Clinical Trial: Prospective Longitudinal Monocentric Study to Evaluate the Feasibility of Syde(R) Digital Endpoints for Monitoring Patients With Progressive Supranuclear Palsy - Richardson Syndrome (PSP-R)

U.S., Feb. 6 -- ClinicalTrials.gov registry received information related to the study (NCT07389018) titled 'Prospective Longitudinal Monocentric Study to Evaluate the Feasibility of Syde(R) Digital Endpoints for Monitoring Patients With Progressive Supranuclear Palsy - Richardson Syndrome (PSP-R)' on Jan. 28.

Brief Summary: The study aims to assess the feasibility/acceptability of real-world activity monitoring by the Syde(R) wearable device in PSP-R. The Syde(R) collected data will be compared to on-site conventional clinical endpoints, including functional capacity and cognitive assessments, as well as core scales assessments.

Study Start Date: Feb., 2026

Study Type: OBSERVATIONAL

Condition: Progressive Supranuclear Palsy- Richardson...