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Updated: Sep 3, 2026

Dynamic Digital Biomarkers of Motor and Cognitive Function in Parkinson's Disease
Published on: July 24, 2019
Optimising fall risk classification models in Parkinson's disease using clinical and mobility outcomes
Marta Mirando1, Silvia Del Din2, Rana Zia Ur Rehman3
1Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK; Department of Clinical-Surgical, Diagnostic and Paediatric Sciences, University of Pavia, Pavia, Italy; Newcastle NIHR Biomedical Research Centre, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
Background:
Falls are a serious concern in Parkinson's disease (PD), often leading to hospitalisation, dependence and reduced quality of life. Effective fall management requires identification of those at risk. This cross-sectional, discriminative study aimed to evaluate which selection of outcomes best discriminate retrospective fallers from non-fallers, to inform a future prospective clinical prediction tool.
Methods:
People with PD were recruited (ICICLE-GAIT; 54- and 72-month follow up assessments). Fallers and non-fallers were stratified based on prospective fall reports. A total of 299 outcomes across 4 domains were collected: clinical (n = 9), lab-based mobility (gait n = 60, turning n = 99), real-world mobility (n = 131). Receiver operating characteristic analysis evaluated classification models distinguishing fallers from non-fallers. Area under the curve (AUC) determined which models were optimal. Models were re-applied at 72-months.
Results:
Of the 48 participants, 32 (67%) were classified as fallers and 16 (33%) as non-fallers. Significant group differences (faller vs. non-faller) were found in all domains at 54-months; clinical (n = 2/9), lab-based gait (n = 8/60), lab-based turning (n = 19/99) and real-world mobility (n = 5/131). At 54-months, turning was the strongest single-domain model (apparent AUC = 0.86, sensitivity = 0.74, specificity = 0.93; optimism-corrected AUC = 0.61), followed by real-world mobility (AUC = 0.82, sensitivity = 0.68, specificity = 1.00; optimism-corrected AUC = 0.72). All multi-domain combinations including turning showed acceptable discrimination, with AUC values > 0.70. At 72-months, turning alone retained apparent perfect discrimination (AUC = 1.00), whereas clinical (AUC = 0.52), gait (AUC = 0.51) and real-world (AUC = 0.69) models declined substantially.
Conclusion:
Turning showed strong discriminative power in classifying PD fallers remaining robust over time and outperforming other assessments. Real-world mobility also had strong discriminative value, highlighting the importance of ecologically valid continuous monitoring. As this study was discriminative and exploratory in nature, these findings should be interpreted as hypothesis-generating pending external validation. Future models should explore whether real-world turning provides superior discriminative value to lab-based turning.
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