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NCT07388992Recruiting

Investigating Specific Gait Patterns in Individuals Living With Multiple Sclerosis

Source: ClinicalTrials.gov · Last updated 23 Mar 2026

Brief summary (registry, in English)

The study aims to investigate specific ambulation patterns characteristic of the quality of gait in people with MS (pwMS)

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
28 Jan 2026
Start date
16 Mar 2026
Primary completion date
30 Jun 2026
Lead sponsor
SYSNAV
NCT number
NCT07388992

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 16 Mar 2026 to the primary completion date, 30 Jun 2026
  • 1 site 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.

Prior treatment

  • Participants with a relapse within the past 3 months before the inclusion
  • Past or present pathology other than MS or surgery or trauma impacting gait, ambulatory function or upper limb function, as assessed by the investigator
  • Past or present pathology or surgery or trauma impacting gait, ambulatory function or upper limb function, as assessed by the investigator

Other illness

  • Participants with significant cognitive disorders, limiting the understanding of the exercises to be performed or presence of apparent communication difficulties hindering the correct collection of data, as assessed by the investigator
  • Participants with significant cognitive disorders, limiting the understanding of the exercises to be performed or presence of apparent communication difficulties hindering the correct collection of data, as assessed by the investigator

Other

  • For pwMS:
  • Vulnerable adults: individuals subject to a legal protection measure (guardianship, limited guardianship, or judicial protection) or unable to express their consent.
    • For healthy volunteers (HV):
  • Vulnerable adults: individuals subject to a legal protection measure (guardianship, limited guardianship, or judicial protection) or unable to express their consent.

Who the study is looking for

  • For people living with multiple sclerosis (pwMS):
  • Age at inclusion between =18 and =65 years old
  • Signed informed consent and ability to comply with study and follow-up.
  • Confirmed MS diagnosis according to McDonald criteria (2017)
  • Expanded Disability Status Scale EDSS = 6
  • Stable treatment for 2 months before inclusion (for both disease modifying and symptomatic therapies)
  • Ability and willingness to participate in and comply with all study procedures defined in the protocol
  • Subject will be eligible for enrollment in this study only if either affiliated to, or a beneficiary of a social security category
    • For Healthy volunteers :
  • Age at inclusion between =18 and =65 years old
  • Signed informed consent and ability to comply with study and follow-up.
  • Ability and willingness to participate in and comply with all study procedures defined in the protocol
  • Subject will be eligible for enrollment in this study only if either affiliated to, or a beneficiary of a social security category

Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.