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Multiparametric Assessment to Investigate Prognostic Factors for Disease Evolution a nd Evolutionary Patterns of Cognitive Status in RRMS

Multiparametric Clinical, Radiological, Neuropsychological, and Neurophysiological Assessment to Investigate Prognostic Factors for Disease Evolution and Treatment Response in MS: a Prospective Study.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05510817
Acronym
COGNIT-MS
Enrollment
50
Registered
2022-08-22
Start date
2022-06-06
Completion date
2026-06-06
Last updated
2023-12-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis, Relapsing-Remitting

Keywords

MRI, evoked potentials, cognitive function, PROMs

Brief summary

This prospective study combining non conventional MRI techniques, neuropsychological screening tools, and a neurophysiological work-up using a sensitive and validated battery, will evaluate the predictive value of these measures and will explore the changes of the cognitive scores from baseline.

Detailed description

Neurologists are in need for reliable and robust predictive factors enabling to predict disease evolution and treatment response. Moreover, recent studies suggested that the evolution patterns of cognitive status in MS could be mixed, contradicting the concept that cognitive impairment in MS will inevitably increase over time. The main aim of this prospective study is to investigate the predictors of disease evolution, as measured by the EDSS score, using a multiparametric assessment combining neuropsychological tests (BCcogSEP battery), MRI-derived metrics (volumetric brain parameters, tractography, diffusion tensor imaging and fiber tracking), patient-reported outcome measures, and neurophysiological tools (multimodal evoked potentials), and to explore the evolutionary patterns of cognitive status (changes from baseline). The investigators planned to include 50 patients with active RRMS and initiating a new disease-modifying treatment. Yearly assessment starting from study inclusion will be performed.

Interventions

OTHERMultiparametric assessment

neuropsychological assessment, PRO measures, non-conventional MRI metrics

Sponsors

Saint-Luc University Hospital
CollaboratorUNKNOWN
University Hospital of Mont-Godinne
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* active MS, according to the Lublin criteria * disease duration \< 10 years before initiating or changing a disease-modifying therapies, * relapse- and steroid-free for at least 1 month before MRI acquisition * between 18-50 years old * having given informed consent * with no significant comorbidity other than MS or substance abuse that could interfere with cognitive performances

Exclusion criteria

* progressive forms of MS

Design outcomes

Primary

MeasureTime frameDescription
Predictors of disease evolution3 yearsEDSS score worsening from baseline
evaluation of evolutionary patterns of cognitive status (impaired vs non impaired)/changes from baseline3 yearschanges from baseline in cognitive scores
baseline predictors of future cognitive impairment3 yearsabnormal cognitive performances based on cognitive scores (using BCcogSEP battery)

Secondary

MeasureTime frameDescription
alteration in strategic white matter tracts at the early stages of RRMS, in patients with and without cognitive impairment3 yearsfractional anisotropy
predictive role of mEPS in predicting future disability3 yearsthe Global Evoked Potential (GEP) score at study entry (baseline); EDSS score changes from baseline

Countries

Belgium

Contacts

Primary ContactFrédéric London, MD
frederic.london@chuuclnamur.uclouvain.be+3282413345

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026