The Cerebral Palsy Research Registry: Development and Progress Toward National collaboration in the United States

Donna S. Hurley*, Theresa Sukal-Moulton, Michael E. Msall, Deborah Gaebler-Spira, Kristin J. Krosschell, Julius P. Dewald

*Corresponding author for this work

Research output: Contribution to journalArticle

26 Scopus citations

Abstract

Cerebral palsy is the most common neurodevelopmental motor disability in children. The condition requires medical, educational, social, and rehabilitative resources throughout the life span. Several countries have developed population-based registries that serve the purpose of prospective longitudinal collection of etiologic, demographic, and functional severity. The United States has not created a comprehensive program to develop such a registry. Barriers have been large population size, poor interinstitution collaboration, and decentralized medical and social systems. The Cerebral Palsy Research Registry was created to fill the gap between population and clinical-based cerebral palsy registries and promote research in the field. This is accomplished by connecting persons with cerebral palsy, as well as their families, to a network of regional researchers. This article describes the development of an expandable cerebral palsy research registry, its current status, and the potential it has to affect families and persons with cerebral palsy in the United States and abroad.

Original languageEnglish (US)
Pages (from-to)1534-1541
Number of pages8
JournalJournal of child neurology
Volume26
Issue number12
DOIs
StatePublished - Dec 2011

Keywords

  • cerebral palsy
  • registries
  • research

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

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