A Wearable Sensor Platform for Remote Monitoring of Individuals on the Frontotemporal Dementia Spectrum
Part of paid clinical trials in Lutherville, Maryland.
- Sponsor
- BioSensics
- Study ID
- NCT07569367
- Status
- Not Yet Recruiting
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Conditions
- Corticobasal Degeneration
- Corticobasal Syndrome (CBS)
- Frontotemporal Dementia (FTD)
- Frontotemporal Lobar Degeneration (FTLD)
Eligibility Criteria
- Sex
- ALL
- Age
- 40 Years - N/A
- Healthy Volunteers
- Not accepted
Study Details
The primary objective of this clinical study is to provide the initial validation for monitoring biomarkers of symptoms and functioning for individuals with frontotemporal lobar degeneration (FTLD) syndromes. Researchers at BioSensics, Johns Hopkins University School of Medicine, and Massachusetts General Hospital will use wearable sensors, computerized speech, psychomotor, and cognitive assessments to create outcome measures and digital biomarkers for FTLD syndromes. Researchers will deploy this digital health solution to monitor 60 patients with FTLD syndromes for 24 months with study visits every 6 months.
Key Dates
- Start date
- Aug 1, 2026
- Status verified
- Apr 2026
- Primary completion
- Aug 15, 2030
- Completion
- Dec 15, 2030
Study Design
- Enrollment
- 60 participants (estimated)
Arms
- Arm: Frontotemporal Lobar Degeneration (FTLD)60 patients who have a clinical diagnosis of possible or probable FTLD syndrome phenotype.
Primary Outcome Measure
Physical Activity Monitoring [ Time Frame: 24 months ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Johns Hopkins University School of Medicine | Lutherville | Maryland | 21093 | Alexander Pantelyat, MD (PRINCIPAL_INVESTIGATOR) |
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | Anne-Marie Wills, MD,MPH (PRINCIPAL_INVESTIGATOR) |
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