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Psychometric Characteristics of Smartphone-Based Gait Analysis in Chronic Health Conditions: A Systematic Review

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26 January 2025

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27 January 2025

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Abstract
Background/Objectives: Chronic health conditions frequently result in gait disturbances, impacting quality of life and mobility. Smartphone-based gait analysis has emerged as a promising alternative to traditional methods, offering accessibility, cost-effectiveness, and portability. This systematic review evaluates the validity, reliability, and sensitivity of smartphone-based inertial measurement units for assessing gait parameters in individuals with chronic conditions. Methods: A comprehensive literature search in Web of Science, PubMed, Google Scholar, and SportDiscus identified 54 eligible studies. Results: Validity was evaluated in 70% of the included studies, with results showing moderate-to-strong associations between smartphone apps and gold-standard systems (e.g., Xsens), particularly for parameters such as gait speed and stride length (e.g., r = 0.42–0.97). However, variability was evident across studies depending on the health condition, measurement protocols, and device placement. Reliability, examined in only 27% of the included studies, displayed a similar trend, with intraclass correlation coefficients (ICCs) ranging from moderate (ICC = 0.53) to excellent (ICC = 0.95) for spatiotemporal parameters. Sensitivity and specificity metrics were explored in 41% and 35% of the included studies, respectively, with several applications achieving over 90% accuracy in detecting gait abnormalities. Feasibility was rated positively in 94% of the included studies, emphasizing the practical advantages of smartphones in diverse settings. Conclusions: Overall, the findings of this systematic review underscore the clinical potential of smartphones for remote and real-world gait analysis, while highlighting the need for standardized methodologies. Future research should adopt a more comprehensive approach to psychometric evaluation, ensuring that reliability aspects are adequately explored. Additionally, long-term studies are needed to assess the effectiveness of smartphone-based technologies in supporting personalized treatment and proactive management of chronic conditions.
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1. Introduction

Chronic health conditions significantly contribute to reduced mobility and diminished quality of life worldwide, placing a considerable burden on healthcare systems (1, 2). These conditions, prevalent across all age groups, often manifest in gait disturbances, which not only impair daily functioning but also serve as key indicators of overall health and disease progression (3). Gait disorders are linked to adverse health outcomes, including falls, fractures, loss of independence, and mortality. (4–7). For example, studies have shown that slower gait speed is a predictor of frailty and higher mortality risk, while abnormalities in cadence and step length can indicate underlying neuromuscular or cardiovascular issues (6, 7). In this context, a systematic review and meta-analysis revealed that individuals with persistent low back pain exhibit a slower walking speed and a shorter stride length compared to healthy controls without back pain (8). Therefore, precise gait analysis is essential not only for understanding the severity and progression of chronic diseases but also for enabling early intervention to prevent falls and related complications.
Traditionally, gait assessment has relied on sophisticated and expensive technologies, including motion capture systems and force plates, typically available only in specialized clinical or research settings (9). Additionally, these systems require trained personnel and extensive infrastructure, limiting their accessibility and feasibility for widespread clinical use. Moreover, these methods are time-consuming and often impractical for monitoring patients in real-life or home-based environments (10, 11). As such, the need for alternative solutions has become increasingly evident, particularly during global health crises such as the COVID-19 pandemic, which underscored the importance of remote monitoring technologies.
Recent advances in mobile technology have highlighted smartphones as promising tools for gait analysis (12–14). With embedded sensors such as accelerometers and gyroscopes, smartphones offer a cost-effective, portable, and accessible solution for capturing motion data (15, 16). These devices enable both real-time and long-term monitoring of gait parameters in natural environments, providing insights that are often more representative of a patient’s functional abilities (17). Studies in populations such as individuals with Parkinson’s disease, Multiple Sclerosis and/or healthy older adults have demonstrated the utility of smartphone-based gait analysis (18–24).
Earlier systematic reviews have focused on specific populations, such as individuals with Parkinson’s disease or Multiple Sclerosis (25, 12). The results showed that smartphone applications have great potential to validly assess gait and balance impairments in individuals with Multiple Sclerosis and Parkinson's disease, but that further studies are needed to comprehensively evaluate their reliability and sensitivity (25, 12). However, to the best of the authors’ knowledge, no comprehensive review has yet synthesized the psychometric properties of smartphone-based gait analysis across a broad range of health conditions and age groups. Addressing this gap isessential, as it may offer valuable insights into the potential generalisability of smartphone-based gait analysis across a wide spectrum of health conditions and age groups. Therefore, this systematic review aims to critically evaluate the validity, reliability, and sensitivity of smartphone-based gait analysis in young and older adults with different chronic conditions. By synthesizing the existing evidence, this review seeks to assess the clinical potential of smartphone-based inertial measurement units (IMU) for gait monitoring, identify limitations in current research, and propose directions for future studies.

2. Methods

The present systematic review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (26). Additionally, this study has been registered on the Open Science Framework (OSF) at https://doi.org/10.17605/OSF.IO/QFU8D. Search strategy
A comprehensive literature search was conducted for studies published between 2014 and 2024, utilizing the electronic databases: Web of Science, PubMed, Google Scholar and SportDiscus. Only peer-reviewed studies written in English were included. The timeframe chosen reflects an important consideration: prior to 2014, the integration of smartphones and related technologies into daily life was less widespread, limiting their use in general and specifically in gait analysis. Keywords were collected through expert opinion, literature review, and controlled vocabulary (e.g., Medical Subject Headings [MeSH]). The search was carried out using the Boolean operators “AND” and “OR”. In the following our search strategy applied with PubMed: ("Gait" [MeSH] OR "Gait Analysis" OR "Walking" OR "Locomotion") AND ("Mobile Applications" OR "Smartphones" OR "Wearable Devices" OR "Mobile Health") AND ("Pathological Conditions, Anatomical" [MeSH] OR "Neurological Diseases" OR "Musculoskeletal Diseases" OR "Chronic Diseases" OR "Parkinson Disease" OR "Stroke" OR "Multiple Sclerosis" OR "Arthritis" OR "COPD" OR "low back pain"). Additional manual searches of reference lists were performed. Two review authors (TB and CF) conducted the study selection process independently, who screened the titles and abstracts of all identified records. Each author compiled a list of potentially eligible studies based on the inclusion criteria. These lists were then compared and discussed to reach a consensus. In cases of discrepancy, a third author (HC) was consulted to ensure an unbiased and rigorous selection process.

Inclusion and Exclusion Criteria

The inclusion criteria for eligible studies were elaborated based on the PICOS (Population, Intervention, Comparison, Outcome, Study Design) approach. The following criteria were defined: (1) Population: young and old adult participants (age ≥ 18 years) with chronic health conditions (e.g., Parkinson’s disease, Multiple Sclerosis, musculoskeletal, cardiovascular and metabolic diseases) (2) Intervention: smartphone-based gait analysis using embedded IMUs, (3) Comparison: gold-standard methods for gait analysis (e.g., motion capture systems, force plates) or other validated assessment tools (e.g., trundle wheel or XSens), (4) Outcome: validity, reliability, sensitivity, and feasibility data (5) Study design: observational studies, cross-sectional studies, cohort studies or validation studies.
Studies were excluded if they focused solely on healthy participants, involved individuals under 18 years of age, were not in English, and lacked assessments of reliability, validity, sensitivity, and feasibility. The focus on adults (age ≥ 18 years) was chosen to avoid variability arising from maturation changes in younger populations, which are better suited to separate investigations.

