NCT07240805 · NOT YET RECRUITING
Digital Health Technologies for Progressive Supranuclear Palsy and Dementia With Lewy Bodies
This study is testing wearable sensor devices to track movement and physical function in people already diagnosed with Progressive Supranuclear Palsy, MCI with Lewy bodies, or Dementia with Lewy bodies. Researchers want to know whether these wearables can reliably capture how limbs are working day-to-day, at home, without clinic visits. The phase is unspecified, meaning this is likely a validation or observational study, not a drug or treatment trial.
You may qualify if
- Male and female participants aged 40-89 meeting clinical diagnostic criteria for probable PSP, probable MCI-LB or probable DLB.
- Able to be present for all study procedures, complete questionnaires and assist during home data collection.
- Eligible participants must be fluent in reading and speaking English and must be capable of providing informed consent based on the principal investigator's judgment.
- Must have a caregiver or study partner who is willing and able to assist with all study-related procedures.
- Ambulatory (able to take 10 steps with minimal support such as use of a cane)
You're excluded if
- Any neurological, medical, or psychiatric condition that would preclude or confound participation in study activities based on the investigator's judgment.
- History of frequent falls defined as more than 5 falls per month, will not be eligible to participate in the study.
The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.
Eligibility criteria as of 2026-04-09