Partnership with participants on study protocols and conduct informs study design, provides novel insights, and speeds enrollment and outcomes. The Parkinson's Progression Markers Initiative (PPMI) solicits volunteer inputs through a Community Advisory Board, in-person events, and communication with site teams and centralized study services. Participant inputs have shaped PPMI procedures and protocols including (i) the myPPMI online platform, (ii) return of research information, (iii) lumbar puncture education, (iv) engaging representative populations, and (v) travel procedures. The study's methods for engaging participants and its modifications arising from those conversations provide a model for those seeking to design accessible and impactful studies. ANN NEUROL 2026.
Building similarity graph...
Analyzing shared references across papers
Loading...
Maggie Kuhl
Michael J. Fox Foundation
Christina Destro
Michael J. Fox Foundation
Roseanne D. Dobkin
Johnson University
Annals of Neurology
University of Pennsylvania
Indiana University – Purdue University Indianapolis
Indiana University School of Medicine
Building similarity graph...
Analyzing shared references across papers
Loading...
Kuhl et al. (Tue,) studied this question.
synapsesocial.com/papers/69e9bb2285696592c86eceed — DOI: https://doi.org/10.1002/ana.78220
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: