3 results
Establish the technical feasibility and safety of implantation of the investigational device, adjustment of the investigational device post-implantation and the ability of the investigational device to reduce mitral valve regurgitation.
Primary ObjectiveTo generate evidence demonstrating the domain specification (via modern psychometric methods), reliability, validity, and responsiveness (within-subject meaningful change) of the patient-reported outcome (PRO) endpoints Secondary…
1. To study the differential effectiveness of three cueing modalities on gait parameters, gait stability, and interlimb coordination in people with Parkinson's disease 2. To study the differences between self-selected and a 10% increased cueing…