, incorporating both participant-reported outcomes and sensor-derived clinical measures, explained the greatest variance in prospective physical activity, including total activity levels and step counts. Notably, significant predictors in the final model included the MSWS-12, a measure of perceived walking ability, and BW velocity, an objective sensor-derived functional assessment. These findings underscore the importance of integrating subjective and objective measures to more effectively predict future physical activity. This is impactful, as many individuals with MS do not meet physical activity guidelines, despite their benefits, including reduced fatigue, improved mobility, and enhanced quality of life. Identifying sensitive predictors supports tailored interventions to enhance independence and well-being, enabling proactive strategies to preserve mobility and quality of life.
Our findings underscore the importance of a comprehensive, multifaceted approach to predicting physical activity in individuals with MS. By demonstrating the complementary value of sensor-derived clinical measures and participant-reported outcomes, our study builds on and extends previous research, which has often focused on these domains in isolation. For instance, a cluster of participant-reported outcomes such as perceived walking capacity, pain and depression, and fatigue were associated with physical activity [51,52]. Prior work has also shown that the frequency and severity of participant-reported MS symptoms [53] and fear of falling [54] also influence physical activity levels in MS, emphasizing the critical role of subjective experiences in understanding engagement levels. Similarly, clinical mobility measures have also been shown to be associated with physical activity [13,22], showing that objective assessments like walking speed and balance are strongly associated with activity levels. Our findings uniquely contribute to this body of work by integrating these two perspectives, demonstrating that their combined predictive value exceeds what either can achieve alone. Sensor-derived measures offer the precise, objective quantification of mobility function, such as backward walking velocity, which is particularly sensitive to subtle impairments and predicting prospective activity. In contrast, participant-reported outcomes capture subjective factors—like confidence in walking ability and perceived limitations—that directly influence an individual’s willingness and ability to engage in physical activity. This integrated approach reflects the growing consensus in MS research that mobility impairments are inherently multidimensional and cannot be fully understood through single-metric assessments [39]. By aligning objective and subjective measures, our study provides a more nuanced framework for predicting physical activity, supporting the development of targeted, participant-centered interventions. These results further underscore the need for the continued exploration of hybrid models to address the complex interplay of factors influencing physical activity in MS.
Previous studies have shown that older adults and individuals with MS or Parkinson’s disease often experience a significant mismatch between their perceived physical limitations and actual functional capacity, which can profoundly impact their engagement in physical activity [55,56]. For example, Gunn et al. reported that 50% of individuals with MS displayed a notable disparity between their perceived and physiological fall risk, highlighting the need to consider both dimensions when evaluating fall risk in this population [55]. This discordance may be particularly pronounced in neurological conditions, where factors such as cognitive impairments, fatigue, and psychological barriers can heavily influence willingness to engage in physical activity, regardless of physiological ability. By integrating objective sensor-derived measurements with participant-reported outcomes, our study provides a holistic framework that captures both the physiological and psychological aspects of mobility. This comprehensive approach not only improves the accuracy of physical activity predictions, but also sheds light on the intricate relationship between perceived and actual functions.
Interestingly, the only significant predictor from the participant-reported outcomes model was the MSWS-12, a measure of perceived walking capacity. Increases in perceived walking capacity were associated with more total activity and more steps. This outcome corroborates previous work that has also found significant associations between MSWS-12 and physical activity in MS [15,57]. This supports prior work that has established an individual’s perception of their capacity as well as the MS-related impairment and disability as being dimensions of physical activity barriers in MS [58], highlighting the utility of such outcomes in predicting those at risk of physical inactivity. It is important to consider that other assessments included within this model, such as the MFIS, were not significant predictors.
While self-reported fatigue is frequently considered a barrier to engaging in physical activity for individuals with MS [14,59], findings on this relationship are inconsistent. Some studies have found a link between higher fatigue and lower physical activity [60,61], while others report minimal or no association [62,63,64]. Inconsistencies between self-reported fatigue and physical activity levels in MS may arise from several factors. Inconsistencies in the definitions of fatigue and the wide range of fatigue scales used across studies can lead to differing results [65,66]. Notably, our cohort had a relatively low average MFIS score (mean = 33, SD = 18), while previous studies have used a cutoff of 38 to distinguish fatigued from non-fatigued individuals [29,67]. This suggests that our sample may not fully represent the broader MS population, highlighting the need for future studies to include a wider range of fatigue levels in individuals with MS. Additionally, participant characteristics, including age, disability levels, psychological factors such as anxiety and depression, and differences in MS subtypes, may influence the relationship between fatigue and physical activity.
While previous studies have found a significant correlation between higher FES-I scores and lower physical activity levels in people with MS [54], FES-I was not a significant predictor in our model. This discrepancy may be context-dependent, influenced by differences in how physical activity is measured. Prior studies often relied on self-reported activity, which may lack accuracy or sensitivity and differ in its correlation with objective measures [68]. In contrast, our study used accelerometers to capture activity, including total steps and the sum of light, moderate, and vigorous activity minutes. These objective measures may better reflect actual activity levels, but could explain the lack of association with FES-I in our findings. Moreover, a one-time assessment of CAF using the FES-I may not fully capture fluctuations in concern of falling over time. Future studies should consider ongoing assessments of CAF alongside week-to-week physical activity tracking to better understand their dynamic relationship.
BW velocity emerged as the only significant sensor-derived clinical predictor of prospective steps and activity minutes, outperforming traditional assessments such as forward walking and standing balance. This finding highlights the potential utility of BW as a clinical assessment with predictive validity for future activity levels. Consistent with prior research showing that better BW performance correlates with higher prospective vigorous activity in individuals with MS [22], this outcome underscores the unique demands of backward walking. It challenges the postural control system [69], engages multi-domain cognitive functioning [70,71], relies heavily on proprioceptive sensory input [72,73], and effectively differentiates MS fallers from non-fallers [74]. These characteristics may make BW a more sensitive predictor of prospective physical activity, reflecting the dynamic and complex environments where activity occurs.
This study has several limitations that should be considered. First, the majority of participants had relapsing–remitting MS (Table 1), the most common subtype of the disease [75]. While this enhances the relevance of our findings to this population, it may limit generalizability to individuals with other MS subtypes, such as secondary progressive or primary progressive MS. Second, despite participants being instructed to wear the Fitbit device as much as possible, there was variability in adherence to wear time, which may have influenced physical activity outcomes. However, as shown in Table 1, the overall adherence and wear time rate were reasonably compliant across all participants. Third, although our final models did not include psychological factors such as anxiety and depression [76], these variables may also influence the relationship between clinical measures and physical activity. For example, anxiety and depression are common in MS, with prevalence rates significantly higher than in the general population. Depression affects 27–54% of MS patients, while anxiety disorders impact up to 45% [76,77]. These conditions reduce quality of life, correlate with greater disability and fatigue, and discourage physical activity [78,79], meaning that individuals with MS experiencing higher depression and anxiety are less likely to adhere to the exercise regimens essential for managing their condition [78]. Therefore, future work should incorporate these factors to provide a more comprehensive understanding of the determinants of physical activity in MS.

5. Conclusions

This study highlights the novel integration of participant-reported outcomes and sensor-derived clinical measures to predict prospective physical activity in individuals with MS. Our findings reveal that combining these domains provides superior predictive power compared to using either in isolation, addressing a critical gap in the understanding of factors influencing real-world activity levels. Specifically, BW velocity and perceived walking capacity emerged as significant predictors, emphasizing the importance of both objective functional performance and subjective perceptions of mobility. By demonstrating the complementary strengths of these measures, our work advances the field toward more comprehensive and accurate prediction models. This approach has the potential to inform targeted, individualized interventions aimed at preserving mobility and promoting engagement in physical activity, thereby improving health outcomes and quality of life for individuals with MS.

Author Contributions

Conceptualization, P.G.M., T.N.T. and M.V.; methodology, P.G.M., T.N.T. and M.V.; data curation, P.G.M., T.N.T. and M.V.; formal analysis, M.V.; visualization, M.V. and P.G.M.; writing—original draft preparation, P.G.M.; review and editing, P.G.M., T.N.T., M.V. and N.E.F.; supervision, N.E.F.; funding acquisition, N.E.F.; approval of final version of the manuscript, P.G.M., M.V., T.N.T. and N.E.F. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the National Multiple Sclerosis Society Research Grant (RG-2111-38718), the National Multiple Sclerosis Society Mentor-Based Postdoctoral Fellowship in Rehabilitation Research (MB-2107-38295), and the NIH (R21HD106133, F31HD116491).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board of Wayne State University (092819B3E on 1 October 2019).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are available upon request from the corresponding author.

Acknowledgments

The authors would like to thank those who participated in this study and all those who helped distribute and spread awareness of our study.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Trapp, B.D.; Nave, K.A. Multiple Sclerosis: An Immune or Neurodegenerative Disorder? Annu. Rev. Neurosci. 2008, 31, 247–269. [Google Scholar] [CrossRef] [PubMed]
  2. LaRocca, N.G. Impact of Walking Impairment in Multiple Sclerosis: Perspectives of Patients and Care Partners. Patient 2011, 4, 189–201. [Google Scholar] [CrossRef]
  3. Comber, L.; Galvin, R.; Coote, S. Gait Deficits in People with Multiple Sclerosis: A Systematic Review and Meta-Analysis. Gait Posture 2017, 51, 25–35. [Google Scholar] [CrossRef]
  4. Comber, L.; Sosnoff, J.J.; Galvin, R.; Coote, S. Postural Control Deficits in People with Multiple Sclerosis: A Systematic Review and Meta-Analysis. Gait Posture 2018, 61, 445–452. [Google Scholar] [CrossRef] [PubMed]
