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Core Health Outcomes In Childhood Epilepsy (CHOICE): protocol for the selection of a core outcome set

Christopher Morris1, Colin Dunkley2, Frances M Gibbon3

  • 1Peninsula Cerebra Research Unit (PenCRU) & NIHR Collaboration for Leadership in Applied Health Research and Care South West Peninsula (PenCLAHRC), University of Exeter Medical School, Exeter, UK. Christopher.Morris@exeter.ac.uk.

Trials
|November 30, 2017
PubMed

Insights

This study aims to develop a core outcome set for childhood epilepsy research. It will involve patients, families, and professionals to ensure relevant outcomes are measured for better health interventions.

Area of Science:

  • Pediatric Neurology
  • Clinical Trial Methodology
  • Health Outcomes Research

Background:

  • Establishing core outcome sets enhances the utility of health research.
  • Currently, no core outcome set exists for childhood epilepsy.
  • This work focuses on rolandic epilepsy as a model for developing a core outcome set for childhood epilepsy syndromes.

Framework:

  • Identify and define key outcomes for childhood epilepsy interventions.
  • Determine standardized methods for measuring these outcomes.
  • Engage diverse stakeholders, including young people with epilepsy and their families.

Implementation:

  • Conduct a multi-round Delphi survey with families, charities, and health professionals.
  • Seek consensus on outcome domains and their importance.
  • Convene a face-to-face meeting to ratify the core outcome set.

Implications:

  • The developed methodology offers a pragmatic approach to creating a core outcome set for childhood epilepsy.
  • This will facilitate more consistent and useful evaluative research for childhood epilepsy interventions.
  • Recommendations for outcome measurement using clinical assessments and patient-reported outcomes will be provided.
Abstract

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