Eccentric Cycling in Multiple Sclerosis Rehabilitation
Eccentric Cycling : a New Training Modality in Multiple Sclerosis Rehabilitation
1 other identifier
interventional
60
1 country
1
Brief Summary
The project aims to optimise functional rehabilitation programmes for people with multiple sclerosis. Investigators are proposing eccentric cycling as a new exercise modality for treating these patients. Based on previous results in healthy subjects, investigators will attempt to define the optimal parameters of this new modality (in terms of duration, intensity, frequency, etc.). Investigators also aim to demonstrate the effectiveness of this training (compared to conventional training) in improving muscle function, functional capacity, perception of chronic fatigue, quality of life, physical condition, and neurological and cognitive function.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable multiple-sclerosis
Started Jan 2026
Shorter than P25 for not_applicable multiple-sclerosis
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 8, 2025
CompletedStudy Start
First participant enrolled
January 1, 2026
CompletedFirst Posted
Study publicly available on registry
January 5, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
January 5, 2026
December 1, 2025
9 months
December 8, 2025
December 23, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Maximal Isometric Force
Maximal Isometric Force (in Newton-meters - Nm) of the quadriceps will be measured using a fixed dynamometer (Kinvent), at 90 degrees of knee flexion.
At baseline and endline of intervention (Week 1 and 14)
Walking distance
6 minutes walking test and 2 minutes walking test will be performed to measure the walking capacities (in meters) of participants.
At baseline and endline of intervention (Week 1 and 14)
Secondary Outcomes (11)
Handgrip strength
At baseline and endline of intervention (Week 1 and 14)
Spasticity
At baseline and endline of intervention (Week 1 and 14)
Timed up and go
At baseline and endline of intervention (Week 1 and 14)
Neurocognitive capacity
At baseline and endline of intervention (Week 1 and 14)
Berg Balance Scale
At baseline and endline of intervention (Week 1 and 14)
- +6 more secondary outcomes
Other Outcomes (8)
Height
At baseline and endline of intervention (Week 1 and 14)
Weight
At baseline and endline of intervention (Week 1 and 14)
Body fat percentage
At baseline and endline of intervention (Week 1 and 14)
- +5 more other outcomes
Study Arms (2)
Eccentric group
EXPERIMENTALConcentric group
ACTIVE COMPARATORInterventions
Eligibility Criteria
You may qualify if:
- Diagnosis of multiple sclerosis
- Multiple sclerosis: EDSS score \< 7
- Age under 75 years
- Stable disease state
- Written medical clearance authorizing participation
- Legal adult status
- Written informed consent, with demonstrated understanding of the consent form (via a few specific questions)
- Ability to mobilize independently (e.g., transfers, walking)
You may not qualify if:
- One or more contraindications to physical activity
- Significant comorbidities
- Current hospitalization or undergoing changes in medication
- Active flare-up
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Liegelead
- University Hospital Sart Tilman, Liegecollaborator
Study Sites (1)
Liege University
Liège, Liège, 4000, Belgium
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Stéphanie HODY, PhD
Department of Physical Activity and Rehabilitation Sciences, University of Liege and University Hospital of Liege, Liege, Belgium
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physiotherapist
Study Record Dates
First Submitted
December 8, 2025
First Posted
January 5, 2026
Study Start
January 1, 2026
Primary Completion (Estimated)
October 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
January 5, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share