Next Article in Journal
Automated Monitoring of Human–Computer Interaction for Assessing Teachers’ Digital Competence Based on LMS Data Extraction
Next Article in Special Issue
The Reliability and Validity of the OneStep Smartphone Application for Gait Analysis among Patients Undergoing Rehabilitation for Unilateral Lower Limb Disability
Previous Article in Journal
Validation of Inertial-Measurement-Unit-Based Ex Vivo Knee Kinematics during a Loaded Squat before and after Reference-Frame-Orientation Optimisation
Previous Article in Special Issue
A Statistical and AI Analysis of the Frequency Spectrum in the Measurement of the Center of Pressure Track in the Seated Position in Healthy Subjects and Subjects with Low Back Pain
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Communication

Testing Dynamic Balance in People with Multiple Sclerosis: A Correlational Study between Standard Posturography and Robotic-Assistive Device

1
Italian Multiple Sclerosis Foundation, 16149 Genoa, Italy
2
Movendo Technology S.R.L, 16149 Genoa, Italy
3
Department of Experimental Medicine, University of Genoa, 16126 Genoa, Italy
4
AISM Rehabilitation Service, 16149 Genoa, Italy
*
Author to whom correspondence should be addressed.
Sensors 2024, 24(11), 3325; https://doi.org/10.3390/s24113325
Submission received: 30 April 2024 / Revised: 17 May 2024 / Accepted: 21 May 2024 / Published: 23 May 2024
(This article belongs to the Special Issue Advanced Sensors in Biomechanics and Rehabilitation)

Abstract

:
Background: Robotic devices are known to provide pivotal parameters to assess motor functions in Multiple Sclerosis (MS) as dynamic balance. However, there is still a lack of validation studies comparing innovative technologies with standard solutions. Thus, this study’s aim was to compare the postural assessment of fifty people with MS (PwMS) during dynamic tasks performed with the gold standard EquiTest® and the robotic platform hunova®, using Center of Pressure (COP)-related parameters and global balance indexes. Methods: Pearson’s ρ correlations were run for each COP-related measure and the global balance index was computed from EquiTest® and hunova® in both open (EO) and closed-eyes (EC) conditions. Results: Considering COP-related parameters, all correlations were significant in both EO (0.337 ≤ ρ ≤ 0.653) and EC (0.344 ≤ ρ ≤ 0.668). Furthermore, Pearson’s analysis of global balance indexes revealed relatively strong for visual and vestibular, and strong for somatosensory system associations (ρ = 0.573; ρ = 0.494; ρ = 0.710, respectively). Conclusions: Findings confirm the use of hunova® as a valid device for dynamic balance assessment in MS, suggesting that such a robotic platform could allow for a more sensitive assessment of balance over time, and thus a better evaluation of the effectiveness of personalized treatment, thereby improving evidence-based clinical practice.

1. Introduction

Balance impairment is a major issue in Multiple Sclerosis (MS) leading to an increased risk of falling [1] that often prevents people with MS (PwMS) from performing their daily living activities [2,3], with a negative impact on their quality of life [4]. When compared to healthy controls of similar age, PwMS experience more falls as a result of these impairments [5]. Indeed, a meta-analysis on falls in MS showed that 56% of PwMS fall at least once per 3 months [6]. Central nervous system damage, observed in PwMS, leads to an altered central sensory integration of signals from muscle, tendon, joint proprioceptors, skin exteroceptors, and vestibular and visual inputs affecting postural response to maintain correct balance [7]. As indicated by Cameron and Nilsagård (2013), PwMS often present three main balance control abnormalities: decreased ability to maintain position when attempting to stand still; limited and slowed movement toward their limits of stability when attempting to lean or reach; and delayed automatic postural responses when displaced or perturbed [8]. Therefore, an accurate balance assessment is highly recommended for clinical practice and research as a key factor to monitor disease progression and tailor rehabilitative interventions. Extensive research has examined the contributions of physiological impairments to static balance [9,10,11,12,13], but falls most frequently occur during dynamic activities, such as walking or when surfaces are unstable [14,15]. The importance of assessing dynamic balance has been further highlighted by Anastasi and colleagues (2023): maintaining a stable gait requires high levels of motor control to integrate sensorimotor information about the position and the velocity of the Center of Mass (CoM); stabilize and redirect the CoM and provide an adequate foot placement at each step [1]. To this aim, several dynamic balance assessment tools have been developed, including clinical scales, such as the Fullerton Advanced Balance Scale (FAB) [16]. However, this scale has been shown to be suitable mainly for PwMS with low disability [17]. Other measures such as the Time Up and Go (TUG) [18] and the modified Dynamic Gait Index (DGI) [19] are common tests used to qualitatively and quantitatively assess instability during walking in PwMS, although they suffer from partial subjectivity, and poor sensitivity to change [1]. Given the need for a high-quality (precise, reliable, and valid) assessment of postural dynamic stability, additional balance assessment devices can be helpful in MS clinical settings. To overcome the aforementioned limitations of clinical scales and tests, posturography can provide valuable information about the individual’s postural stability, including the ability to maintain balance in different sensory conditions [12]. Kasser and colleagues (2011) [15] also demonstrated that reduced limits of stability on voluntary movement during dynamic posturography accurately identified frequent fallers in a sample of women with MS. However, to date, one of the gold standards in dynamic posturography, EquiTest® (NeuroCom International, Inc., Clackamas, OR, USA) [20], presents some boundaries that limit its use in a clinical context (e.g., its reliance is limited only on an antero-posterior plane) [21]. Thus, in recent years, an increased number of new technologies, such as robotic-assistive systems, have been developed to provide a precise and complete assessment of balance in the neurological population, thanks to novel computational approaches as well as sophisticated electronic components [22]. Thus, investigating the correlation between conventional technology-driven performance assessments and innovative robotic methods for evaluating balance could be of utmost relevance in both MS clinical practice and research [23]. A recent study by Podda and colleagues (2023) confirms that a robotic platform can constitute an important innovative adjunct to balance assessment for PwMS [10]. In this study, authors compared the postural assessment during static tasks performed with an advanced robotic system and a standard posturography in a standing position [10]. Results indicated that robotic and standard outcomes strongly correlated considering Center Of Pressure (COP)-balance parameters and composite indexes calculated as global measures of balance. However, static balance assessment is usually performed in circumstances that are somewhat away from those encountered in daily-life scenarios. Since dynamic conditions, known to be more challenging than static ones, could provide more meaningful and ecological information on balance in MS, the aim of the present study was to investigate whether the postural assessment during dynamic tasks performed with hunova® (Movendo Technology, SRL. Genoa, Italy) was comparable with the gold standard EquiTest® [24] (NeuroCom International, Inc., Clackamas, OR, USA in a sample of PwMS.