Data Extraction and Analysis

From the included studies, detailed data were extracted, including participant demographics such as sample size, age, sex, and underlying chronic conditions. Information about the study design and context, including whether the study was cross-sectional, observational, or a prospective cohort study, was also recorded. Data were systematically gathered on the devices and applications used, such as the smartphone models, application names, intended users, test location and sensor placement (e.g., sternum or pocket). Key gait parameters, including velocity, step length, and cadence, were noted alongside the gold-standard systems used for validation, such as motion analysis platforms or pressure-sensitive mats. The primary outcomes focused on test–retest reliability, typically reported as intraclass correlation coefficients (ICCs) or typical error of measurement (TEM), and validity metrics, often expressed through correlation or agreement with gold standards. Furthermore, sensitivity, specificity, feasibility, main findings, intended users, and limitations of the studies were extracted. The results of the included studies were qualitatively synthesized. Descriptive analyses were performed to compare reliability and validity outcomes across studies, while variations in device placement and methodologies were highlighted as potential sources of heterogeneity.

Methodological Quality Appraisal

The methodological quality of the included studies was assessed using a modified version of the "Quality Assessment Tool for Observational Cohort and Cross-Sectional Studies" originally developed by the National Institute of Health (27). This tool initially comprises 14 criteria, each rated as "Yes" or "No". The quality of the studies was classified using clearly defined thresholds: studies with a "Yes" response for at least 8 criteria were categorized as "good quality," those with 5 to 7 positive assessments were considered "fair quality," and studies with fewer than 5 positive ratings were classified as "low quality” (28).

3. Results

Study Selection

The study selection process and its outcomes are displayed in Figure 1. The search initially identified a total of 946 studies. After removing duplicates, 867 unique studies remained for further evaluation. Screening the titles and abstracts led to the exclusion of 746 studies. Consequently, the full texts of the remaining 121 studies were reviewed. Of these, 45 studies were excluded for not assessing the reliability or validity of gait measurements, 15 studies were excluded due to their focus on healthy participants, and 7 studies were excluded because they involved participants younger than 18 years. Finally, our systematic literature search resulted in 54 studies eligible for inclusion.

Study Analysis

The results from a total of 54 studies investigating smartphone-based applications for gait analysis are displayed in Table 1. The number of participants varied significantly across studies, ranging from 10 (29) to 1414 participants (30). Overall, 70% (38 studies) of the included studies focused on participants with specific health conditions such as Parkinson's disease (31) or Multiple Sclerosis (32). The remaining 30% (16 studies) analysed either neurological conditions (33) or patients with other conditions like rheumatoid arthritis (34). The average age of participants ranged from 21 years (35) to 73 years (36). Around 29 studies (54%) focused on middle-aged adults (40 to 65 years). Of the 54 studies, 15 studies (28%) were cross-sectional, 11 studies (20%) observational, five (9%) prospective, four validation (7%) studies while 6% (3 studies) used longitudinal designs.
Additionally, 52% (28 studies) (37–43, 31, 44–57, 35, 36, 58–61) of the included studies conducted measurements in clinical settings, 37% (20 studies) (37, 62, 38, 63, 29, 64, 40, 65–69, 20, 70, 71, 30, 53, 72–74) collected data in home environments, and 7% (4 studies) (38–40, 53) combined both clinical and home settings. Parkinson's disease was the most commonly studied health condition, with 46% (25 studies) (62, 37, 63, 29, 41, 65, 31, 45, 68, 75, 20, 69, 70, 48, 71, 30, 53, 52, 76, 72, 56, 77, 36, 60, 61), Multiple Sclerosis was investigated in 10 studies (19%) (38, 39, 64, 32, 66, 67, 78, 55, 73, 74), stroke was the focus of three studies (6%) (44, 46, 54), rheumatoid arthritis was addressed in two studies (4%) (34, 59), as well as pulmonary diseases (4%) (47, 79) and only one study focused on chronic low back pain patients (2%) (80).
The range of smartphone models used in the studies was diverse. 14 studies (26%) employed iPhone models, including older devices like the iPhone 4s (40) and newer models like the iPhone 13 (58). Eight studies (15%) used specialized apps like the mPower app (37, 71), while 16 studies (30%) relied on standard apps such as Google Fit or proprietary applications, as seen in the work from Polese et al. (54). Of the 54 studies, 32 (62%) placed the smartphone at the hip or in the pocket, such as in the works by Adams et al. (37) and Balto et al. (39). Six studies (11%), including e.g., Regev et al. (55), positioned the devices on the chest, while fewer than 5% of included studies (2 studies) examined alternative positions, such as the thigh (43) or the sacrum (41).
Gait speed was measured in 47 studies (87%), including works by Tang et al. (36) and Adams et al. (37). Step length and stride length were a focus in 32 studies (59%), such as Capecci et al. (41) and Mehrang et al. (71). Gait variability and fluctuation width were analysed in 16 studies (30%), including Kim et al. (20) and Pepa et al. (53). Five studies (9%), such as Kim et al. (20), investigated specific parameters like the freezing index. Validation was addressed in 17% of the included studies (9 studies). To validate smartphone measurements, 19 studies (35%) used biomechanical analysis methods such as video analysis (e.g., (41)). Clinical scales like the Expanded Disability Status Scale were used in 20% of the studies (11 studies), like Creagh et al. (66). Wearable sensors such as actigraphs were employed in 24% of the studies (13 studies), as in the work by Brooks et al. (40).

Validation, Reliability and Feasibility Outcomes

Table 2 summarizes the psychometric properties of smartphone-based gait analysis across various pathological conditions. Among the 54 studies included in this review, 70% (38 studies) investigated the validity of smartphone-based gait analysis. These studies primarily evaluated concurrent validity by comparing smartphone-derived metrics with gold standard systems such as video analysis, standalone accelerometers, or force plates. Correlation coefficients (r) ranged from 0.42 to 0.97, highlighting variability in the strength of agreement across different conditions, populations, and measurement protocols. ICC values for agreement varied from 0.53 to 0.96. Additional validity aspects, including criterion (assessed in 28 studies, 52%) and construct validity (assessed in 6 studies, 11%), were investigated in a total of 34 studies (63%). These studies utilized metrics such as sensitivity (ranging from 43% to 98%) and specificity (ranging from 59% to 97%), primarily derived through ROC analyses to evaluate diagnostic accuracy.
Reliability was explored in 27% of studies (15 studies), focusing on test-retest reliability and, less commonly, inter- and intra-rater reliability. ICC values reported for temporal and spatiotemporal gait parameters ranged from 0.53 to 0.95, and the standard error of measurement (SEM) was documented in two studies (4%). Sensitivity and specificity were addressed in 41% (22 studies) and 35% (19 studies) of the included studies, respectively. The reported sensitivity and specificity for distinguishing pathological gait patterns from healthy controls ranged broadly, with values frequently exceeding 90% for detecting conditions such as Parkinson's disease and Freezing of Gait (FoG). However, 11 studies (20%) reported moderate accuracy, emphasizing the need for standardized methodologies and more robust algorithms. Feasibility was positively rated in 94% of the included studies (51 studies). Practical limitations such as sensor placement inconsistencies and environmental interferences (e.g., ambient noise) were noted in 12 studies (22%).

Methodological Quality of the Included Studies

The methodological quality of the included studies is summarized in Table 3. 87% of the studies (47 studies) met requirements such as clear definitions of the target population and adequate sample sizes. However, notable weaknesses were observed in the blinding of assessors and the use of standardized measurement protocols. Only a small proportion of the studies (approximately 20%) reported fully blinded outcome assessments. Statistical analyses, however, were generally considered appropriate and robust, with a variety of approaches used, including linear models (e.g., regressions or ANOVAs), ICC calculations, and ROC analysis. Consequently, the majority (96%) of the included studies (52 studies) were rated as having a “good overall methodological quality” with two studies only rated as having a “fair overall quality”.

