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Multiple Sclerosis Performance Test: Technical Development and Usability

Authors :
Wendy Gabel
Christine Reece
Stephen M. Rao
Jane Rhodes
David Schindler
Glenn Phillips
Colleen C. Mullen
Ellen M. Mowry
Lauren Krupp
Richard A. Rudick
Deborah M. Miller
Fernando Venegas
Jaime L. Freiburger
Francois Bethoux
Robert A. Bermel
James Williams
Jay L. Alberts
Lyla Mourany
Efrosini T. Bruzik
Source :
Advances in Therapy
Publication Year :
2019
Publisher :
Springer Science and Business Media LLC, 2019.

Abstract

Introduction In the clinic, the assessment of patients with multiple sclerosis (MS) is typically qualitative and non-standardized. Objectives To describe the MS Performance Test (MSPT), an iPad Air® 2 (Apple, Cupertino, CA, USA)-based neurological assessment platform allowing patients to input relevant information without the aid of a medical technician, creating a longitudinal, clinically meaningful, digital medical record. To report results from human factor (HF) and usability studies, and the initial large-scale implementation in a practice setting. Methods The HF study examined use-error patterns in small groups of MS patients and healthy controls (n = 14), the usability study assessed the effectiveness of patient interaction with the tool by patients with a range of MS disability (n = 60) in a clinical setting, and the implementation study deployed the MSPT across a diverse population of patients (n = 1000) in a large MS center for routine clinical care. Results MSPT assessments were completed by all users in the HF study; minor changes to design were recommended. In the usability study, 73% of patients with MS completed the MSPT, with an average administration time of 32 min; 85% described their experience with the tool as satisfactory. In the initial implementation for routine care, 84% of patients with MS completed the MSPT, with an average administration time of 28 min. Conclusion Patients with MS with varying disability levels completed the MSPT with minimal or no supervision, resulting in comprehensive, efficient, standardized, quantitative, clinically meaningful data collection as part of routine medical care, thus allowing for large-scale, real-world evidence generation. Funding Biogen. Trial Registration NCT02664324. Electronic supplementary material The online version of this article (10.1007/s12325-019-00958-x) contains supplementary material, which is available to authorized users.

Details

ISSN :
18658652 and 0741238X
Volume :
36
Database :
OpenAIRE
Journal :
Advances in Therapy
Accession number :
edsair.doi.dedup.....0eec505aa430695f257d4b6f5e602da6
Full Text :
https://doi.org/10.1007/s12325-019-00958-x