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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04595799
Other study ID # 20-AOI-01
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date November 9, 2020
Est. completion date November 9, 2025

Study information

Verified date May 2024
Source Centre Hospitalier Universitaire de Nice
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Multiple sclerosis (MS) is a chronic demyelinating disease of the central nervous system for which the investigators now have many treatment alternatives. These treatments have a preventive goal and the data in the literature suggest the interest in rapidly achieving optimal control of the disease in order to decrease the risk of long-term disability progression. One of the current unmet needs is to have markers that can be used at the individual level to predict the long-term prognosis in order to propose optimal and personalized therapeutic management. Classically used clinical markers do not meet this need. It is recognized that there is a so-called silent course of MS (not measurable by clinical parameters), which may, after several months or years, be expressed as a physical or cognitive disability. MRI is the reference examination for monitoring the sub-clinical activity of the disease but it does not allow the neurodegenerative side of the disease to be assessed. Other blood or imaging markers are being studied but are not yet usable in daily practice. The project aims to evaluate the interest in using digital biomarkers, based on a rapid assessment of patients using a locally developed mobile application (MS Screen Test - MSST) to predict the evolutionary prognosis of the disease.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 240
Est. completion date November 9, 2025
Est. primary completion date November 9, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patient between 18 and 60 years of age - Presenting a diagnosis of relapsing-remitting MS defined according to McDonald 2017 criteria confirmed within 6 months prior to inclusion - Starting first-line treatment (interferon beta, glatiramer acetate, teriflunomide, dimethyl fumarate) - Having an encephalic and cervical MRI in OFSEP format, within 6 months prior to inclusion - No relapse within 30 days prior to inclusion Exclusion Criteria: - presence of a motor, visual or cognitive deficit not related to MS

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Lille University Hospital Lille
France LYON Civil Hospital Lyon
France Montpellier university hospital Montpellier
France Nice University Hospital Nice
France Nimes University Hospital Nîmes
France Paris University Hospital - la pitié salpétriere Paris
France Rennes University Hospital Rennes
France Rouen University hospital Rouen
France Strasbourg University Hospital Strasbourg
France Toulouse university hospital Toulouse

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary speed test in MMST results the average speed (in taps per second or Hz) for the dominant and non-dominant hand 12 months
Primary agility test in MMST results time required (in seconds) to bring the ball to the target as well as the actual time the ball will be held inside the target (expressed as a percentage of the total recording time) 12 months
Primary synchronization test in MMST results the average time interval expressed in milliseconds separating the left and right index strokes. 12 months
Primary visual test in MMST results number of letters seen 12 months
Primary Cognitive test in MMST results the average response latency (the time in milliseconds between the display and the click on a good answer) expressed in milliseconds, the number of wrong answers as well as the number of missed letters.
the average response latency is the combination of multiple measurements (time of response, number of wrong answers and number of missed letters.
12 months
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