Literature DB >> 29542813

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.

Verónica Schiariti1,2, Eileen Fowler3, Joline E Brandenburg4, Eric Levey5, Sarah Mcintyre6, Theresa Sukal-Moulton7, Sharon L Ramey8, Jessica Rose9, Susan Sienko10, Elaine Stashinko11, Laura Vogtle12, Robin S Feldman13, James I Koenig14.   

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.
© 2018 Mac Keith Press.

Entities:  

Mesh:

Year:  2018        PMID: 29542813     DOI: 10.1111/dmcn.13723

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  13 in total

Review 1.  A Critical Evaluation of Current Concepts in Cerebral Palsy.

Authors:  Joline E Brandenburg; Matthew J Fogarty; Gary C Sieck
Journal:  Physiology (Bethesda)       Date:  2019-05-01

2.  Eating and Drinking Ability Classification System.

Authors:  Diane Sellers
Journal:  Dysphagia       Date:  2018-09-19       Impact factor: 3.438

3.  Reliability and Validity of the Eating and Drinking Ability Classification System in Adults with Cerebral Palsy.

Authors:  Sung Eun Hyun; You Gyoung Yi; Hyung-Ik Shin
Journal:  Dysphagia       Date:  2020-06-09       Impact factor: 3.438

4.  Core Data Elements in Acute Myeloid Leukemia: A Unified Medical Language System-Based Semantic Analysis and Experts' Review.

Authors:  Christian Holz; Torsten Kessler; Martin Dugas; Julian Varghese
Journal:  JMIR Med Inform       Date:  2019-08-12

5.  Cerebral Palsy Research Network Clinical Registry: Methodology and Baseline Report.

Authors:  Paul Gross; Mary Gannotti; Amy Bailes; Susan D Horn; Jacob Kean; Unni G Narayanan; Jerry Oakes; Garey Noritz
Journal:  Arch Rehabil Res Clin Transl       Date:  2020-04-19

6.  Early intervention service intensity and young children's home participation.

Authors:  M A Khetani; B M McManus; E C Albrecht; V C Kaelin; J K Dooling-Litfin; E A Scully
Journal:  BMC Pediatr       Date:  2020-07-03       Impact factor: 2.125

7.  Implementation of the International Classification of Functioning, Disability, and Health (ICF) Core Sets for Children and Youth with Cerebral Palsy: Global Initiatives Promoting Optimal Functioning.

Authors:  Verónica Schiariti; Egmar Longo; Alexander Shoshmin; Ludmila Kozhushko; Yanina Besstrashnova; Maria Król; Taynah Neri Correia Campos; Haryelle Náryma Confessor Ferreira; Cláudia Verissimo; Daniel Shaba; Matilda Mwale; Sandra Amado
Journal:  Int J Environ Res Public Health       Date:  2018-09-01       Impact factor: 3.390

8.  Cerebral palsy information system with an approach to information architecture: a systematic review.

Authors:  Mina Afzali; Korosh Etemad; Alireza Kazemi; Reza Rabiei
Journal:  BMJ Health Care Inform       Date:  2019-12

9.  The Influence of Hippotherapy on the Body Posture in a Sitting Position among Children with Cerebral Palsy.

Authors:  Ewelina Matusiak-Wieczorek; Elzbieta Dziankowska-Zaborszczyk; Marek Synder; Andrzej Borowski
Journal:  Int J Environ Res Public Health       Date:  2020-09-19       Impact factor: 3.390

10.  Pilot implementation of an electronic patient-reported outcome measure for planning and monitoring participation-focused care in early intervention.

Authors:  E C Albrecht; V C Kaelin; B L Rigau; J K Dooling-Litfin; E A Scully; N J Murphy; B M McManus; M A Khetani
Journal:  BMC Med Inform Decis Mak       Date:  2020-08-24       Impact factor: 2.796

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