Increasing Patient Self-Enrollment in the National Amyotrophic Lateral Sclerosis Registry: Lessons Learned From a Direct to Provider Campaign

Objective: To conduct educational and promotional outreach activities to general neurologists and to increase self-enrollment of persons with amyotrophic lateral sclerosis (ALS) in the National ALS Registry (Registry). Methods: A multicomponent project to educate neurologists and increase Registry s...

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Detalles Bibliográficos
Main Authors: Lindsay Rechtman DrPH, Heather Jordan MPH, Wendy Kaye PhD, Maggie Ritsick MPH, Paul Mehta MD
Formato: Artigo
Idioma:English
Publicado: SAGE Publishing 2020-02-01
Series:Journal of Patient Experience
Acceso en liña:https://doi.org/10.1177/2374373518811935