  5. Motl, R.W. Benefits, Safety, and Prescription of Exercise in Persons with Multiple Sclerosis. Expert. Rev. Neurother. 2014, 14, 1429–1436. [Google Scholar] [CrossRef] [PubMed]
  6. Motl, R.W.; Gosney, J.L. Effect of Exercise Training on Quality of Life in Multiple Sclerosis: A Meta-Analysis. Mult. Scler. J. 2008, 14, 129–135. [Google Scholar] [CrossRef]
  7. Pilutti, L.A.; Greenlee, T.A.; Motl, R.W.; Nickrent, M.S.; Petruzzello, S.J. Effects of Exercise Training on Fatigue in Multiple Sclerosis: A Meta-Analysis. Psychosom. Med. 2013, 75, 575–580. [Google Scholar] [CrossRef]
  8. Pearson, M.; Dieberg, G.; Smart, N. Exercise as a Therapy for Improvement of Walking Ability in Adults With Multiple Sclerosis: A Meta-Analysis. Arch. Phys. Med. Rehabil. 2015, 96, 1339–1348.e7. [Google Scholar] [CrossRef]
  9. Dalgas, U.; Stenager, E. Exercise and Disease Progression in Multiple Sclerosis: Can Exercise Slow down the Progression of Multiple Sclerosis? Ther. Adv. Neurol. Disord. 2012, 5, 81–95. [Google Scholar] [CrossRef]
  10. Beckerman, H.; De Groot, V.; Scholten, M.A.; Kempen, J.C.E.; Lankhorst, G.J. Physical Activity Behavior of People with Multiple Sclerosis: Understanding How They Can Become More Physically Active. Phys. Ther. 2010, 90, 1001–1013. [Google Scholar] [CrossRef]
  11. Ketelhut, N.B.; Kindred, J.H.; Pimentel, R.E.; Hess, A.M.; Tracy, B.L.; Reiser, R.F.; Rudroff, T. Functional Factors That Are Important Correlates to Physical Activity in People with Multiple Sclerosis: A Pilot Study. Disabil. Rehabil. 2018, 40, 2416–2423. [Google Scholar] [CrossRef]
  12. Kehoe, M.; Saunders, J.; Jakeman, P.; Coote, S. Predictors of the Physical Impact of Multiple Sclerosis Following Community-Based, Exercise Trial. Mult. Scler. J. 2015, 21, 590–598. [Google Scholar] [CrossRef] [PubMed]
  13. Kahraman, T.; Savci, S.; Coskuner-Poyraz, E.; Ozakbas, S.; Idiman, E. Determinants of Physical Activity in Minimally Impaired People with Multiple Sclerosis. Clin. Neurol. Neurosurg. 2015, 138, 20–24. [Google Scholar] [CrossRef] [PubMed]
  14. Rzepka, M.; Toś, M.; Boroń, M.; Gibas, K.; Krzystanek, E. Relationship between Fatigue and Physical Activity in a Polish Cohort of Multiple Sclerosis Patients. Medicina 2020, 56, 726. [Google Scholar] [CrossRef] [PubMed]
  15. Kohn, C.G.; Coleman, C.I.; Michael White, C.; Sidovar, M.F.; Sobieraj, D.M. Mobility, Walking and Physical Activity in Persons with Multiple Sclerosis. Curr. Med. Res. Opin. 2014, 30, 1857–1862. [Google Scholar] [CrossRef]
  16. Sikes, E.M.; Richardson, E.V.; Cederberg, K.J.; Sasaki, J.E.; Sandroff, B.M.; Motl, R.W. Use of the Godin Leisure-Time Exercise Questionnaire in Multiple Sclerosis Research: A Comprehensive Narrative Review. Disabil. Rehabil. 2019, 41, 1243–1267. [Google Scholar] [CrossRef]
  17. Gosney, J.L.; Scott, J.A.; Snook, E.M.; Motl, R.W. Physical Activity and Multiple Sclerosis: Validity of Self-Report and Objective Measures. Fam. Community Health 2007, 30, 144–150. [Google Scholar] [CrossRef]
  18. Woelfle, T.; Bourguignon, L.; Lorscheider, J.; Kappos, L.; Naegelin, Y.; Jutzeler, C.R. Wearable Sensor Technologies to Assess Motor Functions in People with Multiple Sclerosis: Systematic Scoping Review and Perspective. J. Med. Internet Res. 2023, 25, e44428. [Google Scholar] [CrossRef]
  19. Monaghan, P.G.; Monaghan, A.S.; Hooyman, A.; Fling, B.W.; Huisinga, J.M.; Peterson, D.S. Utilizing the ISway to Identify and Compare Balance Domain Deficits in People with Multiple Sclerosis. Mult. Scler. Relat. Disord. 2023, 73, 104645. [Google Scholar] [CrossRef]
  20. Mancini, M.; King, L.; Salarian, A.; Holmstrom, L.; McNames, J.; Horak, F.B. Mobility Lab to Assess Balance and Gait with Synchronized Body-Worn Sensors. J. Bioeng. Biomed. Sci. 2011, 7. [Google Scholar] [CrossRef]
  21. Salarian, A.; Horak, F.B.; Zampieri, C.; Carlson-Kuhta, P.; Nutt, J.G.; Aminian, K. ITUG, a Sensitive and Reliable Measure of Mobility. IEEE Trans. Neural Syst. Rehabil. Eng. 2010, 18, 303–310. [Google Scholar] [CrossRef]
  22. Monaghan, P.G.; Takla, T.N.; Chargo, A.N.; Edwards, E.M.; Yu, B.; Myers, E.; Daugherty, A.M.; Fritz, N.E. Measurement Properties of Backward Walking and Its Sensitivity and Feasibility in Predicting Falls in People With Multiple Sclerosis. Int. J. MS Care 2024, 26, 155–166. [Google Scholar] [CrossRef] [PubMed]
  23. Spain, R.I.; St. George, R.J.; Salarian, A.; Mancini, M.; Wagner, J.M.; Horak, F.B.; Bourdette, D. Body-Worn Motion Sensors Detect Balance and Gait Deficits in People with Multiple Sclerosis Who Have Normal Walking Speed. Gait Posture 2012, 35, 573–578. [Google Scholar] [CrossRef]
  24. Angelini, L.; Hodgkinson, W.; Smith, C.; Dodd, J.M.; Sharrack, B.; Mazzà, C.; Paling, D. Wearable Sensors Can Reliably Quantify Gait Alterations Associated with Disability in People with Progressive Multiple Sclerosis in a Clinical Setting. J. Neurol. 2020, 267, 2897–2909. [Google Scholar] [CrossRef] [PubMed]
  25. Polman, C.H.; Reingold, S.C.; Banwell, B.; Clanet, M.; Cohen, J.A.; Filippi, M.; Fujihara, K.; Havrdova, E.; Hutchinson, M.; Kappos, L.; et al. Diagnostic Criteria for Multiple Sclerosis: 2010 Revisions to the McDonald Criteria. Ann. Neurol. 2011, 69, 292–302. [Google Scholar] [CrossRef] [PubMed]
  26. Hohol, M.J.; Orav, E.J.; Weiner, H.L. Disease Steps in Multiple Sclerosis: A Longitudinal Study Comparing Disease Steps and EDSS to Evaluate Disease Progression. Mult. Scler. J. 1999, 5, 349–354. [Google Scholar] [CrossRef]
  27. Scholz, M.; Haase, R.; Trentzsch, K.; Weidemann, M.L.; Ziemssen, T. Fear of Falling and Falls in People with Multiple Sclerosis: A Literature Review. Mult. Scler. Relat. Disord. 2021, 47, 102609. [Google Scholar] [CrossRef]
  28. Van Vliet, R.; Hoang, P.; Lord, S.; Gandevia, S.; Delbaere, K. Falls Efficacy Scale-International: A Cross-Sectional Validation in People with Multiple Sclerosis. Arch. Phys. Med. Rehabil. 2013, 94, 883–889. [Google Scholar] [CrossRef]
  29. Kos, D.; Kerckhofs, E.; Carrea, I.; Verza, R.; Ramos, M.; Jansa, J. Evaluation of the Modified Fatigue Impact Scale in Four Different European Countries. Mult. Scler. J. 2005, 11, 76–80. [Google Scholar] [CrossRef]
  30. Hobart, J.C.; Riazi, A.; Lamping, D.L.; Fitzpatrick, R.; Thompson, A.J. Measuring the Impact of MS on Walking Ability: The 12-Item MS Walking Scale (MSWS-12). Neurology 2003, 60, 31–36. [Google Scholar] [CrossRef]
  31. Motl, R.W.; Cohen, J.A.; Benedict, R.; Phillips, G.; LaRocca, N.; Hudson, L.D.; Rudick, R. Validity of the Timed 25-Foot Walk as an Ambulatory Performance Outcome Measure for Multiple Sclerosis. Mult. Scler. 2017, 23, 704–710. [Google Scholar] [CrossRef] [PubMed]
  32. Mancini, M.; Salarian, A.; Carlson-Kuhta, P.; Zampieri, C.; King, L.; Chiari, L.; Horak, F.B. ISway: A Sensitive, Valid and Reliable Measure of Postural Control. J. Neuroeng. Rehabil. 2012, 9, 59. [Google Scholar] [CrossRef] [PubMed]
  33. Horak, F.B.; Wrisley, D.M.; Frank, J. The Balance Evaluation Systems Test (BESTest) to Differentiate Balance Deficits. Phys. Ther. 2009, 89, 484–498. [Google Scholar] [CrossRef] [PubMed]
  34. Franchignoni, F.; Horak, F.; Godi, M.; Nardone, A.; Giordano, A. Using Psychometric Techniques to Improve the Balance Evaluation Systems Test: The Mini-Bestest. J. Rehabil. Med. 2010, 42, 323–331. [Google Scholar] [CrossRef]
  35. El-Gohary, M.; Peterson, D.; Gera, G.; Horak, F.B.; Huisinga, J.M. Validity of the Instrumented Push and Release Test to Quantify Postural Responses in Persons with Multiple Sclerosis. Arch. Phys. Med. Rehabil. 2017, 98, 1325–1331. [Google Scholar] [CrossRef]
  36. Morris, A.; Fino, N.F.; Pelo, R.; Kreter, N.; Cassidy, B.; Dibble, L.E.; Fino, P.C. Interadministrator Reliability of a Modified Instrumented Push and Release Test of Reactive Balance. J. Sport Rehabil. 2022, 31, 517–523. [Google Scholar] [CrossRef]
  37. Morris, A.; Petersell, T.L.; Pelo, R.; Hill, S.; Cassidy, B.; Jameson, T.; Iriye, T.; Burke, J.; Dibble, L.E.; Fino, P.C. Use of Reactive Balance Assessments With Clinical Baseline Concussion Assessments in Collegiate Athletes. J. Athl. Train. 2024, 59, 39–48. [Google Scholar] [CrossRef]
  38. Morris, A.; Cassidy, B.; Pelo, R.; Fino, N.F.; Presson, A.P.; Cushman, D.M.; Monson, N.E.; Dibble, L.E.; Fino, P.C. Reactive Postural Responses After Mild Traumatic Brain Injury and Their Association With Musculoskeletal Injury Risk in Collegiate Athletes: A Study Protocol. Front. Sports Act. Living 2020, 2, 574848. [Google Scholar] [CrossRef]
  39. Takla, T.N.; Monaghan, P.G.; Peterson, D.S.; Fritz, N.E. The Relation Among Reactive Stepping and Fall-Related Psychological Factors in Multiple Sclerosis. Brain Sci. 2024, 14, 1197. [Google Scholar] [CrossRef]
  40. Fitbit How Does My Fitbit Device Calculate Active Minutes? Available online: https://help.fitbit.com/articles/en_US/Help_article/1379.htm (accessed on 6 February 2024).
  41. Fitbit How Does My Fitbit Device Calculate Calories Burned? Available online: https://support.google.com/fitbit/answer/14237111?hl=en#zippy=%2Chow-does-my-fitbit-device-calculate-calories-burned (accessed on 6 February 2024).