4. Discussion

The objective of this study was to critically appraise the psychometric properties of smartphone-based gait analyses across various chronic diseases. Overall, the findings indicate that smartphone applications represent a valid, cost-effective, and accessible alternative to traditional gait analysis methods, such as motion capture systems or force plates, for assessing gait parameters across different chronic diseases, both in clinical and home environments. Additionally, the reliability of smartphone-based gait analysis can generally be rated as good, emphasizing the potential of smartphone applications to deliver consistent results. However, it is important to note that reliability has been studied less extensively than validity. Sensitivity and specificity were investigated in 37% of the included studies, with the majority demonstrating high accuracy in distinguishing pathological from healthy gait patterns. Feasibility was confirmed in 94% of the studies, underscoring the widespread acceptance and practicality of these technologies across diverse settings.
The use of smartphone applications has gained remarkable attention over the last couple of years. This is because these devices offer a unique combination of portability, cost-efficiency, and accessibility, making them suitable for both clinical assessments and home-based monitoring. Their widespread adoption has been driven by advancements in sensor technology, allowing precise and comprehensive data collection directly from everyday devices. Furthermore, the integration of machine learning algorithms has enhanced their ability to process and analyze gait-related data with high accuracy, further cementing their utility in modern healthcare practices. Among the included studies, 70% evaluated validity by comparing results with clinical or biomechanical reference systems. Brooks et al. (40) examined the concurrent validity and demonstrated a high correlation between app-based and clinical walking distance measurements (r = 0.89) in patients with congestive heart failure and pulmonary hypertension aged between 25 and 76 years. Likewise, Polese et al. (54) reported excellent agreement between Google Fit and actual step counts measured with video analyses (ICC = 0.93) in stroke survivors patients aged 62 years. Furthermore, Tang et al. (36) reported strong correlations between a smartphone and the XSens system in Freezing of Gait (FoG) detection (r = 0.86 to 0.97) in Parkinson patients aged 73 years, reflecting a good concurrent validity. Moreover, Chen et al. (65) reported using a self-designed framework for mobile phones a sensitivity of 97.3% and a specificity of 97.1% in classifying Parkinson’s severity based on gait variability. Such results underscore the excellent discriminative validity and the potential of smartphone-based apps to replace traditional gait analysis systems, particularly in resource-limited settings where access to expensive technologies like force plates or motion capture systems is restricted. Despite these positive findings, some studies highlighted some limitations. For instance, Balto et al. (39) conducted a study including patients with Multiple Sclerosis (46 ± 10 years) and found that certain apps, such as Health, Health Mate and Moves, did not exhibit significant correlations with walking speed. This highlights the importance of carefully selecting appropriate algorithms, applications, and devices. It is indeed evident that not all smartphones and apps are equally suitable (39), which can significantly influence validity and reliability outcomes. These findings highlight the versatility of specific smartphone applications in capturing gait-related parameters.
Reliability was investigated in only 27% of the included studies, with consistently positive results. This indicates that, despite its relevance, reliability was relatively neglected. Bourke et al. (64) reported ICC values ranging from 0.53 to 0.96 for spatiotemporal parameters measured with the FLOODLIGHT software on the smartphone. Creagh et al. (67) demonstrated for patients with Multiple Sclerosis aged 40 years excellent reliability of step counts with an ICC of 0.91. Similar results were reported by Serra-Ano et al. (56), who found ICC values ranging from 0.89 to 0.92 for gait analyses using the FallSkip® app in patients with Parkinson disease aged 69 years. In the same sense, Tang et al. (36) reported high reliability in FoG detection (ICC = 0.768–0.896) for persons aged 73 ± 9 years. Overall, there is evidence that smartphone-based gait analyses provide consistent results, even though data in some areas, such as inter-rater reliability (2 of 54 studies [4%]), remain limited and methodological standardization is still lacking. However, the question remains as to why so few studies have investigated reliability. This could suggest that many apps and devices are designed primarily for single measurements and have not been adequately validated for long-term use or in varying contexts. Future research should focus more on inter- and intra-rater reliability, particularly for applications intended for clinical practice or remote monitoring.
The ability of smartphones to differentiate pathological from healthy populations was examined in 37% of the included studies (20 studies). For example, Arora et al. (29) revealed sensitivity and specificity values of over 90% in distinguishing Parkinsons patients from controls. Similar findings have been reported by Tang et al. (36). Likewise, Mehrang et al. (71) and Pepa et al. (53) demonstrated moderate-to-high accuracy of smartphone algorithms in identifying Parkinson’s disease based on gait parameters, with sensitivity reaching up to 84.9% and specificity up to 95.2%. Additionally, Creagh et al. (67) demonstrated that smartphone-based models could classify gait abnormalities in patients with mild to moderate Multiple Sclerosis with high precision (88%). Such findings are particularly promising for the early detection of gait disorders in the general population. However, results varied depending on the target population and algorithms used, as illustrated by Polese et al. (54), who reported excellent agreement between the actual step count counted with video analysis and the step count from the mobile phone in stroke survivors (ICC = 0.93), in contrast to Balto et al. (39), where certain applications failed to correlate with walking speed in Multiple Sclerosis patients. This emphasizes the importance of tailoring algorithms to specific diseases and populations.
The feasibility of smartphone-based gait analyses was addressed in almost all studies (51 of 54 (94%)), with the majority highlighting their ease of use at home and in clinical settings. Of note, device placement varied considerably across the included studies, from pockets to the hip or chest. While Kim et al. (20) found that the position of the smartphone did not significantly affect FoG detection, Creagh et al. (67) and Brinkløv et al. (81) stressed that inconsistent placements could lead to significant measurement errors. Additionally, Brinkløv et al. (81) showed that placing smartphones in jackets caused higher measurement errors. This highlights the need for standardized methods. Additionally, Abujrida et al. (62) reported that noise disturbances in home environments could affect data quality. Nonetheless, there is evidence indicating high participant acceptance and satisfaction with smartphone use in home settings (70). Such positive feedback is crucial for promoting acceptance of these technologies, especially in remote monitoring. However, only 19% of the included studies examined the feasibility and acceptance of the technologies. This is a critical aspect, as patients with motor impairments such as tremor or rigidity might face challenges in using such tools. Future studies should prioritize addressing the specific needs of the target population to ensure that these technologies are both accessible and practical for all user groups. Additionally, the role of smartphones in long-term monitoring and personalized treatment remains a promising but underexplored topic.

5. Limitations and Future Research Perspectives

Certain limitations of smartphone-based gait analysis are evident and warrant further investigation. While validity was the primary psychometric feature investigated—reported in 70% of the included studies—reliability received comparatively little attention, with only 27% of studies addressing it. Among these, inter-rater reliability was particularly underrepresented, investigated in just 4% of the studies. This imbalance suggests a need for future research to adopt a more comprehensive approach to psychometric evaluation, ensuring that reliability aspects are adequately explored. In addition, a key challenge lies in the lack of standardization across studies, particularly regarding device placement, algorithm design, and measurement protocols. Inconsistent methodologies can significantly influence the validity and reliability of findings, limiting their generalizability. Additionally, user experience and satisfaction with smartphone technologies remain underexplored, especially in populations with significant mobility challenges, such as those with advanced motor impairments. Future research should address these gaps by prioritizing the development of standardized methodologies and refining algorithms tailored to specific diseases and populations. Furthermore, feasibility studies should focus on the needs of diverse user groups to ensure accessibility and practicality in both clinical and home environments. Long-term investigations into the effectiveness of smartphone-based technologies are also needed to evaluate their potential for personalized treatment and proactive management of chronic conditions. These advancements could promote the widespread adoption of smartphone-based gait analysis tools and enhance their impact on healthcare delivery.

6. Conclusions

This review underscores the growing role of smartphone applications in assessing gait parameters across various chronic conditions. Overall, the summarised evidence supports their capability to deliver valid, reliable, and sensitive measurements of gait impairments, as well as their utility in distinguishing pathological gait patterns from those of healthy individuals. These findings emphasize the potential of smartphone-based gait analysis to contribute meaningfully to clinical practice and remote monitoring. Smartphone applications have the potential to transform gait analysis by providing accessible, cost-effective, and scalable solutions for monitoring patients in their natural environments.

