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Resistance Training and Nerve Signals in Multiple Sclerosis

Tests strength training effects on nerve signals and walking in adults with multiple sclerosis.

Plain-language title generated from the registry record
Registry title: Resistance Training and Corticospinal Excitability in Multiple Sclerosis

Key facts

Where
Aarhus and Copenhagen, DenmarkSee the 2 sites

Where in Denmark

  • Department of Public HealthAarhus, DenmarkTaking people
  • Department of Nutrition, Exercise and Sports, University of CopenhagenCopenhagen, DenmarkTaking people

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Trial details

Who runs it
University of Aarhus
Trial code
NCT06374108
Record updated
11 December 2024
Original description
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.Read full original descriptionShow less

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

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.

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

ClinicalTrials.gov NCT06374108