  42. Block, V.J.; Zhao, C.; Hollenbach, J.A.; Olgin, J.E.; Marcus, G.M.; Pletcher, M.J.; Henry, R.; Gelfand, J.M.; Cree, B.A.C. Validation of a Consumer-Grade Activity Monitor for Continuous Daily Activity Monitoring in Individuals with Multiple Sclerosis. Mult. Scler. J. Exp. Transl. Clin. 2019, 5, 2055217319888660. [Google Scholar] [CrossRef]
  43. Reid, R.E.R.; Insogna, J.A.; Carver, T.E.; Comptour, A.M.; Bewski, N.A.; Sciortino, C.; Andersen, R.E. Validity and Reliability of Fitbit Activity Monitors Compared to ActiGraph GT3X+ with Female Adults in a Free-Living Environment. J. Sci. Med. Sport 2017, 20, 578–582. [Google Scholar] [CrossRef] [PubMed]
  44. Motl, R.W.; Zhu, W.; Park, Y.; McAuley, E.; Scott, J.A.; Snook, E.M. Reliability of Scores from Physical Activity Monitors in Adults with Multiple Sclerosis. Adapt. Phys. Act. Q. 2007, 24, 245–253. [Google Scholar] [CrossRef]
  45. Dasmahapatra, P.; Chiauzzi, E.; Bhalerao, R.; Rhodes, J. Free-Living Physical Activity Monitoring in Adult US Patients with Multiple Sclerosis Using a Consumer Wearable Device. Digit. Biomark. 2018, 2, 47–63. [Google Scholar] [CrossRef]
  46. Polhemus, A.; Sieber, C.; Haag, C.; Sylvester, R.; Kool, J.; Gonzenbach, R.; von Wyl, V. Non-Equivalent, but Still Valid: Establishing the Construct Validity of a Consumer Fitness Tracker in Persons with Multiple Sclerosis. PLoS Digit. Health 2023, 2, e0000171. [Google Scholar] [CrossRef] [PubMed]
  47. Chu, A.H.Y.; Ng, S.H.X.; Paknezhad, M.; Gauterin, A.; Koh, D.; Brown, M.S.; Müller-Riemenschneider, F. Comparison of Wrist-Worn Fitbit Flex and Waist-Worn ActiGraph for Measuring Steps in Free-Living Adults. PLoS ONE 2017, 12, e0172535. [Google Scholar] [CrossRef] [PubMed]
  48. Akaike, H. A New Look at the Statistical Model Identification. IEEE Trans. Autom. Control 1974, 19, 716–723. [Google Scholar] [CrossRef]
  49. Kalb, R.; Brown, T.R.; Coote, S.; Costello, K.; Dalgas, U.; Garmon, E.; Giesser, B.; Halper, J.; Karpatkin, H.; Keller, J.; et al. Exercise and Lifestyle Physical Activity Recommendations for People with Multiple Sclerosis throughout the Disease Course. Mult. Scler. J. 2020, 26, 1459–1469. [Google Scholar] [CrossRef]
  50. Dlugonski, D.; Pilutti, L.A.; Sandroff, B.M.; Suh, Y.; Balantrapu, S.; Motl, R.W. Steps per Day among Persons with Multiple Sclerosis: Variation by Demographic, Clinical, and Device Characteristics. Arch. Phys. Med. Rehabil. 2013, 94, 1534–1539. [Google Scholar] [CrossRef]
  51. Motl, R.W.; McAuley, E. Pathways Between Physical Activity and Quality of Life in Adults with Multiple Sclerosis. Health Psychol. 2009, 28, 682–689. [Google Scholar] [CrossRef]
  52. Learmonth, Y.C.; Motl, R.W. Physical Activity and Exercise Training in Multiple Sclerosis: A Review and Content Analysis of Qualitative Research Identifying Perceived Determinants and Consequences. Disabil. Rehabil. 2016, 38, 1227–1242. [Google Scholar] [CrossRef]
  53. Snook, E.M.; Motl, R.W. Physical Activity Behaviors in Individuals with Multiple Sclerosis: Roles of Overall and Specific Symptoms, and Self-Efficacy. J. Pain. Symptom Manag. 2008, 36, 46–53. [Google Scholar] [CrossRef] [PubMed]
  54. Kasser, S.L.; Jacobs, J.V.; Littenberg, B.; Foley, J.T.; Cardinal, B.J.; Maddalozzo, G.F. Exploring Physical Activity in Women with Multiple Sclerosis: Associations with Fear of Falling and Underlying Impairments. Am. J. Phys. Med. Rehabil. 2014, 93, 461–469. [Google Scholar] [CrossRef]
  55. Gunn, H.; Cameron, M.; Hoang, P.; Lord, S.; Shaw, S.; Freeman, J. Relationship Between Physiological and Perceived Fall Risk in People With Multiple Sclerosis: Implications for Assessment and Management. Arch. Phys. Med. Rehabil. 2018, 99, 2022–2029. [Google Scholar] [CrossRef] [PubMed]
  56. Longhurst, J.K.; Hooyman, A.; Landers, M.R.; Mancini, M.; Franzén, E.; Leavy, B.; Johansson, H.; Peterson, D. Discordance Between Balance Ability and Perception Is Associated With Falls in Parkinson’s Disease: A Coordinated Analysis. Neurorehabil. Neural Repair 2024, 39, 114–125. [Google Scholar] [CrossRef]
  57. Huynh, T.L.T.; Silveira, S.L.; Jeng, B.; Motl, R.W. Association of Disease Outcomes With Physical Activity in Multiple Sclerosis: A Cross-Sectional Study. Rehabil. Psychol. 2022, 67, 421–429. [Google Scholar] [CrossRef]
  58. Sieber, C.; Haag, C.; Polhemus, A.; Haile, S.R.; Sylvester, R.; Kool, J.; Gonzenbach, R.; von Wyl, V. Exploring the Major Barriers to Physical Activity in Persons With Multiple Sclerosis: Observational Longitudinal Study. JMIR Rehabil. Assist. Technol. 2024, 11, e52733. [Google Scholar] [CrossRef] [PubMed]
  59. Neal, W.N.; Cederberg, K.L.; Jeng, B.; Sasaki, J.E.; Motl, R.W. Is Symptomatic Fatigue Associated With Physical Activity and Sedentary Behaviors Among Persons With Multiple Sclerosis? Neurorehabil. Neural Repair 2020, 34, 505–511. [Google Scholar] [CrossRef]
