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Resistance Training and Corticospinal Excitability in Multiple Sclerosis

Effects of Supervised Progressive Resistance Training on Central Nervous System Functioning (Corticospinal Excitability) and Walking Capacity in Persons With Multiple Sclerosis

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06374108
Acronym
NEXIMS
Enrollment
54
Registered
2024-04-18
Start date
2024-05-01
Completion date
2026-05-31
Last updated
2024-12-11

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

Conditions

Multiple Sclerosis

Brief summary

The goal of the present study is to investigate effects of progressive resistance training on central nervous system functioning (corticospinal excitability (CSE)) and walking capacity in persons with multiple sclerosis (pwMS). A total of 54 pwMS will be enrolled and randomized into 1 of 3 groups: high dose resistant training (RT), low dose RT, and waitlist control.

Detailed description

Neurodegeneration is a hallmark of multiple sclerosis (MS), affecting both structure and function of the central nervous system (CNS). Neurodegeneration is the main driver of disability progression in MS, evidenced by studies showing deleterious structural and functional CNS changes, ultimately reducing quality of life. Consequently, the interaction between the nervous system and muscular system undergoes deleterious changes causing reduced neuromuscular function (i.e., ability to develop muscle strength and power) and physical function. The functional CNS changes have been evidenced by using the non invasive brain stimulation technique Transcranial Magnetic Stimulation, showing decreased corticospinal excitability alongside increased central motor conduction time. Moreover, functional peripheral nervous system (PNS) changes have been evidenced by nerve conduction methods, revealing decreased amplitude of compound muscle action potential and increased latency of nerve signaling. In an ongoing exploratory study (unpublished), the investigators have observed that functional CNS and PNS outcomes deteriorate with disability progression from healthy to mildly to moderately disabled people with MS (PwMS). Exercise is beneficial from both an individual and a societal perspective, and has proven to be both safe and without any noticeable side effects in PwMS. Resistance training (RT) appears particularly effective in improving neuromuscular function (mainly muscle strength) and physical function (especially walking capacity). Whilst RT and other exercise modalities may elicit positive effects on CNS structure in PwMS, it seems to require a long-term (≥ 6 months) exposure. In contrast, CNS (and potentially PNS) function may adapt much more rapidly, despite a scarcity of studies (and with heterogeneous findings) involving PwMS. Interestingly, an exploratory exercise study (non-controlled, low sample size, 10 weeks treadmill walking intervention) assessed corticospinal excitability in PwMS, and observed substantial improvements after the intervention. Apart from this study, a major knowledge gap exists in terms of elucidating the potential beneficial effects of exercise (RT in particular) on CNS (and PNS) function. Based on evidence from healthy young individuals, substantial improvements in corticospinal excitability have been shown following 2-12 weeks of RT, supporting that RT-induced improvements in corticospinal excitability can also be seen in PwMS. Lastly, as existing exercise guidelines for PwMS fails to refer to evidence on dose-response to exercise, and a recent systematic review on exercise studies found no dose-response studies in PwMS (n=202), this aspect is also of great clinical relevance.

Interventions

BEHAVIORALProgressive resistance training

The RT exercise regime will focus on lower extremity exercises (60-90% of 1 repetition maximum) as well as incorporating functional exercises.

Sponsors

University of Aarhus
Lead SponsorOTHER
Aarhus University Hospital
CollaboratorOTHER
University of Copenhagen
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * MS diagnosis according to the McDonald diagnostic criteria * Shows impairments in walking capacity * Ability to self transport to test and exercise

Exclusion criteria

* Pregnancy * Neurological or other comorbidities that affects the nervous system * Relapse within the past 2 months * Pacemaker or metallic implants * Hypertension (medically unregulated) * Participation in structured RT over the past 3 months (≥ 2 sessions/week).

Design outcomes

Primary

MeasureTime frameDescription
MEP/Mmax ratioChange from Baseline to 10 weeksCortical excitability measured as amplitude percentage ratio between MEP (resting) and Mmax (Cmap of TA). Unit (intended): %