2. Materials and Methods

2.1. Balance Assessment

Balance assessment was performed with both the EquiTest® and hunova® (See Figure 1). In particular, the sensory organization test (SOT) from EquiTest® [24] and the Balance Test (BT) from hunova® [25] were administered to measure balance (please see Supplementary Materials for an overview of both devices and their assessments).
The SOT is a six-condition assessment able to isolate and quantify impairments in the patient’s use of somatosensory, visual, and vestibular inputs to maintain balance, and impairments related to the patient’s use of specific sensory input when it is incorrect or unavailable [24]. In conditions 1 and 2 (COND 1 and COND 2), the participant stands quietly with eyes open (EO) and closed (EC), respectively; in both conditions, the platform and visual surround are fixed. In condition 3 (COND 3), the participant stands with EO; the platform is fixed, and the visual surround is sway-referenced (i.e., sway referencing refers to movement of the platform and/or visual surround in response to the body’s own sway, typically in an anterior-posterior direction). In condition 4 (COND 4), performed with EO, the support surface is sway-referenced whereas the surround is fixed. Condition 5 (COND 5) is performed with EC and a sway-referenced support surface, while the surround is fixed. Finally, in condition 6 (COND 6), the participant stands with EO; the visual surround and support surface are both sway-referenced. Each condition consists of three trials of 20 s. Scores are reported out of a maximum score of 100, indicating perfect balance and absence of sway. In addition to scores reported for each condition, there is also a composite score that represents all scores, with heavier weighting on those conditions that rely more heavily on the use of vestibular cues alone. Performances are evaluated using the Equilibrium Score that quantifies postural stability during each of the three trials of the six SOT conditions (see [10] for details on the computation).
Designed as a robotic aid for healthcare professionals that is intuitive and easy to use, the use of hunova® in different clinical settings such as neurology, orthopedics, and geriatrics is enlarging and has been validated in several studies and clinical trials with promising results [26,27,28,29]. BT on hunova® allows testing balance under different conditions. More precisely, the device can simulate a static environment, or it can operate in a passive, an active, and an assistive modality. In the passive modality, the movements of the platforms are pre-planned following given trajectories with different speed levels. In the active modality, the user can actively move the platforms while it exerts a certain selectable resistance. When the assistive modality is selected, the device completes the exercise when subjects are unable to do it independently [30]. First, participants’ static balance was assessed with both devices in order to confirm previous results [10]. Static balance was tested with COND 1 and COND 2 of SOT for EquiTest® and with two trials of BT performed with hunova® on a static platform (s-BT) with both EO and EC. Then, dynamic balance was assessed using the COND 4 and COND 5 of the SOT and two trials of the elastic task of the BT (e-BT) performed on the unstable platform of hunova® with both EO and EC. In e-BT, PwMS were asked to stand still on the unstable surface, which tilted in response to the weight shift of the subject. The platform responded as a plate on a pivot, with an additional low elastic rotatory force field that opposed the movement induced by the subject weight shift and tended to restore the platform parallel to the floor [25]. Figure 2 shows platforms from each device.
In both EquiTest® and hunova®, participants were required to stand upright, with their arms relaxed along the sides of the body, looking straight ahead and avoid moving their feet for the entire duration of the test. The duration of the entire balance assessment was 30 min (EquiTest®: 20 min, hunova®: 10 min). The order of assessment delivered with EquiTest® and hunova® was counterbalanced between participants (see Figure 3 for a flow chart of the study).

2.1.1. COP-Related Balance Measures

For both static and dynamic assessments, the following COP-related balance measures were calculated: sway area (SA) (cm2), Medio-Lateral (ML) and Anterior-Posterior (AP) oscillation range (cm), total path length (cm), ML and AP speed (cm/s), ML and AP root mean squared (RMS) distance (cm) [11]. While hunova® easily provides these measures to the user, the same outcomes were not directly available for the EquiTest® and thus were computed from raw data. All these measures are proportional to the instability of the individuals: the greater the values, the lesser the individual capability to maintain balance.

