Clinical Trials in France / NCT05482906
Recruiting
Observational
Common and Specific Information From Neuroimaging and Smartphone
NCT05482906 · tracked via the Priya Life Science France tracker
Condition(s) studied
Multiple Sclerosis
Investigational drug(s) / intervention(s)
eGait
eGait: IMU sensor (as part of eGait device) worn at the hip during T25FW
Study summary
Gait alteration is frequent in MS and limitation in walking ability is a major concern in MS patients. Umanit and LMJL (Nantes university) has developed a device call egait to assess walking ability in individuals (eg MS patients).
Eligibility
Inclusion Criteria :
* Diagnosis of MS based on McDonald criteria (including Relapsing-remitting and progressive MS)
* Over 18 years old /age greater than 18 years
* Patients followed at Nantes university hospital or Rennes university hospital
* Last known EDSS before inclusion ranging from 0 to 6 inclusive/EDSS of 0 to 6 inclusive, prior inclusion
* No relapse within 3 months
* With a Medullar MRI planed as part as usual care
* MRI scan can be performed within a maximum of 4 months after or before the walking test.
* Affiliated person or beneficiary of a social security scheme
Exclusion Criteria :
* Bilateral aid needed to walk
* Women who are pregnant
* Patient having expressed their opposition
* Patient under guardianship or security measure
Primary outcome measure(s)
- Clustering analyze based on IGP — At the inclusion
IGP consists of a curve, based on quaternion and representing the rotation recorded by the IMU during an average gait cycle (0-1). - Clustering analyze based on EDSS score — At the inclusion
EDSS is an ordinal scale measuring disability and ranging from 0 (normal examination) to 10 (death due to MS) in a 0,5-point increments from score 1. - Clustering analyze based on MRI lesion load — At the inclusion
MRI characteristics are spinal and extraspinal lesion volumes.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Nantes University Hospital | Nantes | Loire-Atlantique | Recruiting |
More Nantes University Hospital trials in France
Other trials for the same condition
Grey Matter Damage at the Earliest Phase of Multiple Sclerosis : a Longitudinal 7T MRI Study
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A Study to Evaluate the Efficacy, Safety and Pharmacokinetics (PK) of a Higher Dose of Ocrelizumab in Adults With Primary Progressive Multiple Sclerosis (PPMS)
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Safety and Efficacy of Fingolimod in Pediatric Patients With Multiple Sclerosis
Active, not recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05482906 on ClinicalTrials.gov ↗ ← All trials in France