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Effects of Ten-Weeks Progressive Resistance Training on Neuromuscular Performance, Mobility, Heart Rate Variability and Sleep Quality in Persons With Multiple Sclerosis

Effects of Ten-Weeks Progressive Resistance Training on Neuromuscular Performance, Mobility, Heart Rate Variability and Sleep Quality in Persons With Multiple Sclerosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04452760
Enrollment
36
Registered
2020-06-30
Start date
2020-07-15
Completion date
2020-10-05
Last updated
2020-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Keywords

neurological disorders, resistance training, strength training, sleep quality, neuromuscular performance, functional capacity

Brief summary

Multiple Sclerosis (ME) is a degenerative, inflammatory and autoimmune demyelinating disease of the central nervous system, characterized by demyelination due to inflammation and degeneration of the myelin sheaths enveloping nerves of the eye, periventricular grey matter, brain, spinal cord and brainstem. The symptoms associated with MS include symptomatic fatigue, muscle weakness, ataxia, mobility and balance problems or cognitive problems. Strength training has been shown to improve strength and mobility in persons with MS.

Detailed description

Multiple Sclerosis (ME) is a degenerative, inflammatory and autoimmune demyelinating disease of the central nervous system, characterized by demyelination due to inflammation and degeneration of the myelin sheaths enveloping nerves of the eye, periventricular grey matter, brain, spinal cord and brainstem. The symptoms associated with MS include symptomatic fatigue, muscle weakness, ataxia, mobility and balance problems or cognitive problems. Resistance training has been shown to improve strength, sleep quality and mobility in persons with MS.

Interventions

OTHERPhysical exercise

Physical exercise intervention

Testing sessions

Sponsors

Universidad Católica San Antonio de Murcia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* mild or moderate disability with clinical mild spastic-ataxic gait disorder. * stable phase of the disease.

Exclusion criteria

* Expanded Disability Status Scale (EDSS) \< 6. * relapsing disease within the preceding 12 months. * corticosteroid treatment within the last months before study inclusion.

Design outcomes

Primary

MeasureTime frameDescription
Maximal Voluntary Isometric Contraction of Knee ExtensionBefore the program trainingthe maximum force (N) that can be produced voluntarily by the knee extension muscles during an isometric contraction is measured. The leg of the participant is fixed to an isokinetic device, and the participant makes a 5-second attempt, developing all the strength he or she can.
Rate of Force DevelopmentBefore the program trainingRate of force development in knee extension
Central Activation RatioBefore the program trainingThe central activation ratio (CAR) was determined using superimposed electrical stimulation during maximum voluntary contractions
SpasticityBefore the program trainingPendulum test

Secondary

MeasureTime frameDescription
Walking speedBefore the program trainingTest 10 m-walks
Sleep QualityBefore the program trainingAcelerometry and Karolinska Sleep Diary
Static BalanceBefore the program trainingRomberg Test with eyes open and closed. Analysis with force plates
Functional capacityBefore the program trainingSit-to-Stand Test
Heart Rate VariabilityBefore the program trainingSleeping Heart Rate Variability

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026