  60. Motl, R.W.; McAuley, E.; Wynn, D.; Suh, Y.; Weikert, M.; Dlugonski, D. Symptoms and Physical Activity among Adults with Relapsing-Remitting Multiple Sclerosis. J. Nerv. Ment. Dis. 2010, 198, 213–219. [Google Scholar] [CrossRef]
  61. Motl, R.W.; Suh, Y.; Weikert, M.; Dlugonski, D.; Balantrapu, S.; Sandroff, B. Fatigue, Depression, and Physical Activity in Relapsing-Remitting Multiple Sclerosis: Results from a Prospective, 18-Month Study. Mult. Scler. Relat. Disord. 2012, 1, 43–48. [Google Scholar] [CrossRef]
  62. Merkelbach, S.; Schulz, H.; Kölmel, H.W.; Gora, G.; Klingelhöfer, J.; Dachsel, R.; Hoffmann, F.; Polzer, U. Fatigue, Sleepiness, and Physical Activity in Patients with Multiple Sclerosis. J. Neurol. 2011, 258, 74–79. [Google Scholar] [CrossRef]
  63. Feys, P.; Gijbels, D.; Romberg, A.; Santoyo, C.; Gebara, B.; De Noordhout, B.M.; Knuts, K.; Béthoux, F.; De Groot, V.; Vaney, C.; et al. Effect of Time of Day on Walking Capacity and Self-Reported Fatigue in Persons with Multiple Sclerosis: A Multi-Center Trial. Mult. Scler. J. 2012, 18, 351–357. [Google Scholar] [CrossRef] [PubMed]
  64. Rietberg, M.B.; Van Wegen, E.E.H.; Uitdehaag, B.M.J.; Kwakkel, G. The Association between Perceived Fatigue and Actual Level of Physical Activity in Multiple Sclerosis. Mult. Scler. J. 2011, 17, 1231–1237. [Google Scholar] [CrossRef] [PubMed]
  65. Enoka, R.M.; Almuklass, A.M.; Alenazy, M.; Alvarez, E.; Duchateau, J. Distinguishing between Fatigue and Fatigability in Multiple Sclerosis. Neurorehabil. Neural Repair 2021, 35, 960–973. [Google Scholar] [CrossRef]
  66. Loy, B.D.; Taylor, R.L.; Fling, B.W.; Horak, F.B. Relationship between Perceived Fatigue and Performance Fatigability in People with Multiple Sclerosis: A Systematic Review and Meta-Analysis. J. Psychosom. Res. 2017, 100, 1–7. [Google Scholar] [CrossRef] [PubMed]
  67. Téllez, N.; Río, J.; Tintoré, M.; Nos, C.; Galán, I.; Montalban, X. Does the Modified Fatigue Impact Scale Offer a More Comprehensive Assessment of Fatigue in MS? Mult. Scler. J. 2005, 11, 198–202. [Google Scholar] [CrossRef]
  68. Motl, R.W.; Sandroff, B.M. Objective Monitoring of Physical Activity Behavior in Multiple Sclerosis. Phys. Ther. Rev. 2010, 15, 204–211. [Google Scholar] [CrossRef]
  69. Peterson, D.S.; Huisinga, J.M.; Spain, R.I.; Horak, F.B. Characterization of Compensatory Stepping in People with Multiple Sclerosis. Arch. Phys. Med. Rehabil. 2016, 97, 513–521. [Google Scholar] [CrossRef]
  70. Monaghan, P.G.; VanNostrand, M.; Fritz, N.E. Backwards Walking Speed Reserve in People with Multiple Sclerosis. Mult. Scler. Relat. Disord. 2024, 85, 105556. [Google Scholar] [CrossRef]
  71. Takla, T.N.; Chargo, A.N.; Daugherty, A.M.; Fritz, N.E. Cognitive Contributors of Backward Walking in Persons with Multiple Sclerosis. Mult. Scler. Int. 2023, 2023, 1–10. [Google Scholar] [CrossRef]
  72. Hackney, M.E.; Earhart, G.M. Backward Walking in Parkinson’s Disease. Mov. Disord. 2009, 24, 218–223. [Google Scholar] [CrossRef]
  73. VanNostrand, M.; Monaghan, P.G.; Fritz, N.E. Examination of Proprioceptive Reliance During Backward Walking in Individuals With Multiple Sclerosis. J. Neurol. Phys. Ther. 2024, 86, 105588. [Google Scholar] [CrossRef]
  74. Edwards, E.M.; Daugherty, A.M.; Nitta, M.; Atalla, M.; Fritz, N.E. Backward Walking Sensitively Detects Fallers in Persons with Multiple Sclerosis. Mult. Scler. Relat. Disord. 2020, 45, 102390. [Google Scholar] [CrossRef]
  75. Klineova, S.; Lublin, F.D. Clinical Course of Multiple Sclerosis. Cold Spring Harb. Perspect. Med. 2018, 8, a028928. [Google Scholar] [CrossRef] [PubMed]
  76. Boeschoten, R.E.; Braamse, A.M.J.; Beekman, A.T.F.; Cuijpers, P.; van Oppen, P.; Dekker, J.; Uitdehaag, B.M.J. Prevalence of Depression and Anxiety in Multiple Sclerosis: A Systematic Review and Meta-Analysis. J. Neurol. Sci. 2017, 372, 331–341. [Google Scholar] [CrossRef] [PubMed]
  77. Kwon, S.; Han, K.-D.; Jung, J.H.; Cho, E.B.; Chung, Y.H.; Park, J.; Choi, H.L.; Jeon, H.J.; Shin, D.W.; Min, J.-H. Risk of Depression and Anxiety in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorder: A Nationwide Cohort Study in South Korea. Mult. Scler. J. 2024, 30, 714–725. [Google Scholar] [CrossRef]
  78. Marrie, R.A.; Reingold, S.; Cohen, J.; Stuve, O.; Trojano, M.; Sorensen, P.S.; Cutter, G.; Reider, N. The Incidence and Prevalence of Psychiatric Disorders in Multiple Sclerosis: A Systematic Review. Mult. Scler. J. 2015, 21, 305–317. [Google Scholar] [CrossRef]
  79. Carotenuto, A.; Scandurra, C.; Costabile, T.; Lavorgna, L.; Borriello, G.; Moiola, L.; Inglese, M.; Trojsi, F.; Petruzzo, M.; Ianniello, A.; et al. Physical Exercise Moderates the Effects of Disability on Depression in People with Multiple Sclerosis during the COVID-19 Outbreak. J. Clin. Med. 2021, 10, 1234. [Google Scholar] [CrossRef]
