TY - JOUR
T1 - The future of clinical trials?
T2 - Monitoring mobility as an outcome measure in Parkinson's disease: The mobilise-D study
AU - Yarnall, Alison J
AU - Alcock, Lisa
AU - Schlenstedt, Christian
AU - Armengol, Claudia
AU - Becker, Clemens
AU - Brown, Philip
AU - Buekers, Joren
AU - Caulfield, Brian
AU - Cereatti, Andrea
AU - Cordova-Rivera, Laura
AU - Del Din, Silvia
AU - Delgado-Ortiz, Laura
AU - Forrest-Gordon, Mark
AU - Garcia-Aymeriche, Judith
AU - Goerrissen, Pia
AU - Hansen, Clint
AU - Hildesheim, Hanna
AU - Hiden, Hugo
AU - Hunter, Heather
AU - Jansen, Carl-Philipp
AU - Koch, Sarah
AU - Kudelka, Jennifer
AU - Long, Michael
AU - Neatrour, Isabel
AU - Sharrack, Basil
AU - Singleton, David
AU - Sutcliffe, Lou
AU - Troosters, Thierry
AU - Winkler, Juergen
AU - Ginis, Pieter
AU - Gassner, Heiko
AU - Nieuwboer, Alice
AU - Hausdorff, Jeffrey M
AU - Mirelman, Anat
AU - Rochester, Lynn
AU - Maetzler, Walter
PY - 2026/2/1
Y1 - 2026/2/1
N2 - BackgroundA key challenge in trials targeting disease modification in Parkinson's disease (PD) is the lack of sensitive, precise, and patient-relevant outcome measures. Digital mobility outcomes (DMOs), captured using body-worn devices, offer a novel, objective means to assess real-world gait and mobility-domains often impaired early in PD. The Mobilise-D consortium was established to develop and validate DMOs in PD and other conditions.ObjectiveTo describe DMOs in a large, representative international cohort of individuals with PD and compare to controls and across disease stage; and to determine compliance and feasibility.MethodsAs part of the Mobilise-D Clinical Validation and Extension Studies, real-world mobility of individuals with PD (n = 601) and matched controls (n = 232) was assessed using a single wearable device for seven days. Data were processed to yield 24 technically validated DMOs, representing different domains of real-world walking and mobility performance.ResultsDMO data were available for 531 PD and 221 controls. Significant differences between the groups were observed in 20 of 24 DMOs. Compared to controls, PD participants exhibited shorter daily walking duration and lower step counts, walking at a higher cadence and in fewer walking bouts per day. Findings also varied by disease severity, with differences observed particularly between controls vs. mild (Hoehn and Yahr stage I-II) and mild vs. moderate (Hoehn and Yahr stage III) disease. Compliance rates were high.ConclusionsDistinct DMO patterns across PD severity and between PD and controls support their utility as sensitive, scalable outcome measures for future clinical trials and therapeutic development.
AB - BackgroundA key challenge in trials targeting disease modification in Parkinson's disease (PD) is the lack of sensitive, precise, and patient-relevant outcome measures. Digital mobility outcomes (DMOs), captured using body-worn devices, offer a novel, objective means to assess real-world gait and mobility-domains often impaired early in PD. The Mobilise-D consortium was established to develop and validate DMOs in PD and other conditions.ObjectiveTo describe DMOs in a large, representative international cohort of individuals with PD and compare to controls and across disease stage; and to determine compliance and feasibility.MethodsAs part of the Mobilise-D Clinical Validation and Extension Studies, real-world mobility of individuals with PD (n = 601) and matched controls (n = 232) was assessed using a single wearable device for seven days. Data were processed to yield 24 technically validated DMOs, representing different domains of real-world walking and mobility performance.ResultsDMO data were available for 531 PD and 221 controls. Significant differences between the groups were observed in 20 of 24 DMOs. Compared to controls, PD participants exhibited shorter daily walking duration and lower step counts, walking at a higher cadence and in fewer walking bouts per day. Findings also varied by disease severity, with differences observed particularly between controls vs. mild (Hoehn and Yahr stage I-II) and mild vs. moderate (Hoehn and Yahr stage III) disease. Compliance rates were high.ConclusionsDistinct DMO patterns across PD severity and between PD and controls support their utility as sensitive, scalable outcome measures for future clinical trials and therapeutic development.
KW - biomarkers
KW - clinical trials
KW - gait disorders
KW - patient-reported outcomes
KW - technology
KW - wearable technology
UR - https://www.scopus.com/pages/publications/105029620173
U2 - 10.1177/1877718X251407026
DO - 10.1177/1877718X251407026
M3 - Article
C2 - 41452018
SN - 1877-7171
VL - 16
SP - 110
EP - 124
JO - Journal of Parkinson's Disease
JF - Journal of Parkinson's Disease
IS - 1
ER -