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Active, Not Recruiting

NCT Number: NCT05755061

WEBCAMS: Walking Exercise for Brain and Cognition in Adults With Multiple Sclerosis

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

16 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Kessler Foundation

West Orange, New Jersey, 07052, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

GEMS Plus

Behavioral

12-months of home-based walking exercise that occurs 3-5 days per week. The program will progress up to intensities that exceed the published physical activity guidelines for adults with MS

GEMS

Behavioral

12-months of home-based walking exercise that occurs 3-5 days per week. The program will progress up to intensities that meet the published physical activity guidelines for adults with MS

Primary outcomes

  1. Change in cognitive processing speed

    Time frame: Baseline; 6-months; 12-months

    Participants will undertake the Symbol Digit Modalities Test as a cognitive test of cognitive processing speed as one of the primary study outcomes

  2. Change in resting-state functional connectivity

    Time frame: Baseline; 6-months; 12-months

    Participants will undertake an fMRI scan to measure resting-state functional connectivity between the thalamus and other brain regions as one of the primary study outcomes

Secondary outcomes

  1. Change in thalamic volume

    Time frame: Baseline; 6-months; 12-months

    Participants will undertake an MRI scan to measure volume of the thalamus as a secondary study outcome

Other outcomes

  1. Change in aerobic fitness

    Time frame: Baseline; 6-months; 12-months

    Participants will undertake a maximal, graded exercise test on a treadmill to measure aerobic fitness

Sponsors and collaborators

Lead sponsor

Kessler Foundation

Other

Registry information

Official study title

Long-Term Aerobic Walking Exercise for Restoring Cognition and Brain in People With Multiple Sclerosis

Important dates

Study start
2023
Primary completion
2025
Study completion
2026
First posted
Mar 6, 2023
Registry last updated
Aug 28, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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