Author Contributions

Conceptualization, T.B. and H.C.; methodology, T.B., H.C. and C.F.; validation, T.B. and C.F.; investigation, T.B.; writing—original draft preparation, T.B.; writing—review and editing, H.C. and L.S.; All authors have read and agreed to the published version of the manuscript.

Funding

This research received no funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

None.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Flowchart for the inclusion and exclusion process for all studies of the systematic review.
Figure 1. Flowchart for the inclusion and exclusion process for all studies of the systematic review.
Preprints 147366 g001
Table 1. Characteristics of the included studies.
Table 1. Characteristics of the included studies.
Reference Participants Study design Intended users / Test location Disease Mobilephone (App) Placement Gait parameters Reference (system)
n Sex Age
Abujrida et al., (62) 152 m(-)/f(-) - Cross-sectional study PD-patients / at home Parkinson IPhone (mPower) Pocket Sway area, gait velocity, cadence, step time, step length, step count -
Adams et al., (37) 82 m(46)/f(36) 63.3 ± 9.4 Observational study Parkinson and HC / in clinic & at home Parkinson Iphone 10 and Iphone 11 (BrainBaseline™ App) Hip Gait speed, step length, stride length
Alexander et al., (38) 100 m(30)/f(70) Median: 53.5 (IQR: 47.8 - 58.0) Pilot-/Validationstudy MS-patients / Clinical (Indoor) & Home (Outdoor) Multiple Sclerosis Iphone 6s (mSteps App) Arm Distance walked Trundle wheel
Arora et al., (29) 10 m(7)/f(3) 65.1 ± 9.80 Prospektive cohort study PD-patients / at home Parkinson LG Optimus S (Specialized Software) Hip - Modified UPDRS
Arora et al., (63) 334 m(210)/f(124) 66.1 ± 9.0 Prospektive cohort study PD-patients / at home Parkinson LG Optimus S (-) - - Modified UPDRS
Balto et al., (39) 45 m(-)/f(-) 46.7 ± 10.0 Cross-sectional study MS-patients / laboratory Multiple Sclerosis Iphone 5 / Health (Apple), Health Mate (Withings), and Moves (ProtoGeo Oy) Pocket Acceleration, velocity Digi-Walker SW-200 pedometer (Yamax), UP2 and UP Move (Jawbone),
Flex and One (Fitbit)
Banky et al., (33) 35 m(22)/f(13) 51.2 (19-85) Observational, criterion-standard comparison study Neurological patients / rehabilitation center Neurological conditions Samsung Galaxy S5 (-) - Joint angular velocity Optitrack 3-D motion analysis
Bourke et al., (64) 51 m(24)/f(27) 39.5 ± 7.9 Cross-sectional study MS-patients / at home Multiple Sclerosis Samsung Galaxy S7 (FLOODLIGHT) Waist in belt bag or pocket Spatiotemporal parameters -
Brinkløv et al., (81) 27 m(9)/f(18) 64.2 ± 5.9 Validation Study Type 2 diabetes patients / field Type 2 diabetes Iphone 5c (InterWalk) Pocket VO2peak estimation, acceleration vector magnitude Cosmed K4b2
Brooks et al., (40) 38 m(11)/f(27) 25 - 76 Validation study CHF- and pHTN-patients / clinic and home CHF and pHTN Iphone 4s (SA-6MWT App) Pocket or Hip holster Walking distance, step count ActiGraph accelerometer
Capecci et al., (41) 20 m(15)/f(5) 67.6 ± 9.1 Controlled Cross-sectional study PD-patients / in clinic Parkinson Iphone 5 (Specialized Software) Hip joint Cadence, freezing index, energy index Videoanalyse
Chan et al., (80) 20 m(11)/f(9) 20 - 65 Observational study Chronic Low back Pain patients / in clinic LBP Iphone 4 (-) Lower back Cadence, step length, velocity, stride time Minimod
Chen et al., (65) 37 m(-)/f(-) - Prospektive cohort study PD-patients / at home Parkinson LG Optimus S (-) Pocket Gait variability MDS-UPDRS
Cheng et al., (32) 76 m(36)/f(40) 39.5 ± 7.9 Cross-sectional study Clinicans and MS-patients Multiple Sclerosis Samsung Galaxy S7 Waist or pocket Timed 25 Foot Walk Stopwatch in clinical setting
Chien et al., (43) 20 m(2)/f(19) 67.95 ± 7.30 Observational study Patients with orthostatic tremor / in clinic Orthostatic tremor iPhone 6s (custom app) Sacrum Mean frequency of acceleration, walking speed -
Clavijo-Buendía et al., (31) 30 m(15)/f(15) 71.7 ± 5.1 Observational study PD-patients / in clinic Parkinson Samsung Galaxy S8 (RUNZI ®App) Front Thigh Cadence, step length, step count, gait velocity -
Costa et al., (44) 55 m(30)/f(25) 62.5 ± 14.9 Observational study Stroke survivors / laboratory Stroke Iphone 6s and S480 Positivo (Google Fit, STEPZ, Pacer) Paretic/non-paretic hip pocket Step count Actual steps (live and video analysis)
Creagh et al., (67) 73 m(23)/f(50) Mild 39.3 ± 8.3 / moderate 40.5 ± 6.9 Observational study MS-patients / at home Multiple Sclerosis Samsung Galaxy S7 (-) Anterior waist Step count -
Creagh et al., (66) 52 mild MS; 21 moderate MS m(16)/f(36); m(7)/f(14) 39.3 ± 8.3; 40.4 ± 6.9 Longitudinal study MS-patients / at home Multiple Sclerosis Samsung Galaxy S7 (Floodlight PoC App) Pocket or Belt Bag Only adherence of 2MWT over study duration Expanded Disability Status Scale (EDSS)
Ellis et al., (45) 12 m(7)/f(5) 65.0 ± 8.4 Validity study PD-patients / in clinic Parkinson Apple iPod Touch (SmartMOVE) Torso (Navel) Step time, step length Pressure sensor mat (Steplength)
Footswitch (Steptime)
Ginis et al., (68) 40 m(23)/f(17) 68.6 ± 6.8 Pilot RCT PD-patientes / at home Parkinson Samsung Galaxy S3 Mini (ABF-gait app and CuPiD) Pocket (training) and
handheld (FOG training)
Gait speed, stride length, double support time (single and dual task) PKMAS instrumented walkway
Goñi et al., (75) 610 m(399)/f(211) 60.3 ± 8.94 Cross-sectional study PD-patients and HC / remote, self-administered Parkinson x/(mPower app) - Average acceleration, number of steps, stride intervall,
stride variability
-
Hamy et al., (34) 399 m(-)/f(-) - Observational study RA-patients / remote Rheumatoid arthritis Iphone (PARADE App) Pocket Step length, step time GAITRite mat
He et al., (69) 119 m(72)/f(47) 64.1 ± 7.9 Observational study Parkinsonpatients / at home Parkinson Iphone 4s and newer (NeuroEnhanceNet) Pocket - -
Isho et al., (46) 24 m(12)/f(12) 71.6 ± 9.7 Cross-sectional study Older adults / in clinic Chronic Stroke Sony Xperia Ray SO-03C (-) L3 Trunk acceleration while gait
(anteropsoterior, mediolateral)
interstride variability
-
Juen et al., (47) 28 m(12)/f(16) 50 - 89 Cross-sectional study Stroke survivors / laboratory Pulmonary diseases Samsung Galaxy S5, Ace (MoveSense) L3 Walking distance, walking speed (6MWT), step count Actigraph GT3X
Kim et al., (20) 15 m(7)/f(8) - Cross-sectional study PD-patients / at home Parkinson Google Nexus 5 (-) Waist, pocket, ankle, chest Freezing index, acceleration signals Videoanalyse
Lam et al., (78) 94 m(26)/f(68) 46.5 ± 10.6 Longitudinal study MS-patients and Healthy / remote Multiple Sclerosis x/(MS Sherpa App) - Walking distance EDSS, T25FW
Lipsmeier et al., (70) 43 m(35)/f(8) 57.5 ± 8.45 Prospektive cohort study PD-patients / at home Parkinson Samsung Galaxy S3 Mini (Roche PD Mobile App v1) Pocket or belt pouch Turn speed, activity ratio, sit-to-stand transitions MDS-UPDRS
Lopez et al., (48) 10 m(7)/f(3) 45 - 65 Cross-sectional study PD-patientes / gait lab (MOVISYS) Parkinson x/(Listenmee app) - Walking speed, stride length, cadence,
freezing of gait
Vicon Motion System