2.1.2. Global Balance Indexes

From the average of the Equilibrium Scores of each condition, the sensory analysis was run to compute balance global scores such as SOM, calculated as COND 2/COND 1 (if under the normative threshold, it suggests the presence of a somatosensory impairment); VIS, as COND 4/COND 1 (if under the normative threshold, it suggests the inability to use vision for compensatory purposes); and VEST, as COND 5/COND 1 (if under the normative threshold, it suggests a possible vestibular deficit).
Although, by default, hunova® does not directly compute the Equilibrium Score and, consequently, does not perform the sensory analysis, the aforementioned global parameters (SOM, VIS, and VEST) were calculated from the SA values. More precisely, the following equations were computed:
S O M B T = S A E C   o f   s B T S A E O   o f   s B T
SOM represents the ratio of the SA of both EC and EO for s-BT;
V I S B T = S A E O   o f   e B T S A E O   o f   s B T
VIS is the ratio of the SA of EO of e-BT to the SA of EO of s-BT;
V E S T B T = S A E C   o f   e B T S A E O   o f   s B T
Finally, VEST reflects the ratio of the SA of EC of e-BT to the SA of EO of s-BT.

2.2. Participants

PwMS were enrolled from those followed as outpatients at the AISM Rehabilitation Service of Genoa (Italy). Inclusion criteria were MS diagnosis according to revised McDonald criteria [31], age between 18 and 75 years, relapsing-remitting (RR) course, a disability level as measured by the Expanded Disability Status Scale (EDSS) [32] ≤6, stable phase of disease without relapses or worsening in the last three months, Berg Balance Score (BBS) [33] score > 35 indicating ability to stand upright and walking with at least one support, and normal cognitive functioning as indicated by a Montreal Cognitive Assessment (MoCA) [34,35] score ≥ 24. We excluded participants with psychiatric disorders, significant visual impairment defined as a Visual System scoring more than 2 at the Functional Systems Score of EDSS, and cardiovascular and/or respiratory disorders. Study procedures and consent forms conformed to the ethical standards of the 2013 revised Declaration of Helsinki and were approved by the regional ethical committee (Comitato Etico Regionale (CER) Liguria, reference number: 36/2022—DB id 12144). All the participants provided written informed consent to participate in the study and to state their agreement with the publication and communication of the results.

2.3. Statistical Analysis

To analyze sample demographic and clinical characteristics, main descriptive statistics (mean, standard deviation) were calculated. Data analysis was based on the raw data recorded during the static and dynamic trials executed with EquiTest® and hunova®. Pearson’s ρ correlation was computed for each COP-related outcome and global balance index from EquiTest® and hunova®. Correlation coefficients ranging from 0.20 to 0.39 were considered as moderate, from 0.40 to 0.59 as relatively strong, from 0.60 to 0.79 as strong, and higher as very strong correlation [36,37]. All p values were two-tailed and statistical significance was defined by alpha error < 0.05. All the algorithms for the calculus of the outcome measures were performed using MATLAB (MathWorks, Natick, MA, USA). Statistical analysis was performed with IBM SPSS Statistics software, 23.0.

3. Results

A total of 50 PwMS (32 females; mean age 52.9 ± 10.44 years; height: 166.76 ± 10.48 cm) were recruited for the study. Clinical characteristics showed a mean EDSS of 3.92 ± 1.38 and a mean disease duration of 12.22 ± 8.79 years. The BBS score was 49.49 ± 5.27 and the Ambulation Index score was 8.19 ± 3.64.

3.1. COP-Related Balance Measures Correlation

Table 1 presents mean values and relative standard deviations for each parameter computed for both EquiTest® and hunova®, as well as the results of the correlation analysis on static balance data (See Figure 4 for a graphical representation of results). All correlations were significantly strong and relatively strong for both EO and EC conditions; only the APO range with EO was moderate. Findings confirmed previous results from [10].
Concerning dynamic tasks, correlations between the two devices aligned with those found for static balance (Table 2). All the correlations were significant and relatively strong or strong for both EO and EC conditions; only the MLO range with both EO and EC was moderate (See Figure 5 for a graphical representation of results).

3.2. Global Balance Indexes Correlation

The results of the correlations between devices on global balance revealed relatively strong correlations for VIS and VEST (ρ = 0.573 and ρ = 0.494, respectively), and strong for SOM (ρ = 0.710) (Table 3).

