Don’t be late! Timely identification of cognitive impairment in people with multiple sclerosis: a study protocol

Author:

Waskowiak Pauline T.,de Jong Brigit A.,Uitdehaag Bernard M. J.,Saddal Shalina R. D.,Aarts Jip,Roovers Aïda A. M.,van Oirschot Pim,de Groot Vincent,Schaafsma Frederieke G.,van der Hiele Karin,Ruitenberg Marit F. L.,Schoonheim Menno M.,Widdershoven Guy A. M.,van der Veen Sabina,Schippers Esther C. F.,Klein Martin,Hulst Hanneke E.,van Munster Casper E. P.,Wieberdink Renske G.,Kragt Jolijn J.,Schouten Judith,Hoogervorst Erwin L. J.,Bouma Paul A. D.,De Kleermaeker Floris G. C. M.,Holleman Meike,Geurts Sofie,de Brabander Christaan,Kalkers Nynke F.,den Teuling Bram A. J.,Vermeer Jos,Schouten Chris C.,Stege Gerard J.,van‘t Hullenaar Thijs,

Abstract

Abstract Background Cognitive impairment occurs in up to 65% of people with multiple sclerosis (PwMS), negatively affecting daily functioning and health-related quality of life. In general, neuropsychological testing is not part of standard MS-care due to insufficient time and trained personnel. Consequently, a baseline assessment of cognitive functioning is often lacking, hampering early identification of cognitive decline and change within a person over time. To assess cognitive functioning in PwMS in a time-efficient manner, a BICAMS-based self-explanatory digital screening tool called the Multiple Screener©, has recently been developed. The aim of the current study is to validate the Multiple Screener© in a representative sample of PwMS in the Netherlands. Additionally, we aim to investigate how cognitive functioning is related to psychological factors, and both work and societal participation. Methods In this cross-sectional multicentre study, 750 PwMS (aged 18–67 years) are included. To obtain a representative sample, PwMS are recruited via 12 hospitals across the Netherlands. They undergo assessment with the Minimal Assessment of Cognitive Functioning in MS (MACFIMS; reference-standard) and the Multiple Screener©. Sensitivity, specificity, and predictive values for identifying (mild) cognitive impairment are determined in a subset of 300 participants. In a second step, the identified cut-off values are tested in an independent subset of at least 150 PwMS. Moreover, test–retest reliability for the Multiple Screener© is determined in 30 PwMS. Information on psychological and work-related factors is assessed with questionnaires. Discussion Validating the Multiple Screener© in PwMS and investigating cognition and its determinants will further facilitate early identification and adequate monitoring of cognitive decline in PwMS.

Funder

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine

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