NCT06634225Completed
Use of Inertial Units in Patient With Multiple Sclerosis (IMUSEP)
IMUSEP : Use of Inertial Navigation Systems to Detect and Characterize Early Locomotor Disorders in Patients With Multiple Sclerosis.
Source: ClinicalTrials.gov · Last updated 12 Mar 2026
Brief summary (registry, in English)
The goal of this case control study is to evaluate the use of inertial navigation systems to detect and characterize early locomotor disorders in patients with multiple sclerosis (MS). The study aims to: • Validate the contribution and inefficiency indexes obtained by the Trigno® Avanti Sensor inertial units, in comparison with indexes calculated with 3D motion analysis during walking and tandem in early-stage MS patients. Researchers will compare MS patients, to healthy controls.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 70 (actual)
- First submitted
- 7 Oct 2024
- Start date
- 8 Nov 2024
- Primary completion date
- 19 Dec 2025
- Lead sponsor
- Lille Catholic University
- Diseases
- Multiple sclerosis
- NCT number
- NCT06634225
What you commit to
- Study type: Observational
- Participants enrolled: 70
- From 8 Nov 2024 to the primary completion date, 19 Dec 2025
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Unstable cardiac and respiratory pathology
- Patients with comprehension or cognitive disorders
- Allergy to silver
- Allergy to silver
Other
- MS crisis within the last 6 weeks
- Botulinum toxin injection in the last 3 months
- Neurological pathology other than MS
- Disabling musculoskeletal pathology
- Pregnant women
- Recent change in background treatment (\< 3 months)
- Patients under guardianship or curatorship
- Presence of implanted electronic devices of any kind, including pacemakers or similar assistive devices, electronic infusion pumps and implanted pacemakers
- Neurological pathology
- Rheumatological pathology
- Antecedent of sprains (\< 3 months), fractures (\< 1 year) in the lower limbs
- Pregnant women
- Person under guardianship or trusteeship
- Presence of implanted electronic devices of any kind, including pacemakers or similar assistive devices electronic infusion pumps and implanted pacemakers
Who the study is looking for
- Age 18 to 65 (inclusive)
- Expanded Disability Status Scale (EDSS) ≤ 4
- Proficient in French
- Agreeing to participate in the study and having signed the informed consent form
- Affiliated with a social security scheme
- Age 18 to 65 (inclusive)
- Proficient in French
- Agreeing to participate in the study and having signed the informed consent form
- Affiliated with a social security plan
Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Saint-Philibert hospital Coordinator of this site? Confirm its status | Lomme | France | Unknown status |
| Saint-Amand-Les-Eaux Hospital Coordinator of this site? Confirm its status | Saint-Amand-les-Eaux | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.