Impact of Exercise Training on Serum Neurofilament Light Chain (NfL), Brain Volumetry, and Functional Outcomes in Multiple Sclerosis
What it found
No result yet.
What was tested
Treatment tested
- Exercise
What it measured
Main measures
MRI Acquisition and Volumetric Analysis
12 weeks
MRI lesionsSerum Neurofilament Light Chain (NfL) measurement
12 Weeks
Blood or spinal fluid markers
Other measures (5)
Multiple Sclerosis Functional Composite
12 Weeks
Disability progressionFatigue Impact Scale
12 Weeks
FatigueShort form-12 version 2 (SF-12v2)
12 Weeks
PainQuality of life (reported by participants)Problem-Solving inventory (PSI)
12 Weeks
Bladder, bowel and sexual functionEmotional intelligence scale (EIS)
12 Weeks
Who could take part
Relapsing MS · 18 to 65
Inclusion Criteria: * Clinically confirmed relapsing-remitting multiple sclerosis (RRMS) diagnosis according to revised McDonald criteria (2017) * Mild-to-moderate disability (EDSS score 1.0-5.5) * No corticosteroid treatment within the previous 3 months Exclusion Criteria: * Acute MS relapse within 90 days prior to enrollment * Regular participation in structured exercise programs (>3 hours/week) * Comorbid conditions that may limit exercise participation, including; significant orthopedic impairments, unstable cardiopulmonary conditions and other systemic disorders affecting physical activity * Standard MRI contraindications (metallic implants, claustrophobia, etc.) * Concurrent neurological disorders (other than MS) * Initiation or modification of disease-modifying therapy within 6 months * Severe spasticity (Modified Ashworth Scale ≥3 in any major muscle group)
As registered. Criteria can change, so ask the trial team or your neurologist.
Contact details on the registryAbout this trial
In the sponsor's words
This single-blind, randomized controlled trial will employ a two-arm parallel design (exercise group vs. control group) with a 12-week intervention period. Randomization will be implemented using SPSS 25.0 (IBM Corporation, Armonk, NY, USA) to ensure balanced group allocation. All outcome measures will be assessed at baseline and post-intervention.
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History
Started
Apr 2026
Main results due
Apr 2026
Finished
Aug 2026
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