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Clinical Trials/NCT04837365
NCT04837365CompletedNot Applicable

Impact of Neuropsychological Disorders on Visual Exploration, Walking Initiation and Walking in Multiple Sclerosis

Lille Catholic University3 sites in 1 country32 target enrollmentStarted: May 21, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
32
Locations
3
Primary Endpoint
Cadence of walking (in cycles.min-1)

Study Overview

Brief Summary

The study involves MS patients with and without neuropsychological disorders.

The patient will benefit from:

  • A routine neuropsychological assessment, including a cognitive and emotional assessment
  • A clinical examination
  • A three-dimensional analysis of movement

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Understanding and able to speak French
  • Carriers of MS with relapsing remitting form (RRMS-RR) with an EDSS <4
  • No significant motor, cerebellar or somesthesia disorders of the upper limbs or visual disturbances (side to a visual EDSS <2)
  • Absence of corticosteroid intake in the last four weeks
  • Benefiting from health insurance coverage
  • Not showing any flare-ups or worsening of the disease in the last 6 weeks
  • No botulinum toxin injection for more than 4 months

Exclusion Criteria

  • People with previous neurological pathologies, head trauma with loss of consciousness, psychiatric pathologies, serious general ailments, perceptual or dysarthric disorders preventing verbal communication or reading,
  • Treatment with psychotropic drugs (except benzodiazepines and hypnotics).
  • Refusal to participate after clear and fair information about the study.
  • Adults under tutorship, curatorship or safeguard of justice
  • With orthopedic treatment influencing walking
  • Pregnant woman

Arms & Interventions

patients without neuropsychological disorders

Other

Intervention: Three dimensional gait analysis with eyetracking (Other)

patients with neuropsychological disorders

Other

Intervention: Three dimensional gait analysis with eyetracking (Other)

Outcomes

Primary Outcomes

Cadence of walking (in cycles.min-1)

Time Frame: 60 days

The kinematics of the initiation of walking and walking will be appreciated thanks to the variables calculated at the level of the joints of the lower limbs as well as the spatio-temporal parameters without and with management of obstacles (taking a step, balloon)

Range of motion in the lower limbs in degrees

Time Frame: 60 days

The kinematics of the initiation of walking and walking will be appreciated thanks to the variables calculated at the level of the joints of the lower limbs as well as the spatio-temporal parameters without and with management of obstacles (taking a step, balloon)

Step length (in m)

Time Frame: 60 days

The kinematics of the initiation of walking and walking will be appreciated thanks to the variables calculated at the level of the joints of the lower limbs as well as the spatio-temporal parameters without and with management of obstacles (taking a step, balloon)

Walking speed (in m.s-1)

Time Frame: 60 days

The kinematics of the initiation of walking and walking will be appreciated thanks to the variables calculated at the level of the joints of the lower limbs as well as the spatio-temporal parameters without and with management of obstacles (taking a step, balloon)

Secondary Outcomes

  • Ocular fixation time (measured in ms)(60 days)
  • Displacements (in mm) during walking(60 days)
  • Muscle contractions determined by the electromyogram (EMG) (mV)(60 days)
  • Acceleration (in mm.s-2) during walking(60 days)
  • Joint angles(60 days)

Investigators

Sponsor
Lille Catholic University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (3)

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