4. Discussion

In this study, we compared the dynamic balance assessment performed with hunova®, a robotic medical device, and EquiTest®, the gold standard for postural assessment, in a sample of PwMS. Globally, our findings demonstrate the use of hunova® as a valid and reliable device for balance assessment in MS, as well as for dynamic tasks. Here, as a first step towards the aim, we confirmed results from the previous study by Podda and colleagues [10] that found that hunova® measures were highly comparable to those from EquiTest® for static balance in PwMS. Then, considering dynamic balance, the COP-related measures extracted from the raw data significantly correlated, showing moderate to strong associations in both EO (0.337 ≤ ρ ≤ 0.653) and EC (0.344 ≤ ρ ≤ 0.668). In addition, the correlation analysis on global balance indexes led to remarkable results for SOM (ρ = 0.710), VIS (ρ = 0.573), and VEST (ρ = 0.494). This is in line with Tacchino and colleagues [38], who recently demonstrated that both VEST and VIS systems correlated with the Six-Spot-Step-Test, a timed measure of the participant’s ability to maintain balance while challenging their stability during walking [39]. Authors suggest that people with problems in the organization and integration of information from multiple sensory systems involved in balance maintenance could have difficulty in safely navigating through environments with conflicting visual surroundings information, surface changes/irregularities, or obstacles on the ground. In our study, while the strong association for the SOM was expected, as this metric compared the static performance in EC and EO, the other strong correlations were unexpected, given that VIS and VEST indexes may reflect also structural and mechanical differences between the two devices. Indeed, COND 4 and COND 5 of the SOT from the EquiTest® and the e-BT of hunova® are not exactly calculated in the same way. Despite in these conditions the platform of each device moves accordingly to the subject’s sway shift, with movements proportional to the oscillation of the subject, the support surface of the EquiTest® moves only in the AP direction, while hunova® allows for movements in all directions (both AP, ML, and a combination of the two). This is further confirmed by the results from COP-related measures, in which APO and MLO correlations in EO (ρ = 0.506; ρ = 0.337) reflected differences in the ranges of maximum oscillations of the two devices. Dynamic balance disorders are more evident in the ML than in the AP direction, in accordance with the view that ML stabilization is critical for walking [1] and that any deficit in ML postural control is more alarming in MS given that falls to the side are more likely to cause hip fractures [40]. Healthy adults often compensate for a loss of balance due to unexpected ML perturbations with a variety of strategies, such as a lateral ankle strategy (i.e., using an inversion moment that quickly moves the center of pressure to the outer limit of the foot to compensate for medial perturbations) or a hip strategy (i.e., a hip abduction moment to assist in maintaining balance by counteracting the gravitational moment) [41]. As indicated by Anastasi and colleagues (2023) [1], the Margin of Stability (MoS) in the ML direction may be more sensitive than MoS in AP in describing balance disorders in PwMS with moderate to severe disability. Higher ML sway may reflect a “degrees of freedom” problem [40]: with fewer muscles involved in controlling ML motion compared to AP, PwMS may have greater difficulty in adequately activating the hip abductor/adductor muscles to maintain balance [42]. Therefore, it can be reasonable to conclude that e-BT from hunova® is able to simulate common postural disturbances that PwMS experience in their lives (e.g., standing on a bus, slipping on a slippery surface, and falling due to a sudden boost), while EquiTest®, missing perturbations in ML direction, only gave an incomplete view within balance assessment of PwMS. This suggests that a robotic device such as hunova® that considers both AP and ML directions (and its combination) should be recommended since detailed clinical testing may give important guidance in the prevention and rehabilitation of balance disorders in PwMS.
Our findings provide further support for the use of such robotic devices as additional or even in substitution for standard posturography in the MS population. Other than reliance only on AP direction, the safety harness in EquiTest®, fixed to the safety bar, which prevents users from falling, tends to independently stabilize participants’ posture as their COG approaches the limits of stability [10].
In discussing our data, some important limitations need to be considered. Participants’ characteristics may limit the interpretation of our results. The study sample was constituted of individuals able to walk with at least one walking aid (EDSS ≤ 6). Therefore, results may not generalize to individuals with MS with a higher disability level who require two walking aids such as a pair of canes or crutches (EDSS = 6.5). In addition, future studies should evaluate the responsiveness or sensitivity to balance change, investigating the potential of hunova® as an integrated device for both assessment and rehabilitation purposes for PwMS.
To conclude, hunova® could allow for a more sensitive assessment of dynamic balance over time as the disease progresses, and thus a better evaluation of the effectiveness of tailored treatment for everyone, thereby improving evidence-based clinical practice in MS. Furthermore, our findings suggested the importance of a detailed assessment of dynamic balance through sophisticated robotic devices able to closely resemble daily living challenging activities, such as standing or walking on instable surfaces.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/s24113325/s1. The supporting information includes an overview of EquiTest® and hunova® and their balance assessments.

Author Contributions

Conceptualization, J.P.; methodology, J.P., G.M., A.D.L., V.S., and A.T.; software, J.P. and G.M.; formal analysis, G.M.; investigation, A.B.; validation, L.P.; resources, A.B.; data curation, J.P.; writing—original draft preparation, J.P.; writing—review and editing, J.P., G.M., and A.T.; manuscript revision, all; visualization, J.P.; supervision, J.P.; project administration, J.P., A.T., and G.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the European Union—NextGenerationEU, the Ministry of University and Research (MUR), and the National Recovery and Resilience Plan (NRRP), Mission 4, Component 2, Investment 1.5, project “RAISE -Robotics and AI for Socio-economic Empowerment” (ECS00000035).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the regional ethical committee (Comitato Etico Regionale (CER) Liguria, reference number: 36/2022—DB id 12144).

Informed Consent Statement

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

Data Availability Statement

Data will be available on demand, from the corresponding author. The data are not publicly available due to privacy reasons.

Acknowledgments

This study has been carried on and funded by the European Union—NextGenerationEU, the Ministry of University and Research (MUR), and the National Recovery and Resilience Plan (NRRP), Mission 4, Component 2, Investment 1.5, project “RAISE -Robotics and AI for Socio-economic Empowerment” (ECS00000035). JP, GM, ADL, VS, AT, LP, and GB are part of the RAISE Innovation Ecosystem. Furthermore, we would like to thank all the people with MS followed as outpatients at the Rehabilitation Service of Genoa of the Italian MS Society (AISM) for their participation in this research. A special thanks to Maria Madera and Giulia Bignone for their help in patients’ planning evaluations.

Conflicts of Interest

V.S. and A.D.L. used to work, while G.M. is currently working at Movendo Technology, which developed hunova®. Other authors declare that they have no competing interests.

