Menu
Recruiting NCT06219304

Effect of High Intensity Training on Motor and Cognitive Functions

No phase Interventional Multiple Sclerosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Multimodal functional training, Usual care.
Who it may be relevant to
Registry conditions: Multiple Sclerosis. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluation of the Impact of Experimentally Induced Fatigability on Motor and Cognitive Functions. Effect of High Intensity Training on Motor and Cognitive Functions:a Pilot Randomized Controlled Trial

Overview

Fatigability is one of the most prevalent disorder in MS followed by walking, balance and cognitive disorders. However, there are few experimental studies on the effects of fatigability on balance and gait hampering the knowledge of causal fatigue-related changes of walking, balance and cognition. Nowadays, instrumented systems such as wearable devices and optoelectronic systems are available and can be used to provide quantitative and objective indexes useful to monitor the changes of gait parameters during a fatiguing performance. (Moreover), instrumented assessment of patients' performances in dual task paradigms can reveal the possible impact of fatigability on cognitive functions. So far, high intensity functional training has been already used in MS to reduce fatigability. However, the true impact of reduced fatigability on walking, balance and cognition has not been assessed after a fatiguing task making impossible to understand the real impact of treatments focusing on fatigability on these functions. Thus, the aims of the present proposal are to assess the: 1) the acute effect of experimentally induced motor fatigability on walking, balance and cognitive functions using an objective instrumented assessment before, during, and after an overground fatiguing walking test. 2) to investigate the effect of high intensity multimodal functional training to improve motor and cognitive disorders.

Interventions

  • Other Multimodal functional training
    40 minutes of multimodal functional training: 20 minutes of aerobic training on treadmill, 10 minutes of dynamic balance training; 10 minutes of functional strength training.
  • Other Usual care
    Exercises aimed at improving balance and mobility

Primary outcome measures

  • difference in walking velocity during the fatiguing walking test [Time frame: Baseline and at 6-8 weeks (after the completion of 16 training sessions)]
Secondary outcome measures (3)
  • gait asymmetry and gait regularity [Time frame: Baseline and at 6-8 weeks (after the completion of 16 training sessions)]
  • Antero-posterior and medio-lateral accelerations in stabilometric tasks [Time frame: Baseline and at 6-8 weeks (after the completion of 16 training sessions)]
  • Brief International Cognitive Assessment in Multiple Sclerosis (BICAMS) [Time frame: Baseline and at 6-8 weeks (after the completion of 16 training sessions)]

Eligibility criteria

Inclusion criteria

  • More than 18 years of age
  • Clinical diagnosis of Multiple Sclerosis (MS)
  • Stable disease course without worsening more than 1 EDSS point over the last 3 months, -EDSS between 1.5 and 6 points
  • Must be able to maintain upright posture without any assistance for 30 seconds
  • Must be able to release a written informed consent.

Exclusion criteria

  • MS relapse within the previous three months;
  • Unable to comprehend the aims of the study and to follow test instructions;
  • Diagnosis of major depression (DSM-5);
  • Severe joint and/or bone disorders interfering with balance and gait (based upon clinical judgment);
  • Cardiovascular diseases;
  • Unconfirmed or uncertain diagnosis of MS (McDonald criteria)
  • Other concomitant neurological disease;
  • Patients already performing aerobic or walking exercise.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Italy · 1 center
  • Fondazione IRCCS Don Carlo Gnocchi — Milan

Identifiers

NCT: NCT06219304 · FISM_FAST

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