TofCoMS: The Effect of Covid-19 on the Disease Course of Multiple Sclerosis :Belgian Lessons Learned From Rocky I to Rocky IV

Sponsor
Marie D'hooghe (Other)
Overall Status
Completed
CT.gov ID
NCT05403463
Collaborator
(none)
230
1
3
76.1

Study Details

Study Description

Brief Summary

Retrospective observational cohort study. ToFCoMS: two years of follow-up of COVID-19 in MS.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Methods The Nationaal Multiple Sclerose Centrum (NMSC) Melsbroek is a large highly-specialized center specifically focusing on neurological management, multidisciplinary care and rehabilitation in patients with MS. Since March 2020 (i.e., the onset of the pandemic in Belgium, and the first of five waves of spiking infection numbers thus far in our country), clinical data of patients followed at the center have been collected in a local database in case of COVID-19 diagnosis. The following items have been recorded: name, gender and date of COVID-19 diagnosis; age, Expanded Disability Status Scale score, MS duration, clinical subtype and DMT regimen at time of COVID-19 diagnosis; COVID-19 severity (method 1: categorized as ambulatory, hospitalized, death; method 2: categorized as asymptomatic, mild illness, moderate illness, severe illness, critical illness and death); vaccination status (categorized as non-vaccinated, fully vaccinated, fully vaccinated + booster) at time of COVID-19 diagnosis. On February 28, 2022, this database was locked and consisted of 234180 unique individual COVID-19 cases.

    The NMSC Melsbroek features a second and more large database containing a broad variety of (para)clinical information gathered during routine follow-up, which includes regular testing of general disability with the EDSS, leg function/ambulation with the Timed 25-Foot Walk Test (T25FWT), hand function/dexterity using the 9-Hole Peg Test (9HPT) and cognition/information processing speed with the Symbol Digit Modalities Test (SDMT). For each of these parameters, the first two assessments before COVID-19 diagnosis (labelled T0 and T1, respectively; T1 is the closest to COVID-19 diagnosis), and the first thereafter (labelled T2), were retrieved for each COVID-19 subject. If clinical measurements were performed during an in-house stay for rehabilitation purposes, only those performed on admission were retained (thus not necessarily those the closest to the COVID-19 infection).

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    230 participants
    Observational Model:
    Other
    Time Perspective:
    Retrospective
    Official Title:
    The Effect of Covid-19 on the Disease Course of Multiple Sclerosis
    Actual Study Start Date :
    Mar 1, 2022
    Actual Primary Completion Date :
    Jun 1, 2022
    Actual Study Completion Date :
    Jun 1, 2022

    Outcome Measures

    Primary Outcome Measures

    1. The investigators hereby aim to answer the question whether COVID-19 affects the progression of clinical disability in MS [2 years]

      The difference between the values measured at T-2 and T-1 (i.e., before COVID-19) will be compared, after adjustment for the time interval, with the difference between the respective values measured at T-1 and T1 (i.e., after COVID-19) for T25WT, 9HPT and SDMT. The investigators hereby aim to answer the question whether COVID-19 affects the progression of clinical disability in MS. Its effect on SDMT evolution has been defined as the primary endpoint of our study.

    Secondary Outcome Measures

    1. vaccination status and progression MS [2 years]

      As secondary outcomes, the investigators want to explore whether (a) there is a relationship between COVID-19 severity and the evolution of clinical disability (i.e., differences between T-1 and T1), (b) vaccination status affects COVID-19 severity (in the total cohort as well as stratified according to DMT) and evolution of clinical disability (i.e., differences between T-1 and T1) and (c) DMT influences COVID-19 severity and evolution of clinical disability (i.e., differences between T-1 and T1).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    diagnosis of Multiple Sclerosis Covid 19 infection with PCR test

    Exclusion Criteria:

    other diagnosis than Multiple Sclerosis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Nationaal MS center Melsbroek Vlaams Brabant Belgium 1820

    Sponsors and Collaborators

    • Marie D'hooghe

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Marie D'hooghe, neuroloog, National MS Center Melsbroek
    ClinicalTrials.gov Identifier:
    NCT05403463
    Other Study ID Numbers:
    • TofComs
    First Posted:
    Jun 3, 2022
    Last Update Posted:
    Jun 8, 2022
    Last Verified:
    Jun 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 8, 2022