References

  1. Anastasi, D.; Lencioni, T.; Carpinella, I.; Castagna, A.; Crippa, A.; Gervasoni, E.; Corrini, C.; Marzegan, A.; Rabuffetti, M.; Ferrarin, M.; et al. Dynamic Balance during Walking in People with Multiple Sclerosis: A Cross-Sectional Study. Proc. Inst. Mech. Eng. Part H J. Eng. Med. 2023, 237, 199–208. [Google Scholar] [CrossRef] [PubMed]
  2. Halabchi, F.; Alizadeh, Z.; Sahraian, M.A.; Abolhasani, M. Exercise Prescription for Patients with Multiple Sclerosis; Potential Benefits and Practical Recommendations. BMC Neurol. 2017, 17, 185. [Google Scholar] [CrossRef]
  3. Sosnoff, J.J.; Socie, M.J.; Boes, M.K.; Sandroff, B.M.; Pula, J.H.; Suh, Y.; Weikert, M.; Balantrapu, S.; Morrison, S.; Motl, R.W. Mobility, Balance and Falls in Persons with Multiple Sclerosis. PLoS ONE 2011, 6, 2–6. [Google Scholar] [CrossRef]
  4. Matsuda, P.N.; Shumway-Cook, A.; Ciol, M.A.; Bombardier, C.H.; Kartin, D.A. Understanding Falls in Multiple Sclerosis: Association of Mobility Status, Concerns about Falling, and Accumulated Impairments. Phys. Ther. 2012, 92, 407–415. [Google Scholar] [CrossRef] [PubMed]
  5. Ayvat, E.; Doğan, M.; Ayvat, F.; Kılınç, Ö.O.; Sütçü, G.; Kılınç, M.; Yıldırım, S.A. Usefulness of the Berg Balance Scale for Prediction of Fall Risk in Multiple Sclerosis. Neurol. Sci. 2024, 45, 2801–2805. [Google Scholar] [CrossRef] [PubMed]
  6. Nilsagård, Y.; Gunn, H.; Freeman, J.; Hoang, P.; Lord, S.; Mazumder, R.; Cameron, M. Falls in People with MS--an Individual Data Meta-Analysis from Studies from Australia, Sweden, United Kingdom and the United States. Mult. Scler. 2015, 21, 92–100. [Google Scholar] [CrossRef] [PubMed]
  7. Brichetto, G.; Piccardo, E.; Pedullà, L.; Battaglia, M.A. Tailored Balance Exercises on People with Multiple Sclerosis: A Pilot Randomized, Controlled Study. Mult. Scler. J. 2015, 21, 1055–1063. [Google Scholar] [CrossRef] [PubMed]
  8. Cameron, M.H.; Nilsagård, Y.E. Measurement and Treatment of Imbalance and Fall Risk in Multiple Sclerosis Using the International Classification of Functioning, Disability and Health Model. Phys. Med. Rehabil. Clin. N. Am. 2013, 24, 337–354. [Google Scholar] [CrossRef] [PubMed]
  9. Kalron, A.; Nitzani, D.; Achiron, A. Static Posturography across the EDSS Scale in People with Multiple Sclerosis: A Cross Sectional Study. BMC Neurol. 2016, 16, 70. [Google Scholar] [CrossRef] [PubMed]
  10. Podda, J.; Marchesi, G.; Squeri, V.; De Luca, A.; Bellosta, A.; Pedullà, L.; Konrad, G.; Battaglia, M.A.; Brichetto, G.; Tacchino, A. Standard versus Innovative Robotic Balance Assessment for People with Multiple Sclerosis: A Correlational Study. Eur. J. Med. Res. 2023, 28, 254. [Google Scholar] [CrossRef]
  11. Severini, G.; Straudi, S.; Pavarelli, C.; Da Roit, M.; Martinuzzi, C.; Di Marco Pizzongolo, L.; Basaglia, N. Use of Nintendo Wii Balance Board for Posturographic Analysis of Multiple Sclerosis Patients with Minimal Balance Impairment. J. Neuroeng. Rehabil. 2017, 14, 19. [Google Scholar] [CrossRef] [PubMed]
  12. Prosperini, L.; Ospedaliera, A.; Camillo, S.; Castelli, L. Spotlight on Postural Control in Patients with Multiple Sclerosis. Degener. Neurol. Neuromuscul. Dis. 2018, 8, 25–34. [Google Scholar] [CrossRef] [PubMed]
  13. Cattaneo, D.; Jonsdottir, J. Sensory Impairments in Quiet Standing in Subjects with Multiple Sclerosis. Mult. Scler. 2009, 15, 59–67. [Google Scholar] [CrossRef] [PubMed]
  14. Peebles, A.T.; Bruetsch, A.P.; Lynch, S.G.; Jessie, M.; City, K.; States, U.; States, U.; City, K.; States, U.; Sciences, R.; et al. Dynamic Balance Is Related to Physiological Impairments in Persons With Multiple Sclerosis. Arch. Phys. Med. Rehabil. 2019, 99, 2030–2037. [Google Scholar] [CrossRef] [PubMed]
  15. Kasser, S.L.; Jacobs, J.V.; Foley, J.T.; Cardinal, B.J.; Maddalozzo, G.F. A Prospective Evaluation of Balance, Gait, and Strength to Predict Falling in Women with Multiple Sclerosis. Arch. Phys. Med. Rehabil. 2011, 92, 1840–1846. [Google Scholar] [CrossRef] [PubMed]
  16. Schlenstedt, C.; Brombacher, S.; Hartwigsen, G.; Weisser, B.; Möller, B.; Deuschl, G. Comparing the Fullerton Advanced Balance Scale with the Mini-BESTest and Berg Balance Scale to Assess Postural Control in Patients With Parkinson Disease. Arch. Phys. Med. Rehabil. 2015, 96, 218–225. [Google Scholar] [CrossRef] [PubMed]