Figure 1. Organizational outline summarizing results from three regression models predicting 3-month total step counts, evaluated using the Akaike Information Criterion (AIC) for goodness of fit. Model 1 included participant-reported outcomes alone, model 2 used sensor-derived clinical measures, and model 3 combined participant-reported outcomes with sensor-derived clinical measures. The best-fitting model (model 3) explained 43% of the variance in 3-month step counts by integrating both participant-reported and clinical measures. Abbreviations: MSWS-12, 12-Item Multiple Sclerosis Walking Scale; BW, backward walking; FW, forward walking; FES-I, Fall Efficacy Scale-International; MFIS, Modified Fatigue Impact Scale; PAR, Push and Release Reactive Balance Assessment; ECFT, eyes closed feet together sway condition; and AIC, Akaike Information Criterion.
Figure 1. Organizational outline summarizing results from three regression models predicting 3-month total step counts, evaluated using the Akaike Information Criterion (AIC) for goodness of fit. Model 1 included participant-reported outcomes alone, model 2 used sensor-derived clinical measures, and model 3 combined participant-reported outcomes with sensor-derived clinical measures. The best-fitting model (model 3) explained 43% of the variance in 3-month step counts by integrating both participant-reported and clinical measures. Abbreviations: MSWS-12, 12-Item Multiple Sclerosis Walking Scale; BW, backward walking; FW, forward walking; FES-I, Fall Efficacy Scale-International; MFIS, Modified Fatigue Impact Scale; PAR, Push and Release Reactive Balance Assessment; ECFT, eyes closed feet together sway condition; and AIC, Akaike Information Criterion.
Sensors 25 01780 g001
Figure 2. Organizational outline summarizing results from three regression models predicting 3-month total physical activity, evaluated using the Akaike Information Criterion (AIC) for goodness of fit. Model 1 included participant-reported outcomes alone, model 2 used sensor-derived clinical measures, and model 3 combined participant-reported outcomes with sensor-derived clinical measures. The best-fitting model (model 3) explained 43% of the variance in 3-month total physical activity by integrating both participant-reported and clinical measures. Abbreviations: MSWS-12, 12-Item Multiple Sclerosis Walking Scale; BW, backward walking; FW, forward walking; FES-I, Fall Efficacy Scale-International; MFIS, Modified Fatigue Impact Scale; PAR, Push and Release Reactive Balance Assessment; ECFT, eyes closed feet together sway condition; and AIC, Akaike Information Criterion.
Figure 2. Organizational outline summarizing results from three regression models predicting 3-month total physical activity, evaluated using the Akaike Information Criterion (AIC) for goodness of fit. Model 1 included participant-reported outcomes alone, model 2 used sensor-derived clinical measures, and model 3 combined participant-reported outcomes with sensor-derived clinical measures. The best-fitting model (model 3) explained 43% of the variance in 3-month total physical activity by integrating both participant-reported and clinical measures. Abbreviations: MSWS-12, 12-Item Multiple Sclerosis Walking Scale; BW, backward walking; FW, forward walking; FES-I, Fall Efficacy Scale-International; MFIS, Modified Fatigue Impact Scale; PAR, Push and Release Reactive Balance Assessment; ECFT, eyes closed feet together sway condition; and AIC, Akaike Information Criterion.
Sensors 25 01780 g002
Table 1. Demographics.
Table 1. Demographics.
Descriptive StatisticsN = 45
Age (years)51.16 ± 11.12
Sex (n, % female)38, 84%
Race (n)White: 23
African American/Black: 21
Native American: 2
Pacific Islander: 1
Hispanic/Chicano: 1
PDDS [median (range)]1 (0–6)
MS Subtype (n, %)RRMS: 42, 93.33%
SPMS: 2, 4.44%
PPMS: 1, 2.22%
Participant-Reported Outcomes
MSWS-1235.69 ± 30.15
FES-I27.20 ± 9.30
MFIS32.71 ± 17.79
Sensor-Derived Clinical Outcomes
BW velocity (m/s)0.65 ± 0.33
FW velocity (m/s)0.99 ± 0.37
PAR time to stabilization (s)1.47 ± 0.64
ECFT sway area (m2/s4)0.38 ± 0.46
3-Month Prospective Physical Activity
Average daily physical activity in minutes 252 ± 93
Average daily step count 5947 ± 3073
Average daily wear time (minutes) (maximum = 1440 min)1299 ± 109
Average daily percentage wear time90.25 ± 7.62%
Note. Three individuals reported two racial groups. PDDS: Patient-Determined Disease Steps; MSWS-12: 12-Item Multiple Sclerosis Walking Scale; BW: backward walking; FW: forward walking; FES-I: Fall Efficacy Scale-International; MFIS: Modified Fatigue Impact Scale; PAR: Push and Release Reactive Balance Assessment; and ECFT: eyes closed feet together sway condition.
