Status: Not yet recruiting
Study to Evaluate the Feasibility of Syde® Digital Endpoints for Monitoring Patients With Progressive Supranuclear Palsy - Richardson Syndrome (PSP-R)
The study aims to assess the feasibility/acceptability of real-world activity monitoring by the Syde® wearable device in PSP-R. The Syde® collected data will be compared to on-site conventional clinical endpoints, including functional capacity and cognitive assessments, as well as core scales assessments.
Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: SYSNAVUpdated: Apr 22, 2026Locations: 1
Eligibility criteria
Patients with extreme cognitive disorders that limit their understanding of the... [+6]