  17. Mestanza Mattos, F.G.; Gervasoni, E.; Anastasi, D.; Di Giovanni, R.; Tacchino, A.; Brichetto, G.; Carpinella, I.; Confalonieri, P.; Vercellino, M.; Solaro, C.; et al. Assessing Balance in Non-Disabled Subjects with Multiple Sclerosis: Validation of the Fullerton Advanced Balance Scale. Mult. Scler. Relat. Disord. 2020, 42, 102085. [Google Scholar] [CrossRef] [PubMed]
  18. Sebastião, E.; Sandroff, B.M.; Learmonth, Y.C.; Motl, R.W. Validity of the Timed Up and Go Test as a Measure of Functional Mobility in Persons With Multiple Sclerosis. Arch. Phys. Med. Rehabil. 2016, 97, 1072–1077. [Google Scholar] [CrossRef] [PubMed]
  19. Cattaneo, D.; Regola, A.; Meotti, M. Validity of Six Balance Disorders Scales in Persons with Multiple Sclerosis. Disabil. Rehabil. 2006, 28, 789–795. [Google Scholar] [CrossRef] [PubMed]
  20. NeuroCom International NEUROCOM® INTERNATIONAL, Inc. Balance Manager® Systems Technical Specifications; NeuroCom International NEUROCOM® INTERNATIONAL, Inc.: Clackamas, OR, USA, 2008; Volume 6744, pp. 1–8. [Google Scholar]
  21. Hain, T.C. Moving Platform Posturography Testing: Computerized Dynamic Posturography (CDP). Available online: https://dizziness-and-balance.com/testing/posturography.html (accessed on 22 May 2024).
  22. Feys, P.; Straudi, S. Beyond Therapists: Technology-Aided Physical MS Rehabilitation Delivery. Mult. Scler. J. 2019, 25, 1387–1393. [Google Scholar] [CrossRef] [PubMed]
  23. Grove, C.; Whitney, S.; Hetzel, S.; Heiderscheit, B.; Pyle, M. Validation of a Next-Generation Sensory Organization Test in Adults with and without Vestibular Dysfunction. J. Vestib. Res. 2021, 31, 33–45. [Google Scholar]
  24. Vanicek, N.; King, S.A.; Gohil, R.; Chetter, I.C.; Coughlin, P.A. Computerized Dynamic Posturography for Postural Control Assessment in Patients with Intermittent Claudication. J. Vis. Exp. 2013, 82, e51077. [Google Scholar] [CrossRef] [PubMed]
  25. Marchesi, G.; De Luca, A.; Squeri, V.; De Michieli, L.; Vallone, F.; Pilotto, A.; Leo, A.; Casadio, M.; Canessa, A. A Lifespan Approach to Balance in Static and Dynamic Conditions: The Effect of Age on Balance Abilities. Front. Neurol. 2022, 13, 801142. [Google Scholar] [CrossRef] [PubMed]
  26. Saglia, J.A.; De Luca, A.; Squeri, V.; Ciaccia, L.; Sanfilippo, C.; Ungaro, S.; Michieli, L. De Design and Development of a Novel Core, Balance and Lower Limb Rehabilitation Robot: Hunova®. IEEE Int. Conf. Rehabil. Robot. 2019, 2019, 417–422. [Google Scholar] [CrossRef]
  27. Taglione, E.; Catitti, P.; D’Angelo, M.L.; Squeri, V.; Saglia, J.; Sanfilippo, C.; De Michieli, L. Proprioceptive and Motor Training Using the High Performance Robotic Device Hunova: Protocol of a Randomized, Controlled Trial in Patients with Lower Limb Post-Traumatic Conditions. Ann. Phys. Rehabil. Med. 2018, 61, e497–e498. [Google Scholar] [CrossRef]
  28. Cella, A.; de Luca, A.; Squeri, V.; Parodi, S.; Vallone, F.; Giorgeschi, A.; Senesi, B.; Zigoura, E.; Quispe Guerrero, K.L.; Siri, G.; et al. Development and Validation of a Robotic Multifactorial Fall-Risk Predictive Model: A One-Year Prospective Study in Community-Dwelling Older Adults. PLoS ONE 2020, 15, e0234904. [Google Scholar] [CrossRef] [PubMed]
  29. Castelli, L.; Iacovelli, C.; Loreti, C.; Malizia, A.M.; Ricciardelli, I.B.; Tomaino, A.; Fusco, A.; Biscotti, L.; Padua, L.; Giovannini, S. Robotic-Assisted Rehabilitation for Balance in Stroke Patients (ROAR-S): Effects of Cognitive, Motor and Functional Outcomes. Eur. Rev. Med. Pharmacol. Sci. 2023, 27, 8198–8211. [Google Scholar] [CrossRef] [PubMed]
  30. Movendo Technology. Available online: https://www.movendo.technology/our-products/hunova/?lang=en (accessed on 22 May 2024).
  31. Thompson, A.J.; Banwell, B.L.; Barkhof, F.; Carroll, W.M.; Coetzee, T.; Comi, G.; Correale, J.; Fazekas, F.; Filippi, M.; Freedman, M.S. Diagnosis of Multiple Sclerosis: 2017 Revisions of the McDonald Criteria. Lancet Neurol. 2018, 17, 162–173. [Google Scholar] [CrossRef] [PubMed]
  32. Kurtzke, J.F. Rating Neurologic Impairment in Multiple Sclerosis: An Expanded Disability Status Scale (EDSS). Neurology 1983, 33, 1444. [Google Scholar] [CrossRef]
  33. Berg, K.O.; Wood-Dauphinee, S.L.; Williams, J.I.; Maki, B. Measuring Balance in the Elderly: Validation of an Instrument. Can. J. Public Health 1992, 83 (Suppl. S2), 7–11. [Google Scholar]
