A Multi-Modal Remote Monitoring Platform for Frontotemporal Lobar Degeneration (FTLD) Syndromes
Running, not enrolling
Conditions studied: PSP, CBD, Progressive Supranuclear Palsy, FTD, Corticobasal Degeneration, Frontotemporal Dementia, Frontotemporal Lobar Degeneration
In brief
The primary objective of this study is to enroll an observational cohort of approximately 60 patients with PSP over the course of 24 months using a multicenter study design and to follow each of them for 12 months. The secondary objective of this study is to develop a robust solution for multi-modal remote monitoring of motor symptoms and function in PSP that can be applied to other Frontotemporal lobar degeneration (FTLD) syndromes.
Key facts
- Study ID
- NCT05956834
- Run by
- Massachusetts General Hospital
- People needed
- 60
- Starts
- 2023-07-28
- Expected to finish
- 2027-12-30
- Last updated by the study team
- 2026-01-21
Who can join
Age: 40 and older, up to 89. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinical diagnosis of possible or probable PSP as defined by the 2017 MDS criteria
- Fluent in reading and speaking English and capable of providing informed consent based on the principal investigator's judgement
- Able to walk 10 feet unassisted at the time of initial enrollment
- Must have a caregiver or study partner who is willing and able to assist with all study-related procedures
You may not qualify if…
- Any neurological, medical, or psychiatric condition that would preclude participation in study activities based on the investigator's judgment.
- A history of frequent falls defined as more than 5 falls per month, or who require a walker to ambulate safely at baseline will not be eligible to participate in the study.
Where it is running
- Johns Hopkins School of Medicine — Baltimore, Maryland, United States
- Massachusetts General Hospital — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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