Mak et al., (49) 110 m(109)/f(1) 68.9 ± 5.9 Observational study Cardiovascular patients, remote and clinical Cardiovascular disease Iphone 7 (VascTrac App) Pocket Step count Clinical Measure "Ground Truth"
Maldaner et al., (50) 70 m(43)/f(27) 55.9 ± 15.4 Observational study Lumbar degenerative disc patients / in clinic Lumbar degenerative disc disease (6WT App) - Walking distance 6 min walk normdata and Distance Wheel
Marom et al., (51) 28 m(17)/f(11) 42.5 ± 15.0 Cross-sectional study Rehabilitation patients / in clinic Unilateral lower limb disability Xiaomi Redmi Note 8 (OneStep App) Pockets (front) Cadence, gait speed, stride length, double support,
step length, swing/stance phase
C-Mill VR+ treadmill (Motek)
Mehrang et al., (71) 616 m(413)/f(203) 60.6 ± 10.1 Cross-sectional study PD-patients and HC / at home Parkinson Iphone 4s or newer (mPower App) Pocket or bag Cadence, step length -
Omberg et al., (30) 1414 m(481)/f(933) 60 Observational study - remote cohort study PD-patients/ at home Parkinson x/(mPower) pocket Average acceleration, jerk Clinical measures (ObjectivePD substudy)
Pepa et al., (52) 18 m(13)/f(5) 69.0 ± 9.7 Cross-sectional study PD-patients / in clinic Parkinson Samsung Galaxy (-) Pocket Step length, step cadence Videoanalyse
Pepa et al., (53) 44 m(-)/f(-) 68.02 ± 8.3 Cross-sectional study PD-patients / in clinic and a home Parkinson Iphone 5, Iphone 6s (-) Hip Step length, step cadence, freezing index, power index,
energy derivative ratio
Videoanalyse
Polese et al., (54) 37 m(28)/f(9) 62 ± 11 Observational study Strokepatients / in clinic Stroke LG Nexus 5 (Google Fit App) Paretic lower limb pocket Step count, walked distance Actual step count by examiner in videotape
Raknim et al., (76) 17 m(7)/f(10) 72.0 ± 6.8 Longitudinal study Older adults without neurological diseases Parkinson Android Smartphones Google, HTC, Samsung (-) Pocket Cadence, step length -
Regev et al., (55) 100 m(33)/f(67) 40.8 ± 12.4 Cross-sectional study MSpatients / in clinic Multiple Sclerosis x/(Mon4t Clinic™ app) Sternum 3m/10m TUG time, tandem walk metrics EDSS, clinical rater
Rozanski et al., (82) 25 m(12)/f(13) 63.9 ± 8.4 Retrospective repeated measures Patients in rehabilitation program / - Neurological or musculoskeletal conditions x/(OneStep) Left/right front or back pocket Cadence, velocity, hip range, base width, step
and stride lengths, stance and double support times,
asymmetries of stance, step length and double support
-
Salvi et al., (79) 30 m(11)/f(19) 50 ± 16.6 Longitudinal study PAH-patients / indoor and outdoor PAH Android or iPhone (SMWTApp) - Walking distance (6MWT) Observational by physiologists
Schwab et al., (72) 14 m(-)/f(-) - Observational study - remote cohort study PD-patients / remote at home Parkinson x/(mPowerApp) Pocket Tremor, rigidity, freezing of gait, linear and
angular acceleration
-
Serra-Ano et al., (56) 29 m(-)/f(-) 68.9 ± 8.98 Cross-sectional study PD-patients / in clinic Parkinson Xiaomi Redmi 4x (FallSkip®) Waist - Videoanalyse
Shema-Shiratzky et al., (57) 72 m(35)/f(37) 57.2 ± 1.9 Cross-sectional study Patients with muscosceletal pathology / in clinic Muscosceletal pathology (Knee, Back, Hip, Ankle) Samsung Galaxy A51 (OneStep App) Thigh Gait speed, cadence, steplength, cycle time,
single- und double-limb support, stancephase
The ProtoKinetics Zeno™ Walkway
Su et al., (77) 52 m(33)/f(19) 63 ± 10 Cross-sectional study PD-patients / in clinic Parkinson iPhone (-) Front pocket Stride time, stride time variability Mobility lab system
Sugimoto et al., (35) 22 m(8)/f(14) 21.5 ± 2.56 Cross-sectional study Recurrent Ankle Sprains patients / biomechanics lab Recurrent Ankle Sprains Samsung Galaxy Xcover 2 Model GTS7710L (AccWalker) Thigh Sagittal-plane thigh angular RoM 3D motion capture (Qualisys)
Tang et al., (36) 20 m(11)/f(9) 73.6 ± 9.1 Observational study PD-patients / in clinic Parkinson Sony Xperia XZ F8331 (-) L2 Stride time, step time, stance time, swing time,
step length, step velocity, freezing of gait
Xsens MTw Awinda
Tao et al., (58) 35 m(23)/f(12) 71.133 ± 8.585 Cross-sectional study HC and CSVD patients / laboratory Cerebral small vessel disease Iphone 13 (MobileGait app) Shank, waist Cadence, stride time, stance phase, swing phase,
stance time, stride length, walking speed
Inertial Measurement Unit (N200, Wheeltec, China)
Van Oirschot et al., (73) 25 m(15)/f(10) 40.0 ± 8.0 Cross-sectional study MS-patients / at home (outdoor) Multiple Sclerosis Android/iOS (MS Sherpa App) Pocket 2 MW distance, walking speed Distance markers
Wagner et al., (59) 30 m(8)/f(22) 61 (50 - 74) Validation Study RA-patients / laboratory Rheumatoid arthritis Google Pixel 4, Samsung Galaxy A02 (BeSafe-App) Waist pouch at right front hip Step count, walking speed, cadence Manual step count (100 Steps)
Yahalom et al., (60) 18 m(10)/f(8) 50.7 ± 8.8 Cross-sectional study PD-patients / in clinic Parkinson Iphone 6 (EncephaLog) Sternum Step length, cadence, mediolateral sway Videoanalyse
Yahalom et al., (61) 21 with normal pull test, 23
with unnormal pull test
m(11)/f(10); m(13)/f(10) 67.3 ± 6.8 / 67.8 ± 6.9 Cross-sectional study PD-patients / in clinic Parkinson IPhone (-) Waist Stride length, cadence, variability -
Zhai et al., (74) 67 m(25)/f(42) 42.9 ± 10.9 Cross-sectional study MS-patients / at home Multiple Sclerosis Samsung Galaxy S4 mini (-) - Mean vector magnitude, variance of vector magnitude steps/min ActiGraph
Abbreviations: CHF = Congestive heart failure, CSVD: Cerebral small vessel disease, EDSS: expanded disability status scale, f: female, HC: healthy controls, m: male, MDS – UPDRS: Modified unified Parkinson´s disease rating scale, MS: Multiple Sclerosis, PAH: Pulmonary arterial hypertension, PD: Parkinson Diseases, pHTN: Pulmonary hypertension, RA: Rheumatoid arthritis, RoM: Range of Motion, TUG: Timed up and go test, T25FW: Timed 25-foot walk, UPDRS: Unified Parkinson´s disease rating scale, 2MWT: 2 minute walk test, 6MWT: 6 minute walk test.
Table 2. Psychometric characteristics of the smartphone-based gait analysis across the different pathological diseases.
Table 2. Psychometric characteristics of the smartphone-based gait analysis across the different pathological diseases.
Reference Reliability Validity Sensitivity Specificity Feasibility and Limitations Main Results
Abujrida et al., (62) NP NP 96.0% for FoG detection
98.0% for FoG detection Yes, but noise in home environment affects data Machine learning accurately classified PD gait impairments, achieving high accuracy (up to 98%) and AUC values (up to 0.99)
Adams et al., (37) Test –retest
(ICC > 0.7)
Inter/intra-rater reliability NP
NP NP NP Yes Significant decrease in gait parameters over 12 months
Alexander et al., (38) NP Yes
Content
Criterion (concurrent)
(95% LOA with-in ± 5 m)
NP NP Yes, but GPS accuracy and signal only outdoor Outdoor GPS from mSteps showed acceptable agreement with the trundle wheel for the MS cohort. Indoor measurements showed high variability.
Arora et al., (29) NP NP 96.2% for PD discrimination 96.9% for PD discrimination Yes Demonstrated excellent discrimination between PD and HC using gait metrics.