  34. Dagenais, E.; Rouleau, I.; Demers, M.; Jobin, C.; Roger, E.; Chamelian, L.; Duquette, P. Value of the MoCA Test as a Screening Instrument in Multiple Sclerosis. Can. J. Neurol. Sci. 2013, 40, 410–415. [Google Scholar] [CrossRef] [PubMed]
  35. Nasreddine, Z.S.; Phillips, N.A.; Bédirian, V.; Charbonneau, S.; Whitehead, V.; Collin, I.; Cummings, J.L.; Chertkow, H. The Montreal Cognitive Assessment, MoCA: A Brief Screening Tool for Mild Cognitive Impairment. J. Am. Geriatr. Soc. 2005, 53, 695–699. [Google Scholar] [CrossRef] [PubMed]
  36. Marchesi, G.; Ballardini, G.; Barone, L.; Giannoni, P.; Lentino, C.; De Luca, A.; Casadio, M. Modified Functional Reach Test: Upper-Body Kinematics and Muscular Activity in Chronic Stroke Survivors. Sensors 2021, 22, 230. [Google Scholar] [CrossRef] [PubMed]
  37. Rea, L.M.; Parker, R.A. Designing and Conducting Survey Research: A Comprehensive Guide; John Wiley & Sons: Hoboken, NJ, USA, 2014; ISBN 1118767039. [Google Scholar]
  38. Tacchino, A.; Skjerbæk, A.G.; Podda, J.; Prada, V.; Bragadin, M.M.; Bergamaschi, V.; Susini, A.; Hvid, L.G.; Pedullà, L.; Brichetto, G. The Role of Sensory Systems in the Association between Balance and Walking in People with Multiple Sclerosis. Mult. Scler. Relat. Disord. 2024, 83, 105440. [Google Scholar] [CrossRef] [PubMed]
  39. Brincks, J.; Callesen, J. Examining the Test-Retest Reliability and Construct Validity of the Six-Spot Step Test in Older Adults with Self-Reported Balance Problems. Clin. Rehabil. 2021, 35, 1478–1487. [Google Scholar] [CrossRef] [PubMed]
  40. Morrison, S.; Rynders, C.A.; Sosnoff, J.J. Deficits in Medio-Lateral Balance Control and the Implications for Falls in Individuals with Multiple Sclerosis. Gait Posture 2016, 49, 148–154. [Google Scholar] [CrossRef] [PubMed]
  41. Small, G.H.; Neptune, R.R. Task-Prioritization and Balance Recovery Strategies Used by Young Healthy Adults during Dual-Task Walking. Gait Posture 2022, 95, 115–120. [Google Scholar] [CrossRef] [PubMed]
  42. Peebles, A.T.; Reinholdt, A.; Bruetsch, A.P.; Lynch, S.G.; Huisinga, J.M. Dynamic Margin of Stability during Gait Is Altered in Persons with Multiple Sclerosis. J. Biomech. 2016, 49, 3949–3955. [Google Scholar] [CrossRef]
Figure 1. Devices used for the balance assessment of PwMS. (A) hunova® from Movendo Technology S.R.L., Genoa, IT. hunova® is a medical robotic device aimed at giving a response to the clinical need for the functional sensory–motor evaluation and rehabilitation of the ankle, lower limbs, and trunk that supports doctors, physiotherapists, and patients throughout assessments, treatments, and recoveries. This device enables the evaluation of balance while standing (both in mono- and bi-podalic configurations) and while sitting, both in static and dynamic testing conditions. (B) EquiTest® from NeuroCom International, Inc., Clackamas, OR, USA. EquiTest® allows the execution of standardized assessment protocols such as the Sensory Organization Test (SOT), Motor Control Test (MCT), and Adaptation Test (ADT) that are standard protocols for the assessment of balance disorders, dizziness, and mobility problems such as in MS.
Figure 1. Devices used for the balance assessment of PwMS. (A) hunova® from Movendo Technology S.R.L., Genoa, IT. hunova® is a medical robotic device aimed at giving a response to the clinical need for the functional sensory–motor evaluation and rehabilitation of the ankle, lower limbs, and trunk that supports doctors, physiotherapists, and patients throughout assessments, treatments, and recoveries. This device enables the evaluation of balance while standing (both in mono- and bi-podalic configurations) and while sitting, both in static and dynamic testing conditions. (B) EquiTest® from NeuroCom International, Inc., Clackamas, OR, USA. EquiTest® allows the execution of standardized assessment protocols such as the Sensory Organization Test (SOT), Motor Control Test (MCT), and Adaptation Test (ADT) that are standard protocols for the assessment of balance disorders, dizziness, and mobility problems such as in MS.
Sensors 24 03325 g001
Figure 2. hunova® (A) and EquiTest® platforms (B).
Figure 2. hunova® (A) and EquiTest® platforms (B).
Sensors 24 03325 g002
Figure 3. Flow chart of the study.
Figure 3. Flow chart of the study.
Sensors 24 03325 g003
