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by xavier.grehant on 2026-05-17

Digital biomarkers Tremor Trial design & recruitment

Researchers at Radboud University Medical Centre in the Netherlands asked 620 people with early-stage Parkinson's disease to wear a research smartwatch around the clock for two years — part of the large Personalized Parkinson Project. A custom algorithm analysed the raw wrist-movement data to extract two weekly measures: tremor time (how often the person was shaking) and tremor power (how intense the shaking was). These continuous, real-world readings were then compared against the standard clinical yardstick — the MDS-UPDRS (Movement Disorder Society–Unified Parkinson's Disease Rating Scale), a structured assessment done by a neurologist in clinic, typically once a year. This is an observational, longitudinal study — not a treatment trial — so it tells us what can be measured, not what can be treated.

The headline finding: among participants who had not yet started dopaminergic medication (drugs that replace or mimic dopamine), the smartwatch measures were substantially more sensitive to worsening tremor over the two-year period than annual clinical scores. Put simply, the watch picked up progression that a yearly hospital exam would miss or detect much later. In medicated participants the picture is more complex, because medication partially suppresses tremor and dose changes affect the sensor readings too — the researchers analysed these groups separately for exactly that reason. Crucially, the algorithm and its source code are freely available, and the method works on many standard research-grade wearables, not a proprietary device.

For people living with Parkinson's and their families, the immediate implication is indirect but meaningful: this kind of tool could make future clinical trials faster and smaller, because researchers could detect whether a new disease-modifying drug is working much sooner than with annual clinic visits. It could also, in the longer term, help neurologists personalise care — monitoring whether a medication dose is actually helping at home rather than only during a brief, potentially stressful clinic appointment. The technology is not yet a routine clinical tool; further work is needed to validate it across different devices and care settings. But it represents a genuine step forward in the field of digital biomarkers — objective, continuous measurements of how the disease is progressing in real life.

What this article adds

Digital biomarkers
This two-year observational study of 540 early-PD participants (Personalized Parkinson Project) showed that continuous wrist-sensor measures of tremor time and tremor power were substantially more sensitive to disease progression than annual MDS-UPDRS clinical scores, particularly in unmedicated patients — the largest and longest real-world validation of wearable tremor monitoring in PD to date.
Tremor
Continuous smartwatch data capturing how often and how intensely tremor occurs in daily life detected two-year worsening that standard yearly clinic assessments largely missed; the gap in sensitivity was especially pronounced before dopaminergic medication was started, clarifying how tremor progresses in the real world versus the clinic snapshot.
Trial design & recruitment
Because the sensor-derived tremor measures are far more sensitive to change than annual clinical ratings, adopting them as outcome measures in early-PD trials could meaningfully reduce the sample size or follow-up time needed to detect whether a disease-modifying treatment is working — a practical advance for trial design.

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