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Wearable for Assessing Tremor and Continuous Health in Parkinson's Disease and Essential Tremor

NCT07787299 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2026-08-31

No results posted yet for this study

Summary

This prospective observational study will examine tremor and upper-limb movement in adults with Parkinson's disease or essential tremor using non-invasive wearable sensors. Participants will attend one clinic visit and may then wear sensors at home for 3, 7, or 21 days. Clinic assessments will be scheduled around participants' usual medication times; the study will not change or delay treatment. Sensor data will be analysed offline for research and will not be used to make clinical decisions.

Conditions

  • PARKINSON DISEASE (Disorder)

Interventions

DEVICE

Device exposure: Wearable inertial sensor monitoring

PD-WATCH and comparator wearable sensors are used only to collect research data. Both cohorts continue their usual medication and clinical care; no treatment is assigned or changed by the study.

Sponsors & Collaborators

  • NHS Lothian

    collaborator OTHER_GOV

  • Heriot-Watt University

    lead OTHER

Principal Investigators

  • Anne Bernassau · Heriot-Watt University

  • Gordon Duncan · NHS Lothian

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-09-01
Primary Completion
2027-12-31
Completion
2027-12-31

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07787299 on ClinicalTrials.gov