COld Exposure With Controlled BReathing And Meditation in Patients With Multiple Sclerosis (COBRAMS)

Status unknownNot a drug-phase studyRelapsing MSNCT06280573

What it found

No results found

We found no results in the registry or in papers.

What was tested

Treatment tested

  • Wim Hoff method

What it measured

Main measures

  • concentration of pro-inflammatory cytokines

    12 weeks

    Immune response
  • concentration of markers of oxidative stress

    12 weeks

  • concentration of NfL

    12 weeks

    Blood or spinal fluid markers
  • concentration of GFAP

    12 weeks

    Blood or spinal fluid markers
  • concentration of ecDNA

    12 weeks

Other measures (7)

  • Expanded Disability Status Scale

    12 weeks

    Disability progression
  • Timed 25-Foot Walk

    12 weeks

    Disability progressionWalking and mobility
  • Nine-Hole Peg Test

    12 weeks

    Arm and hand function
  • Symbol Digit Modalities Test

    12 weeks

    Thinking and memory
  • Fatigue Scale for Motor and Cognitive Functions

    12 weeks

    Thinking and memoryFatigue
  • General Anxiety Disorder-7

    12 weeks

    Mood and sleep
  • Patient Health Questionnaire-9

    12 weeks

    Mood and sleep

Who could take part

Relapsing MS · 18 to 55 · EDSS 1.0 to 5.5

Show the full criteria

Inclusion criteria

* RRMS diagnosed according to the official 2020 McDonald's criteria, * age 18-55 years, * MS duration up to 10 years, * EDSS 1.0-5.5, * willingness to participate

Exclusion criteria

* relapse or corticosteroid treatment within 3 months prior to study enrollment * severe/unstable comorbidity

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

About this trial

In the sponsor's words

The goal of this interventional study is to test the effect of the anti-inflammatory and neuroprotective effects of this supplementary training program that includes breathing exercises, cold exposure, and meditation in patients diagnosed with multiple sclerosis. Researchers will compare the effect to control groups of MS patients without intervention.

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History

    1. Started

      Sept 2022

    2. Main results due

      Dec 2025

    3. Finished

      Dec 2025

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