Arora et al., (63) NP NP 91.9% for PD vs control 90.1% for PD vs control Yes Smartphones distinguished PD and controls with high accuracy; gait and balance were effective markers.
Balto et al., (39) NP No significant correlation was found
between smartphone applications
(Health, Health Mate, Moves) and
walking speed (p > 0.05) (12)
NP NP Yes Smartphone applications lacked the required accuracy and precision for step measurement, making them unsuitable for use in clinical research settings. (12)
Banky et al., (33) Test-retest
(ICC Absolute = 0.21 - 0.93;
ICC Relative: 0.40 - 0.99)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(Spearman r ≥ 0.80 for 74.8% of parameters)
NP NP Yes, but limited with knee data Smartphone application showed excellent validity (ICC > 0.8) for velocity, but poor accuracy for the knee.
Bourke et al., (64) Test-retest
(ICC = 0.68 - 0.95 for temporal gait parameters;
ICC = 0.53 - 0.96 for spatiotemporal, spatial gait parameters)
Inter/intra-rater reliability NP
NP NP NP Yes A single smartphone offers precise and reliable measurements of specific spatial, temporal, and spatiotemporal parameters during a self-administered 2-Minute Walk Test (2MWT). (12)
Brinkløv et al., (81) Test-retest
(ICC = 0.85 - 0.86)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(r2 = 0.45 - 0.60)
98% 77% Yes, but smartphone placement affects validity;
jackets induce higher measurement error
High reliability and validity for VO2-peak prediction with placement in pants. Sensitivity higher than specificity for risk stratification.
Brooks et al., (40) Test-retest
(r = 0.94)
Inter/intra-rater reliability
NP
Yes
Content
Criterion (concurrent)
(r = 0.89; CI = 0.78–0.99)
94% NP Yes, but limited to iOS devices High correlation between app-estimated and in-clinic measured distances (ICC = 0.85 – 0.89). Repeatable at-home results (CoV = 4.6%).
Capecci et al., (41) Test-retest NP
Inter/intra-rater reliability (ICC > 0.80)
NP 70.1% (Algorithmus 1)
87.57% (Algorithmus 2)
84.1% (Algorithm 1)
94.97% (Algorithm 2)
Yes, but only in a clinical setting Algorithm 2 showed significantly higher sensitivity and specificity than Algorithm 1
Chan et al., (80) Test-retest
(ICC > 0.4)
Inter/intra-rater reliability NP
NP NP NP Yes The results showed smart phones are feasible for gait tele-monitoring, with potential as prognostic and treatment outcome tools.
Chen et al., (65) Test-retest NP
Inter/intra-rater reliability
NP
Yes
Content
Criterion (concurrent)
(r = 0.54. p < 0.001 for PD severity assessment vs MDS-UPDRS)
97.3% for PD severity discrimination 97.1% for PD severity discrimination Yes, but requires consistent training and device management The framework achieved high accuracy and robustness in PD/HC classification and severity estimation
Cheng et al., (32) Test-retest
ICC = 0.87 (0.8 - 0.92)
Inter/intra-rater reliability NP
Yes
Correlation between turn speed at 5UTT and T25FW
(r=0.5, p < 0.001)
NP NP Yes A smartphone-based sensor measure for turn speed shows consistent reliability and concurrent validity in evaluating gait and balance impairments in people with Multiple Sclerosis
Chien et al., (43) Test-retest NP
Inter/intra-rater reliability
(ICC = 0.84–0.92 for mean frequency of acceleration measures (intra-group))
NP NP NP Yes, but limited sample size Significant mean frequency of acceleration differences between OT patients and controls indicate balance and gait instability in OT.
Clavijo-Buendía et al., (31) Test –retest
(ICC = good - excellent)
Inter/intra-rater reliability NP
Yes
Construct
(convergent)
(r = 0.424 - 0.957)
NP NP Yes Moderate to excellent correlation with 10-MWT, good to excellent test-retest reliability for RUNZI® parameters
Costa et al., (44) Test-retest
(ICC = 0.99 for actual steps;
ICC = 0.80 for Pacer iPhone;
ICC = 0.68 for Pacer Android;
ICC = 0.28 for STEPZ iPhone;
ICC = 0.20 for STEPZ Android;
ICC = -0.70 for Health iPhone;
ICC = 0.10 for Health Android)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(r = 0.18 for Health Iphone, p = 0.21)
(r = 0.80 for Pacer Iphone, p < 0.01)
(r = 0.65 for STEPZ Iphone, p < 0.01)
(r = 0.19 for Health Android, p = 0.19)
(r = 0.30 for STEPZ Android, p < 0.05)
(r = 0.68 for Pacer Android, p < 0.01)
NP NP Yes Pacer (iPhone) showed the highest validity (r = 0.80, p < 0.01) and reliability (ICC = 0.80).
Creagh et al., (67) Test-retest
(ICC = 0.91 for Step number;
r = 0.47 - 0.52 for T25FW p < 0.01)
Inter/intra-rater reliability NP
NP 67.5 % for mild MS
80.1 % for moderat MS
75.7 for mild vs moderat MS
60.3 % for mild MS
87.2 % for moderat MS
87.8 for mild vs moderat MS
Yes, but inconsistent device placement significantly impacts measurement accuracy
Models utilizing smartphone features demonstrated superior classification performance, enabling accurate and remote measurements with a single device. These models effectively distinguish gait-related dysfunction in individuals with moderate Multiple Sclerosis from healthy controls and those with mild MS. (12)
Creagh et al., (66) NP Yes
Content
Criterion (concurrent)
(95% LOA with-in ± 5 m)
NP NP Yes, but e.g., hall length influenced performance Smartphone-based assessment via DCNN accurately estimated MS-related disability. Severity scores strongly correlated with EDSS, but variability noted due to testing conditions.
Ellis et al., (45) NP Yes
Content
Criterion (concurrent)
(ANOVA: increased gait variability in PD-patients with medium to large effect sizes)
NP NP Yes, but only in clinical setting Highlight specific opportunities for smartphone-based gait analysis to serve as an alternative to conventional gait analysis methods (e.g., footswitch systems or sensorembedded walkways)
Ginis et al., (68) Test-retest
(ɳ² = 0.29. p < 0.001)
Inter/intra-rater reliability NP
NP NP NP Yes,but device placement unspecified CuPiD showed greater improvements in gait speed (9%) and dual-task speed (13.5%) compared to controls (5.2%, 5.8%).
Goñi et al., (75) NP NP 3.69% 99.42% Yes Gait metrics provided moderate classification performance between PD and HC.
Hamy et al., (34) Test-retest
(ICC = 0.86 - 0.91)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(r2 = 0.88, p < 0.001)
NP NP Yes Smartphone app demonstrated significant alignment with GAITRite measures (step length, step time).
He et al., (69) NP Yes
Content
Construct (discrimnativ)
(AUC = 0.883)
FNR = 0.053 NP Yes NeuroEnhanceNet achieved the highest AUC (0.883) and lowest FNR (0.053) for early PD detection.
Isho et al., (46) Test –retest
(ICC > 0.531 - 0.900)
Inter/intra-rater reliability NP
NP 72.7% 84.6% Yes Interstride variability of mediolateral acceleration is significantly associated with fall history; AUC = 0.745
Juen et al., (47) NP Yes
Content
Criterion (concurrent)
(ANOVA: F = 1.114e-4 (S5) and 9.36e-5 (Ace). p < 0.001;
no significant differences between MoveSense-App, Actigraph GT3X and „Ground Truth“)
NP NP Yes Strong alignment with Actigraph GT3X validated by ANOVA.
Kim et al., (20) NP NP Waist: 86%. Pocket: 84%. Ankle: 81% Waist: 91.7%. Pocket: 92.5%. Ankle: 91.5% Partial, placement consistency critical, noise from loose attachments Smartphone-based system detected FOG with high accuracy using acceleration and gyroscope data.
