A common data language for clinical research studies: the National Institute of Neurological Disorders and Stroke and American Academy for Cerebral Palsy and Developmental Medicine Cerebral Palsy Common Data Elements Version 1.0 recommendations.

Publication Type
Journal Article
Year of Publication
2018
Authors
Schiariti, VerĂ³nica; Fowler, Eileen; Brandenburg, Joline E; Levey, Eric; Mcintyre, Sarah; Sukal-Moulton, Theresa; Ramey, Sharon L; Rose, Jessica; Sienko, Susan; Stashinko, Elaine; Vogtle, Laura; Feldman, Robin S; Koenig, James I
Secondary
Dev Med Child Neurol
Volume
60
Start Page
976
Pagination
976-986
Date Published
10/2018
Keywords
Biomedical Research; Cerebral Palsy; common data elements; Guidelines as Topic; Humans; National Institute of Neurological Disorders and Stroke (U.S.); Societies, Medical; United States
Abstract

To increase the efficiency and effectiveness of clinical research studies, cerebral palsy (CP) specific Common Data Elements (CDEs) were developed through a partnership between the National Institute of Neurological Disorders and Stroke (NINDS) and the American Academy of Cerebral Palsy and Developmental Medicine (AACPDM). International experts reviewed existing NINDS CDEs and tools used in studies of children and young people with CP. CDEs were compiled, subjected to internal review, and posted online for external public comment in September 2016. Guided by the International Classification of Functioning, Disability and Health framework, CDEs were categorized into six domains: (1) participant characteristics; (2) health, growth, and genetics; (3) neuroimaging; (4) neuromotor skills and functional assessments; (5) neurocognitive, social, and emotional assessments; and (6) engagement and quality of life. Version 1.0 of the NINDS/AACPDM CDEs for CP is publicly available on the NINDS CDE and AACPDM websites. Global use of CDEs for CP will standardize data collection, improve data quality, and facilitate comparisons across studies. Ongoing collaboration with international colleagues, industry, and people with CP and their families will provide meaningful feedback and updates as additional evidence is obtained. These CDEs are recommended for NINDS-funded research for CP.

WHAT THIS PAPER ADDS: This is the first comprehensive Common Data Elements (CDEs) for children and young people with CP for clinical research. The CDEs for children and young people with CP include common definitions, the standardization of case report forms, and measures. The CDE guides the standardization for data collection and outcome evaluation in all types of studies with children and young people with CP. The CDE ultimately improves data quality and data sharing.

Comment in

A common data language for clinical research studies: the art and science of uncertainty. [Dev Med Child Neurol. 2018] https://www.ncbi.nlm.nih.gov/pubmed/29707765