Table 2. Correlation matrix.
Table 2. Correlation matrix.
3-Month Step Count3-Month Total ActivityAgePDDSMSWS-12MFISFES-IFW VelocityBW VelocityPAR Time to StabilizationECFT Sway Area
3-Month daily step count -0.75 **−0.26−0.40 **a−0.50 **a−0.27−0.44 **a0.45 **0.57 **−0.27−0.11 a
3-Month daily total activity -−0.11−0.49 **a−0.59 **a−0.26−0.51 **a0.50 **0.54 **−0.23−0.01 a
Age -0.19 a0.18 a−0.050.16 a−0.04−0.200.150.14 a
PDDS -0.87 **a0.60 **a0.62 **a−0.62 **a−0.67 **a0.30 *a0.54 **a
MSWS-12 -0.68 **a0.63 **a−0.65 **a−0.61 **a0.17 a0.41 **a
MFIS -0.55 **a−0.32 *−0.28 *0.210.40 **a
FES-I -−0.56 **a−0.57 **a0.32 *a0.36 **a
FW velocity -0.87 **−0.29 *−0.25 a
BW velocity -−0.28−0.46 **a
PAR time to stabilization -0.27 *a
ECFT sway area -
* Denotes significance p < 0.05; ** denotes significance p < 0.01; and a denotes Spearman’s rank correlation. PDDS: Patient-Determined Disease Steps; MSWS-12: 12-Item Multiple Sclerosis Walking Scale; MFIS: Modified Fatigue Impact Scale; FES-I: Falls Efficacy Scale-International; FW: forward walking; BW: backward walking; PAR: Push and Release Reactive Balance Assessment; and ECFT: eyes closed feet together sway condition.
Table 3. Linear regression results examining contributors to 3-month daily step count.
Table 3. Linear regression results examining contributors to 3-month daily step count.
3-Month Daily Step Count
Model 1 BβTp-value
Age−55.56−0.20−1.450.15
PDDS426.090.281.080.29
MSWS-12−65.32−0.68−2.650.01
R2 0.28
AIC 842.74
p-value <0.01
F-statistic (3,41) 5.29
Model 2 BβTp-value
Age−43.08−0.15−1.190.24
PDDS87.730.060.350.73
BW velocity5383.300.573.44<0.01
R2 0.35
AIC 838.43
p-value <0.01
F-statistic (3,41) 7.20
Model 3 BβTp-value
Age−39.56−0.14−1.250.26
PDDS745.320.492.020.05
MSWS-12−52.980.51−2.340.03
BW velocity4777.85−0.553.17<0.01
R2 0.42
AIC 834.67
p-value <0.01
F-statistic (4,40) 7.35
PDDS: Patient-Determined Disease Steps; MSWS-12: 12-Item Multiple Sclerosis Walking Scale; BW: backward walking; and AIC: Akaike Information Criterion.
Table 4. Linear regression results examining contributors to 3-month daily total activity.
Table 4. Linear regression results examining contributors to 3-month daily total activity.
3-Month Daily Activity Count
Model 1 BβTp-value
Age−0.22−0.03−0.200.84
PDDS8.050.170.700.49
MSWS-12−2.23−0.74−3.08<0.01
R2 0.37
AIC 525.25
p-value <0.01
F-statistic (3,41) 7.98
Model 2 BβTp-value
Age−0.05−0.01−0.040.97
PDDS−10.02−0.21−1.240.22
BW velocity120.340.412.400.02
R2 0.32
AIC 528.70
p-value <0.01
F-statistic (3,41) 6.39
Model 3 BβTp-value
Age0.080.010.080.94
PDDS14.570.301.260.21
MSWS-12−1.98−0.66−2.800.01
BW velocity97.700.332.070.05
R2 0.43
AIC 522.66
p-value <0.01
F-statistic (4,40) 7.54
PDDS: Patient-Determined Disease Steps; MSWS-12: 12-Item Multiple Sclerosis Walking Scale; BW: backward walking; and AIC Akaike Information Criterion.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Monaghan, P.G.; VanNostrand, M.; Takla, T.N.; Fritz, N.E. Predicting Real-World Physical Activity in Multiple Sclerosis: An Integrated Approach Using Clinical, Sensor-Based, and Self-Reported Measures. Sensors 2025, 25, 1780. https://doi.org/10.3390/s25061780

AMA Style

Monaghan PG, VanNostrand M, Takla TN, Fritz NE. Predicting Real-World Physical Activity in Multiple Sclerosis: An Integrated Approach Using Clinical, Sensor-Based, and Self-Reported Measures. Sensors. 2025; 25(6):1780. https://doi.org/10.3390/s25061780

Chicago/Turabian Style

Monaghan, Patrick G., Michael VanNostrand, Taylor N. Takla, and Nora E. Fritz. 2025. "Predicting Real-World Physical Activity in Multiple Sclerosis: An Integrated Approach Using Clinical, Sensor-Based, and Self-Reported Measures" Sensors 25, no. 6: 1780. https://doi.org/10.3390/s25061780

APA Style

Monaghan, P. G., VanNostrand, M., Takla, T. N., & Fritz, N. E. (2025). Predicting Real-World Physical Activity in Multiple Sclerosis: An Integrated Approach Using Clinical, Sensor-Based, and Self-Reported Measures. Sensors, 25(6), 1780. https://doi.org/10.3390/s25061780

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop