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Consensus Guidelines for Improving Quality of Assessment and Training for Neuromuscular Diseases

Authors :
Tina Duong
Kristin J. Krosschell
Meredith K. James
Leslie Nelson
Lindsay N. Alfano
Katy Eichinger
Elena Mazzone
Kristy Rose
Linda P. Lowes
Anna Mayhew
Julaine Florence
Wendy King
Claudia R. Senesac
Michelle Eagle
Source :
Frontiers in Genetics, Vol 12 (2021), Frontiers in Genetics
Publication Year :
2021
Publisher :
Frontiers Media SA, 2021.

Abstract

Critical components of successful evaluation of clinical outcome assessments (COAs) in multisite clinical trials and clinical practice are standardized training, administration, and documented reliability of scoring. Experiences of evaluators, alongside patient differences from regional standards of care, may contribute to heterogeneity in clinical center’s expertise. Achieving low variability and high reliability of COA is fundamental to clinical research and to give confidence in our ability to draw rational, interpretable conclusions from the data collected. The objective of this manuscript is to provide a framework to guide the learning process for COAs for use in clinics and clinical trials to maximize reliability and validity of COAs in neuromuscular disease (NMD). This is a consensus-based guideline with contributions from fourteen leading experts in clinical outcomes and the field of clinical outcome training in NMD. This framework should guide reliable and valid assessments in NMD specialty clinics and clinical trials. This consensus aims to expedite study start up with a progressive training pathway ranging from research naïve to highly experienced clinical evaluators. This document includes recommendations for education guidelines and roles and responsibilities of key stakeholders in COA assessment and implementation to ensure quality and consistency of outcome administration across different settings.

Details

Language :
English
ISSN :
16648021
Volume :
12
Database :
OpenAIRE
Journal :
Frontiers in Genetics
Accession number :
edsair.doi.dedup.....a405760155bd0130de4fe43bffb2fcd5
Full Text :
https://doi.org/10.3389/fgene.2021.735936