Lam et al., (78) Test –retest
(ICC = 0.764;
95% CI (0.651 - 0.845))
Inter/intra-rater reliability
NP
Yes
Content
Criterion (concurrent)
(Spearmans rank correlation coefficiant: p = -0.43 to -0.64)
Construct
(convergent)
(Mann–Whitney U. p < 0.05 for EDSS groups)
Moderate to strong correlation
with EDSS and
T25FW (ρ = -0.43 to -0.64)
AUC = 0.482 (95% CI [0.333. 0.632]);
insufficient for group-level distinction
Yes, but feasible for self-assessment but dependent on GPS signal quality; adherence decreased over time Group-level analyses lacked sensitivity to detect clinical changes due to variability, but individual-level curve fitting improved s2MWT reliability, identifying significant changes in walking function.
Lipsmeier et al., (70) Test –retest
(ICC = 0.80 for Gait)
Inter/intra-rater reliability
NP
NP Greater sensitivity than UPDRS NP Yes, feasible for home use; adherence of 61% in PD participants;
requires patient training
Smartphone-based assessments demonstrated excellent reliability and validity, detecting subtle PD motor impairments and correlating well with MDS-UPDRS ratings. Gait-related impairments were detected using passive monitoring.
Lopez et al., (48) Test –retest
(Wilcoxon, p = 0.0117)
Inter/intra-rater reliability
NP
NP NP NP Yes, but device placement unspecified; limited
generalizability due to small sample size
Gait metrics improved significantly with auditory cues: walking speed (+40.6%), cadence (+30.2%), and stride length (+50.3%) compared to baseline.
Mak et al., (49) Test –retest
(Cronbach´s Alpha = 0.74)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(Cronbach´s Alpha = 0.99)
69% 95% Yes High correlation between clinical and remote measurement; reliable for detecting frailty
Maldaner et al., (50) Test –retest
(ICC = 0.82;
SEM = 58.3 m)
Inter/intra-rater reliability NP
Yes
Content
Construct (convergent)
(Pearson correlation coefficients: moderate r = -0.31 - -0.42)
NP NP Yes, but only outside for GPS The smartphone app-based measurement of the 6WT is a convenient, reliable, and valid way to
determine objective functional impairment in patients with lumbar degenerative disc disease
Marom et al., (51) Test-retest
(ICC = 0.77 - 1)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(r = 0.65 - 1)
NP NP Yes The app showed good-to-excellent reliability and moderate-to-excellent validity for all parameters, except step length of impaired leg (poor-to-good).
Mehrang et al., (71) NP Yes
Content
Criterion (concurrent)
(Random forest classifier, accuracy = 70%)
70% 70% Yes Identification of PD via step parameters with 70% accuracy (random forest classifier)
Omberg et al., (30) NP Yes
Content
Criterion (concurrent)
(r = 0.71, p < 1.8×10⁻⁶ with UPDRS)
NP NP Yes Strong correlation between gait metrics collected remotely and UPDRS; While remote assessment demands careful interpretation of RWD, our findings support smartphones and wearables for objective, personalized disease evaluation
Pepa et al., (52) NP NP 85.6% for Algorithm 1 and 2 93.4% for Algorithm 1 and 2 Yes, but requires calibration Demonstrated high reliability and validity in measuring step length and cadence.
Pepa et al., (53) NP NP 84.9% for FoG detection 95.2% for FoG detection Yes, but requires calibration Demonstrated high validity and sensitivity in freezing of gait detection using fuzzy logic algorithms.
Polese et al., (54) NP Yes
Content
Criterion (concurrent)
(ICC = 0.93; CI: 0.86 - 0.96)
(r = 0.89, p < 0.001)
NP NP Yes Google Fit® application showed excellent agreement (ICC = 0.93) and high correlation with actual step counts.
Raknim et al., (76) NP NP 94% NP Yes, but only on Android Applying smartphone sensor data to provide early warnings to potential PD patients
Classification of changes in gait pattern with 94% accuracy for PD diagnoses
Regev et al., (55) NP Yes
Content
Construct (discriminative)
(χ² test, p < 0.05;
AUC = 85.65%)
Sensitivity 75.86%
(MS vs. HC. AUC = 85.65%)
Specificity 76.74%
(MS vs. HC. AUC = 85.65%)
Yes, but feasible in clinical settings; requires
standardized tasks; lacks real-world data
Digital markers differentiated MS patients from HC with AUC = 85.65%; correlations with EDSS (ρ = 0.55–0.65)
Rozanski et al., (82) NP Yes
Construct
(discrimnativ)
(g = 0.32 - 0.48)
NP NP Yes Active recordings showed higher stride length, velocity, and lower double support compared to passive recordings.
Salvi et al., (79) Test-retest
(ICC = 0.91; SEM = 36.97 m;
CoV: 12.45%)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(r = 0.89, p < 0.001)
NP NP Yes App measurements strongly correlated with physiologist-observed 6MWD (r = 0.89). ICC for repeatability was 0.91.
Schwab et al., (72) Test –retest NP
Inter/intra-rater reliability
NP
Yes
Content
Criterion (concurrent)
(AUC = 0.85; CI: 0.81 - 0.89)
43% 95% Yes Smartphone diagnostics achieved AUC of 0.85 with strong predictive performance for gait-based PD diagnosis.
Serra-Ano et al., (56) Test –retest
(ICC = 0.89 - 0.92 for gait)
Inter/intra-rater reliability
NP
NP NP NP Yes Reliable differentiation of postural and gait parameters between PD and HC groups.
Shema-Shiratzky et al., (57) Test –retest
(ICC = 0.460 - 0.997)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(95% LOA)
NP NP Partial High correlation for cadence and gait cycle time (r = 0.996-0.997), moderate correlation for stride length and bipedal support
Su et al., (77) NP Yes
Content
Criterion (concurrent)
(r = 0.99, p < 0.001 for stride time.
r = 0.98 - 0.99, p < 0.001 for stride time variability)
NP NP Yes Demonstrated excellent reliability and validity for stride time and stride time variability in PD patients.
Sugimoto et al., (35) NP Yes
Content
Criterion (concurrent)
(Group-by-limb interactions for sagittal-plane ankle kinematics F(1,42) = 63,786 p < 0.01;
Group-by-limb interactions for sagittal-plane average thigh angular range-of-motion F(1,42) = 6,166 p < 0.017)
NP NP Yes, but requires specific positioning of the device
on the thigh
AccWalker effectively detected differences in thigh RoM between RAS and healthy controls.
Tang et al., (36) Test-Retest-Reliability
(ICC 0.768 - 0.896)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(r = 0.858)
90.6% 94.3% Yes High consistency between smartphone and XSens; sensitivity and specificity good for FoG detection
Tao et al., (58) Test-retest:
(ICC: Thigh = 0.877–0.999;
Waist = 0.784–0.996)
Inter/intra-rater reliability
NP
Yes
Content
Criterion (concurrent)
(Regression analysis: p > 0.05 for most parameters (low/normal speed); no significant differences between the gait parameters of different gait velocitys)
NP NP Yes Reliable for healthy individuals and CSVD patients; higher reliability for thigh placement than waist.
Van Oirschot et al., (73) Test-retest
(ICC = 0.649)
Inter/intra-rater reliability NP
Yes
Content
Criterion (concurrent)
(ICC = 0.82)
NP NP Yes, but GPS accuracy and signal only outdoor The smartphone-based assessment provided a reliable and valid method for assessing gait speed and distance in persons with MS
