- Wearable for Assessing Tremor and Continuous Health in Parkinson’s Disease and Essential Tremor — Recruiting • Neurology • NCT07787299.
- What is being tested: Non-invasive wearable sensors are being evaluated to measure tremor and upper-limb movement patterns in adults with Parkinson's disease or essential tremor, with monitoring periods ranging from 3 to 21 days in both clinic and home settings.
- Patient eligibility overview: The study recruits adults diagnosed with either Parkinson's disease or essential tremor who are capable of attending an initial clinic visit and subsequently wearing the sensors during follow-up periods.
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
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.
- : 1. Aged 18 years or older. 2. Clinical diagnosis of idiopathic Parkinson's disease (Hoehn and Yahr stage I-III) or essential tremor. 3. Motor or tremor symptoms confirmed on clinical assessment. 4. Able to walk at least 4 metres independently, with or without a walking aid. 5. Able to provide written informed consent and comply with study procedures. 6. Willing and able to wear the study sensors in clinic and, where applicable, at home. 7. Able to understand study information and complete study materials in English.
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.