Investigating the Effects of Acute Intermittent Hypoxia on Neuroplasticity in Persons With Multiple Sclerosis

RecruitingNot a drug-phase studyRelapsing and progressiveNCT06390930

What it found

Still running

No result yet.

What was tested

Treatment tested

  • Acute Intermittent Hypoxia

Placebo

  • Sham Acute Intermittent Hypoxia

What it measured

Main measures

  • Motor Evoked Potentials (MEPs) in First Dorsal Interosseous (FDI)

    Immediately before, immediately after, and 60 minutes after the intervention.

    Myelin repairNerve conduction tests
  • Changes in Spinal Reflex Threshold

    Immediately before the intervention and immediately after the intervention.

  • Threshold For Detecting Passive Joint Movement

    Immediately before the intervention and immediately after the intervention.

  • Accuracy of Direction Estimation of Passive Joint Movement

    Immediately before the intervention and immediately after the intervention.

Other measures (9)

  • Grip Strength

    Immediately before the intervention and immediately after the intervention.

    Arm and hand functionPhysical function
  • Pinch Strength

    Immediately before the intervention and immediately after the intervention.

    Physical function
  • Index Finger Abduction Force

    Immediately before the intervention and immediately after the intervention.

  • Nine-Hole Peg Test

    Immediately before the intervention and immediately after the intervention.

    Arm and hand function
  • Symbol Digit Modalities Test

    Immediately before the intervention and immediately after the intervention.

    Thinking and memory
  • Box and Block Test

    Immediately before the intervention and immediately after the intervention.

    Arm and hand function
  • Modified Ashworth Scale

    Immediately before the intervention and immediately after the intervention.

    Spasticity
  • Ipsilateral Joint Position Matching Task

    Immediately before the intervention and immediately after the intervention.

  • Visual Analog Pain Scale

    Immediately before the intervention and immediately after the intervention.

    Pain

Who could take part

Relapsing and progressive · 18 to 75

Show the full criteria

Inclusion criteria

* Diagnosis of relapsing-remitting MS according to the McDonald criteria, over 5 years ago * Relapse free for at least 6 months * Expanded Disability Status Scale (EDSS) ≤7 * Index finger abduction strength \<5 according to Medical Research Council Scale, or 9-Hole Peg Test score >20 seconds in at least one hand * Stable disease modifying therapies for at least 6 months * Individuals taking dalfampridine will be eligible if taking the same daily dose for at least 2 months prior to screening

Exclusion criteria

* Another diagnosis (e.g., peripheral neuropathies or orthopedic) affecting upper limb function * Mini-Mental State Examination (MMSE) score \<24 * Modified Ashworth Scale score >3 on elbow joint * Uncontrolled hypertension or hypotension (outside 140/90 and 85/55 mmHg) * History of epilepsy, chronic obstructive pulmonary disease, or sleep apnea * Unstable medical conditions, ongoing upper limb therapy, or musculoskeletal pain * Pregnancy as confirmed by urine test

As registered. Criteria can change, so ask the trial team or your neurologist.

Contact details on the registry

About this trial

In the sponsor's words

This study seeks to explore changes in the neural pathways and arm function following a breathing intervention in the multiple sclerosis (MS) population. The breathing intervention, known as Acute Intermittent Hypoxia (AIH), involves breathing brief bouts of low levels of oxygen. Research has found AIH to be a safe and effective intervention resulting in increased ankle strength in people with MS. Here, the study examines arm and hand function before and after AIH. In order to better understand the brain and spinal cord response to AIH, the investigators will measure muscle response, and signals sent from the brain to the arm muscles before and after AIH.

Papers

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    History

      1. Started

        Feb 2025

      2. Main results due

        Jul 2026

      3. Finished

        Jul 2027

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