It enabled remote monitoring and offered a user-friendly solution for capturing real-world functional mobility data
Wagner et al., (59) NP Yes
Content
Criterion (concurrent)
(Spearman’s rho for Pixel vs. observed steps = 0.141. p = 0.075); (Spearman’s rho for Samsung vs. observed steps = 0.033, p =
0.680)
NP NP Yes, but bad results with low walking speed Spearman correlations between Pixel and observed steps were weak (rho = 0.141), while Samsung showed minimal correlation (rho = 0.033). Accurate at moderate speeds; challenges at low walking speeds
Yahalom et al., (60) NP Yes
Content
Criterion (concurrent)
(F = 4.4 - 25.4. p < 0.05 for difference between PD and HC
NP NP Partial, requires controlled clinical setup, potential impact
of psychiatric conditions
Quantitative gait analysis was more sensitive than UPDRS for detecting NIP-related gait impairments.
Yahalom et al., (61) NP Yes
Content
Criterion (concurrent)
(r = 0.14 - 0.46, p < 0.05 for gait
NP NP Yes, but requires smartphone placement training;
accuracy depends on environmental factors
Reliable and valid for measuring stride length and cadence in PD patients under real-world and clinical conditions.
Zhai et al., (74) NP Yes
Content
Criterion (concurrent)
(ρ = 0.29, p = 0.022 for step/min)
57 % for varVM
75 % for steps/min
84 % for varVM
59 % for steps/min
Yes Smartphone-based accelerometry offers a more accurate assessment of mobility and disability in individuals with MS compared to wrist-worn accelerometers. Additionally, smartphones effectively differentiate between individuals with MS, healthy controls, and various stages or conditions of MS.
Abbreviations: Ace: Samsung Galaxy Ace, ANOVA: Analysis of variance, AUC: Area under the curve, CI: Confidence interval, CoV: Coefficient of Variation, DCNN: Deep convolutional neural networks, EDSS: Expanded disability status scale, FNR: False negative rate, FoG: freezing of gait, GPS: Global positioning system, HC: Healthy control, ICC: Intraclass correlation coefficient, LoA: Limits of agreement, MDS-UPDRS: Modified Unified Parkinson's Disease Rating Scale, MS: Multiple Sclerosis, NP: Not Provided, OT: Orthostatic tremor, PD: Parkinson disease, p: Statistical significance, r: Pearson correlation coefficient, SEM: Standard error of the mean, S2MWT: Smartphone-based 2 minute walking test, S5: Samsung Galaxy S5, T25FW: Timed 25-foot walk, UPDRS: Unified Parkinson's Disease Rating Scale, varVM: Variance of vector magnitude, VO2: Volume of oxygen, 2MWT: 2 minute walk test, 5UTT: 5 U-Turn test.
Table 3. Methodological quality assessment of the included studies.
Table 3. Methodological quality assessment of the included studies.
Author Question/
Objective
Population Participation
Rate
Selection/
recruitment
Exposure and outcome Timeframe
between
exposure and
outcome
Sample
size
Levels of
exposure
Exposure
measure
Repeated
exposure
measurement
Outcome
measure
Blinding of
outcome
assessors
Follow-up
rate
Statistical
analyses
Overall
quality
Abujrida et al., (62) Yes Yes Yes Yes No No No No Yes Yes Yes No No Yes Good
Adams et al., (37) Yes Yes Yes Yes No No Yes No Yes Yes Yes No No Yes Good
Alexander et al., (38) Yes Yes Yes Yes No No No No No No Yes No No Yes Fair
Arora et al., (29) No Yes No Yes No No Yes No Yes No Yes No No No Fair
Arora et al., (63) No Yes Yes Yes No No No Yes Yes Yes Yes No No No Fair
Balto et al., (39) Yes Yes Yes Yes No No No No Yes Yes Yes No No Yes Good
Banky et al., (33) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Bourke et al., (64) Yes Yes No Yes No No No No Yes No Yes No No Yes Good
Brinkløv et al., (81) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Brooks et al., (40) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Capecci et al., (41) Yes Yes No Yes No No Yes Yes Yes Yes Yes No No Yes Good
Chan et al., (80) Yes Yes No Yes No No Yes No Yes Yes Yes No No Yes Good
Chen et al., (65) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Cheng et al., (32) Yes Yes No Yes No No No No Yes No Yes No No Yes Good
Chien et al., (43) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Clavijo-Buendía et al., (31) Yes Yes Yes Yes No No Yes No Yes Yes Yes No No Yes Good
Costa et al., (44) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes Yes No Yes Good
Creagh et al., (67) Yes No No No Yes Yes No No Yes Yes Yes No No Yes Good
Creagh et al., (66) Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes No Yes Yes Good
Ellis et al., (45) Yes Yes No Yes No No Yes Yes Yes No Yes No No Yes Good
Ginis et al., (68) Yes Yes Yes Yes No No Yes Yes Yes No Yes No Yes Yes Good
Goñi et al., (75) Yes Yes Yes Yes No No Yes Yes Yes No Yes No No Yes Good
Hamy et al., (34) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
He et al., (69) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes Yes Yes Yes Good
Isho et al., (46) Yes Yes No No No No Yes No Yes Yes No No No Yes Fair
Juen et al., (47) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Kim et al., (20) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Lam et al., (78) Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes No Yes Yes Good
Lipsmeier et al., (70) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Lopez et al., (48) Yes Yes Yes Yes No No Yes Yes Yes No Yes Yes No Yes Good
Mak et al., (49) Yes Yes Yes Yes No No Yes No Yes Yes Yes No No Yes Good
Maldaner et al., (50) Yes Yes Yes Yes No No Yes No Yes No No No No Yes Good
Marom et al., (51) Yes Yes Yes Yes No No Yes Yes Yes No Yes No No Yes Good
Mehrang et al., (71) Yes Yes Yes Yes No No Yes No Yes No Yes No No No Good
Omberg et al., (30) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Pepa et al., (52) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Pepa et al., (53) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Polese et al., (54) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes Yes No Yes Good
Raknim et al., (76) Yes Yes No Yes Yes Yes Yes Yes Yes Yes Yes No Yes Yes Good
Regev et al., (55) Yes Yes Yes Yes No No Yes Yes Yes No Yes No No Yes Good
Rozanski et al., (82) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Salvi et al., (79) Yes Yes Yes Yes Yes Yes No Yes Yes Yes Yes No No Yes Good
Schwab et al., (72) Yes Yes Yes Yes No No Yes Yes Yes No Yes No No Yes Good
Serra-Ano et al., (56) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Shema-Shiratzky et al., (57) Yes Yes Yes Yes No No Yes No Yes Yes Yes No No Yes Good
Su et al., (77) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Sugimoto et al., (35) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Tang et al., (36) Yes Yes Yes Yes No No Yes No Yes Yes Yes No No Yes Good
Tao et al., (58) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Van Oirschot et al., (73) Yes Yes Yes Yes No No Yes No Yes Yes Yes No No Yes Good
Wagner et al., (59) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Yahalom et al., (60) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Yahalom et al., (61) Yes Yes Yes Yes No No Yes Yes Yes Yes Yes No No Yes Good
Zhai et al., (74) Yes Yes Yes Yes No No No No Yes No Yes No No Yes Good
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