Figure 4. Graphical representation comparing COP-related parameters computed using EquiTest® (x-axis) and hunova® (y-axis) during static balance assessment. First raw: eyes open (EO); second raw: eyes closed (EC).
Figure 4. Graphical representation comparing COP-related parameters computed using EquiTest® (x-axis) and hunova® (y-axis) during static balance assessment. First raw: eyes open (EO); second raw: eyes closed (EC).
Sensors 24 03325 g004
Figure 5. Graphical representation comparing COP-related parameters computed with EquiTest® (x-axis) and hunova® (y-axis) during dynamic balance assessment. First raw: eyes open (EO); second raw: eyes closed (EC).
Figure 5. Graphical representation comparing COP-related parameters computed with EquiTest® (x-axis) and hunova® (y-axis) during dynamic balance assessment. First raw: eyes open (EO); second raw: eyes closed (EC).
Sensors 24 03325 g005
Table 1. Results of the Pearson’s ρ correlations between COP-related balance measures from EquiTest® and hunova® in EO and EC conditions during static tasks.
Table 1. Results of the Pearson’s ρ correlations between COP-related balance measures from EquiTest® and hunova® in EO and EC conditions during static tasks.
EquiTest® hunova®
MeanSTDMeanSTDPearsonp
EOSA (cm2)
APO range (cm)
MLO range (cm)
5.2911.6110.0712.390.5960.000
3.092.224.012.560.3550.013
1.731.633.042.140.5200.000
Path Length (cm)47.0221.0857.9635.230.4740.001
ML speed (cm/s)1.200.421.150.690.5100.000
AP speed (cm/s)1.740.931.541.030.4590.001
RMS (cm)0.710.510.970.590.4570.001
ECSA (cm2)
APO range (cm)
MLO range (cm)
16.1533.7132.3029.430.5720.000
5.153.387.093.730.5740.000
2.692.835.762.970.4510.001
Path Length (cm)76.3556.03127.8288.930.6860.000
ML speed (cm/s)1.600.892.251.310.5400.000
AP speed (cm/s)3.082.523.652.830.7220.000
RMS (cm)1.190.981.780.880.5530.000
Table 2. Results of the Pearson’s ρ correlations between COP-related balance measures from EquiTest® and hunova® in EO and EC conditions during dynamic tasks.
Table 2. Results of the Pearson’s ρ correlations between COP-related balance measures from EquiTest® and hunova® in EO and EC conditions during dynamic tasks.
EquiTest®hunova®
MeanSTDMeanSTDPearsonp
EOSA (cm2)
APO range (cm)
MLO range (cm)
16.5217.26112.59129.850.4980.000
8.344.7712.076.490.5060.000
3.073.139.727.110.3370.018
Path length (cm)106.7379.32164.67154.400.6530.000
ML speed (cm/s)1.891.222.222.180.5330.000
AP speed (cm/s)4.533.695.004.970.6220.000
RMS (cm)1.851.133.261.900.5610.000
ECSA (cm2)
APO range (cm)
MLO range (cm)
39.4338.21309.91229.960.4130.004
11.634.7219.807.560.4360.002
4.343.4015.437.680.3440.016
Path length (cm)146.3683.32257.18158.510.6210.000
ML speed (cm/s)2.491.543.952.610.4030.004
AP speed (cm/s)6.323.697.564.830.6680.000
RMS (cm)2.771.355.622.280.4350.002
Table 3. Results of the Pearson’s ρ correlations between global balance measures from EquiTest® and hunova® in EO and EC conditions during dynamic tasks.
Table 3. Results of the Pearson’s ρ correlations between global balance measures from EquiTest® and hunova® in EO and EC conditions during dynamic tasks.
EquiTest®hunova®
Mean STDMean STD Pearsonp
SOM4.4 9.75.8 6.30.7100.000
VIS10.5 15.620.3 27.00.5730.000
VEST21.7 22.084.8 110.50.4940.000
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

Podda, J.; Marchesi, G.; Bellosta, A.; Squeri, V.; De Luca, A.; Pedullà, L.; Tacchino, A.; Brichetto, G. Testing Dynamic Balance in People with Multiple Sclerosis: A Correlational Study between Standard Posturography and Robotic-Assistive Device. Sensors 2024, 24, 3325. https://doi.org/10.3390/s24113325

AMA Style

Podda J, Marchesi G, Bellosta A, Squeri V, De Luca A, Pedullà L, Tacchino A, Brichetto G. Testing Dynamic Balance in People with Multiple Sclerosis: A Correlational Study between Standard Posturography and Robotic-Assistive Device. Sensors. 2024; 24(11):3325. https://doi.org/10.3390/s24113325

Chicago/Turabian Style

Podda, Jessica, Giorgia Marchesi, Alice Bellosta, Valentina Squeri, Alice De Luca, Ludovico Pedullà, Andrea Tacchino, and Giampaolo Brichetto. 2024. "Testing Dynamic Balance in People with Multiple Sclerosis: A Correlational Study between Standard Posturography and Robotic-Assistive Device" Sensors 24, no. 11: 3325. https://doi.org/10.3390/s24113325

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