Digital Health Technologies for Progressive Supranuclear Palsy and Dementia With Lewy Bodies

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age40-89
SponsorBioSensics

About this trial

Progressive supranuclear palsy (PSP), mild cognitive impairment with Lewy bodies (MCI-LB), and Dementia with Lewy Bodies (DLB) are severe neurodegenerative diseases that cause significant motor impairment impacting daily function. Researchers at BioSensics, Johns Hopkins School of Medicine, Massachusetts General Hospital and their collaborators aim to conduct an analytical and clinical validation of wearable-based digital health technologies for monitoring upper and lower limb function in PSP, MCI-LB and DLB that could enable frequent, at-home monitoring and be incorporated into future clinical trials.

Eligibility criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

60 Participants
are grouped into 2 trial groups

Sponsors and collaborators

BioSensics

Lead sponsor

National Institute on Aging (NIA)

Collaborator

Johns Hopkins University

Collaborator

Massachusetts General Hospital

Collaborator