Secondary

MeasureTime frameDescription
Voluntary activation IChange from Baseline to 10 weeksAssessed by Interpolated Twitch Technique (ITT) (dorsal flexion). Unit (intended): %
Voluntary activation IIChange from Baseline to 10 weeksEMG amplitude during MVC (plantar flexion and dorsal flexion). Unit (intended): μV
Force SteadinessChange from Baseline to 10 weeksA quantitative measure of the ability to control muscle tonus (dorsal flexion). Unit (intended): root-mean-square (RMS) error (Coefficient of Variation (CV))
Rate of Force DevelopementChange from Baseline to 10 weeksThis is defined as the speed at which the contractile elements of the muscle can develop force (plantar flexion and dorsal flexion). Unit (intended): N/s
UltrasoundChange from Baseline to 10 weeksMeasure of muscle thickness of the tibialis anterior. Unit (intended): mm
Resting Motor Threshold (rMT)Change from Baseline to 10 weeksThe intensity necessary to produce a motor-evoked potential (MEP) that exceeds a defined peak-to-peak amplitude (50 μV) 50% of the time in a finite number of trials. Unit (intended): % Maximum stimulator output (MSO)
Active Motor Threshold (aMT)Change from Baseline to 10 weeksThe intensity necessary to produce a motor-evoked potential (MEP) that exceeds a defined peak-to-peak amplitude (50 μV) 50% of the time in a finite number of trials during voluntary activation (20% of MVC). Unit (intended): % Maximum stimulator output (MSO)
MEP latency (resting)Change from Baseline to 10 weeksThe transmission time from stimulating the cortex to the start of the evoked potential in the EMG of the target muscle. Unit (intended): ms
MEP latency (active)Change from Baseline to 10 weeksThe transmission time from stimulating the cortex to the start of the evoked potential in the EMG of the target muscle. Unit (intended): ms
MEP amplitude (resting)Change from Baseline to 10 weeksPeak-to-peak of averaged MEP (20 stimulations of 120% rMT). Unit (intended): mV
MEP amplitude (active)Change from Baseline to 10 weeksPeak-to-peak of averaged MEP (20 stimulations of 120% rMT). Unit (intended): mV
Short-interval intracortical Inhibition (SICI)Change from Baseline to 10 weeksSICI measures cortical inhibition and is a TMS protocol in which two stimuli are delivered with an interstimulus interval (ISI) of 2.5 ms. Unit (intended): the relative amplitude difference of motor evoked potentials (MEPs) (%).
Intracortical facilitation (ICF)Change from Baseline to 10 weeksICF measures cortical facilitation and is a TMS protocol in which two stimuli are delivered with an interstimulus interval (ISI) of 10 ms. Unit (intended): the relative amplitude reduction of motor evoked potentials (MEPs) (%).
Cortical Silent Period (CSP)Change from Baseline to 10 weeksThe temporary interruption of electromyographic signal from a muscle following a motor-evoked potential (MEP) triggered by transcranial magnetic stimulation (TMS). Unit (intended): ms
Central Motor Conduction Time (CMCT)Change from Baseline to 10 weeksThe time it takes for the fastest action potentials to travel from the site of cortical stimulation to the spinal motoneuron. It is calculated by subtracting the peripheral motor conduction time (PMCT) from the MEP latency or by the F-wave method. Unit (intended): ms
Muscle strengthChange from Baseline to 10 weeksMaximal voluntary contraction (MVC) is the maximal force-generating capacity (plantar flexion and dorsal flexion). Unit (intended): N
Timed 25 feet walk test (T25FWT)Change from Baseline to 10 weeksObjective test that measures walking speed. Unit (intended): seconds.
6-minute walk test (6MWT)Change from Baseline to 10 weeksObjective test that measures walking endurance. Unit (intended): meters.
Six spot step test (SSST)Change from Baseline to 10 weeksObjective test that measures walking coordination and balance. Unit (intended): seconds.
5 sit-to-stand (5STS)Change from Baseline to 10 weeksObjective test that measures functional lower limb muscle strength and power. Unit (intended): seconds.
9-step stair ascend (9SSA)Change from Baseline to 10 weeksObjective test that measures functional lower limb muscle strength and power. Unit (intended): seconds.
Patient determined disease steps (PDDS)Change from Baseline to 10 weeksA patient-reported measure of disability. Unit (intended): score (0-8; 0 is normal).
Multiple Sclerosis Walking Scale (MSWS)Change from Baseline to 10 weeksQuestionnaire that measures quality of life. Unit (intended): score (0-100; 0 is better).
Modified fatigue impact scale (MFIS)Change from Baseline to 10 weeksQuestionnaire that measures the impact fatigue has on daily life. Unit (intended): score (0-84; 0 is better)
MS impact scale (MSIS)Change from Baseline to 10 weeksQuestionnaire that measures the impact MS has on daily life. Unit (intended): score (29-145; 29 is better)
Falls-efficacy scale - international (FES-1)Change from Baseline to 10 weeksQuestionnaire that measures concerns about falling. Unit (intended): score (16-64; 16 is better)
The Physical Activity Enjoyment Scale (PACES)Change from Baseline to 10 weeksQuestionnaire that measures enjoyment for physical activity. Unit (intended): score (8-56; Higher score reflect greater level of enjoyment)
Brief pain inventory (BPI)Change from Baseline to 10 weeksQuestionnaire that measures pain severity and pain interference. Unit (intended): No scoring algorithm, but worst pain or the arithmetic mean of the four severity items can be used as measures of pain severity; the arithmetic mean of the seven interference items can be used as a measure of pain interference.
Baecke physical activityChange from Baseline to 10 weeksQuestionnaire (patient-reported outcome) assessing patient-reported participation in physical activities. Unit (intended): Score range is continuous (0-xx). Higher is better.
AccelerometryChange from Baseline to 10 weeksMethod used to measures and analyze movement and acceleration in three dimensions of a person (physical activity). Unit (intended): g (m/s\^2)
EEG-EMG coherence (0-1)Change from Baseline to 10 weeksSynchronization between brain activity (EEG) and muscle activity (EMG) over a specific frequency range. Unit (intended): ranging from 0 to 1, where 0 is no coherence and 1 is perfect coherence.

Countries

Denmark

Contacts

Primary ContactLars Hvid, PhD
lhvid@ph.au.dk93508717

Outcome results

None listed

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