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Validation of the Seizure-Related Impact Assessment Scale (SERIAS): a study protocol.
Foster, Emma; Conquest, Alison; Ewart, Chris; Nicolo, John-Paul; Rayner, Genevieve; Winton-Brown, Toby; O'Brien, Terence J; Kwan, Patrick; Malpas, Charles; French, Jacqueline A.
Afiliação
  • Foster E; Department of Neurology, Alfred Health, Prahran, Victoria, Australia emma.foster@monash.edu.
  • Conquest A; School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
  • Ewart C; Department of Neurology, Alfred Health, Prahran, Victoria, Australia.
  • Nicolo JP; School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
  • Rayner G; Community and Research Engagement (CaRE) Program, Monash University, Clayton, Victoria, Australia.
  • Winton-Brown T; Department of Neurology, Alfred Health, Prahran, Victoria, Australia.
  • O'Brien TJ; School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
  • Kwan P; Department of Neurology, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.
  • Malpas C; Department of Neurology, Alfred Health, Prahran, Victoria, Australia.
  • French JA; Melbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.
BMJ Open ; 14(6): e083929, 2024 Jun 11.
Article em En | MEDLINE | ID: mdl-38862226
ABSTRACT

INTRODUCTION:

This study aims to validate the Seizure-Related Impact Assessment Scale (SERIAS). This novel patient-reported outcome measure (PROM) compares the 'trade-off' between seizures and treatment-related adverse effects, and measures epilepsy disability qualitatively and quantitively. It fills an important gap in PROMs for epilepsy clinical trials and practice. METHODS AND

ANALYSIS:

Adults with epileptologist-confirmed epilepsy from two Australian Epilepsy Centres are being recruited. People with functional seizures, or who are unable to self-complete English-language validated instruments are excluded. Participants providing informed consent are invited to complete questionnaires at baseline, 3 and 6 months later. SERIAS includes five questions that ask about the number of days per month that seizures or treatment-related adverse effects partially or fully impact work/home/school and family/social/non-work activities, as well as a visual analogue scale regarding epilepsy-related disability. SERIAS is completed alongside seven internationally validated instruments measuring treatment-related adverse effects, mood disorders and quality of life. Target recruitment is n=100, ensuring>50 people complete all questionnaires at all timepoints. Comprehensive psychometric analysis will be performed. Convergent validity will be investigated using bivariate correlations with relevant measures. Reliability will be investigated using Cronbach's alpha, McDonald's omega and test-retest correlation coefficients. SERIAS will be a novel PROM for epilepsy clinical trials and practice. ETHICS AND DISSEMINATION Multisite ethics approval was granted by the Alfred Health Ethics Committee (HREC 17/23). Results of this study will be disseminated through publication in peer-reviewed journals and presentations at scientific conferences. TRIAL REGISTRATION NUMBER ACTRN12623000599673.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Psicometria / Qualidade de Vida / Medidas de Resultados Relatados pelo Paciente Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Psicometria / Qualidade de Vida / Medidas de Resultados Relatados pelo Paciente Idioma: En Ano de publicação: 2024 Tipo de documento: Article