Running, not recruitingPhase 1Relapsing MSNCT05755061

What it found

Still running

No result yet.

What was tested

Treatment tested

  • GEMS Plus

Compared with

  • GEMS

What it measured

Main measures

  • Change in cognitive processing speed

    Baseline; 6-months; 12-months

    Thinking and memory
  • Change in resting-state functional connectivity

    Baseline; 6-months; 12-months

    Nerve conduction tests

Other measures (1)

  • Change in thalamic volume

    Baseline; 6-months; 12-months

    MRI lesionsBrain volume loss

Who could take part

Relapsing MS · 16 to 65

Inclusion Criteria: * Definite MS diagnosis * Relapse-free for at least 30 days * Have Internet access on a device larger than a smartphone * Willingness and ability to travel to Kessler Foundation 3 times over a 12-month period * Be insufficiently physically active * Demonstrate low fall risk based on Activities Specific Balance Confidence scores * Demonstrate low contraindications for exercise * Right handedness * English as a primary language * Demonstrate low cognitive processing speed based on a Zoom-administered Symbol Digit Modalities Test Exclusion Criteria: * Acutely taken corticosteroids within 30 days of enrollment * Use an assistive device (i.e., cane, crutch, walker, rollator) for ambulation * Experienced a fall in the past 6 months * Have uncontrolled major depressive disorder or history of bipolar disorder or schizophrenia * Regularly taking medications that can affect cognition (e.g., antipsychotics, benzodiazepines) * Demonstrate contraindications for 3T MRI (i.e., having metal/shrapnel in the body, non-MRI compatible aneurysm clips) * Have severe cognitive impairment causing an inability to follow directions

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

About this trial

In the sponsor's words

This study is a randomized controlled trial (RCT) that compares the effects of two different 12-month aerobic walking exercise programs on cognitive processing speed (CPS), brain MRI, and other functional outcomes in 32 adults with multiple sclerosis (MS) who are able to walk without an assistive device but demonstrate slowed CPS. Participants (N=32) will initially undergo screening via telephone, and after satisfying relevant inclusion/exclusion criteria, will provide informed consent, followed by a baseline assessment of CPS remotely via a HIPAA-compliant virtual platform (i.e., Zoom for Healthcare). This assessment will also serve as a screen for ensuring impaired CPS. Following this virtual session, participants will come into Kessler Foundation (KF) and complete a 3-hour baseline assessment (T0) that includes a relatively short battery of neuropsychological tests, a 40-minute MRI scan, tests of walking function, a short questionnaire packet, followed by cardiopulmonary exercise testing on a motor-driven treadmill. Following T0, participants will be randomly assigned into one of the two aerobic walking ET programs that are remotely-delivered and supported by KF research assistants. As the conditions are delivered and supported remotely by KF personnel, the exercise itself takes place in the home/community setting. Both conditions involve behavior coaching via Zoom for Healthcare. The experimental condition involves high-frequency, high-intensity aerobic walking ET that exceeds the published guidelines for physical activity for adults with MS (GEMS+). GEMS + initially involves 10 minutes of moderate intensity aerobic walking exercise for 3 days per week and progresses to upwards of 40 minutes of vigorous intensity aerobic walking exercise for 5 days per week by month 12. The comparison condition involves mild-to-moderate aerobic walking exercise training that approximates published guidelines (GEMS). GEMS initially involves 10 minutes of light intensity aerobic walking exercise for 2 days per week and progresses up to 30 minutes of moderate intensity aerobic walking exercise for 3 days per week. Both conditions further will be monitored based on Fitbit-measured steps per exercise session. Of note, the sample size will be enrolled using 2 overlapping waves (Wave 1 = 14 participants, Wave 2 = 18 participants), 3 months apart. Participants will return to KF at the mid-point (i.e., T6) and end-point (i.e., T12) of the 12-month intervention period to complete the same assessments as T0. The T6 and T12 outcomes will be administered by treatment-blinded research assistants.

Loading reviews and guidelines…

History

    1. Started

      Feb 2023

    2. Main results due

      Feb 2025

    3. Finished

      Jan 2027

    Assembled by software from public sources and not checked by people. Each record links to its source. Report an error