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NCT Number: NCT07475377

Understanding the Impact of Meal Timing on Neurological Health in Adults With Multiple Sclerosis

The goal of this clinical trial is to learn if the time an individual eats each day impacts neurological health in people with multiple sclerosis. The main questions the investigators are asking are:

1. Does meal timing affect biomarkers of neuronal health (neurofilament light chain [NfL] and BDNF) and inflammation (IL-6, IL-17, TNF-ɑ) in adults with MS. 2. Does meal timing affect expression of circadian clock genes and genes associated with autophagy in adults with MS.

Participants will be instructed to start and stop eating at specific times each day based on their group assignment and their personal schedule. They will respond to prompts sent to them on their smartphone to record the times they start and stop eating each day.

As a secondary goal, the study will also explore the feasibility of including translocator protein (TSPO)-PET imaging of neuroinflammation in future clinical trials of TRE in people with MS. To accomplish this, imaging will be completed in a subset of 8 participants at the beginning and end of the study.

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Key information

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Alabama at Birmingham

Birmingham, Alabama, 35294, United States

Location contact

Brooks C Wingo

PRINCIPAL_INVESTIGATOR

Kathryn Green

CONTACT

[email protected]

About this study

The mechanisms underlying the relationship between diet and MS are not well understood. A leading theory is that diet affects disease progression and symptoms through modulation of neuroinflammation. Previous studies in participants with other conditions suggest that time restricted eating (TRE) may reduce inflammation by improving circadian rhythms. If this holds true in people with MS, it may explain how TRE improves clinical outcomes of cognitive and physical function as seen in a previous trial. It may also explain diurnal fluctuations in pain and fatigue experienced by people within MS.

Although a previous study measured the effect of TRE on physical and cognitive function, as well as pain and fatigue, it was a single arm study and did not measure the hypothesized mechanisms of action. Therefore, the purpose of this pilot study is to examine the effects of TRE on neurological, inflammatory, and circadian markers in adults with MS.

Adults with relapsing forms of MS (relapsing remitting [RRMS] or secondary progressive [SPMS], n = 22) will be randomly assigned to either a TRE group that will eat all food within an 8-hour window each day (treatment group) or a group that will eat over 12 or more hours each day for 12 weeks.

Further, investigators will assess the feasibility of using Positron Emission Tomography (PET) imaging to measure changes in neuroinflammation with TRE. This exploratory aim will be completed in a subset of participants (n=8), and will be used to finalize imaging protocols and determine feasibility of including translocator protein (TSPO)-PET imaging of neuroinflammation in future clinical trials of TRE in people with MS.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosed with relapsing remitting or secondary progressive multiple sclerosis (RRMS or SPMS)
  • If on disease modifying therapy (DMTs), stable for 6 months
  • If not on DMTs, no DMT usage within previous 6 months
  • BMI 18.5-50 kg/m2
  • Access to a smartphone
  • Responsible for personal eating schedule or able to have input into schedule

Exclusion criteria

  • Relapse within previous 30 days
  • Actively engaged in a weight loss program or unwilling to follow assigned eating schedule
  • Current use of GLP-1 or use within previous 3 months
  • Regularly fasts > 12 hours/day
  • Employed in night shift or rotating shift work
  • Unable to walk 25 feet with or without assistive device (EDSS > 6.5).
  • Current use of insulin or sulfonylurea agents
  • Pregnant or breastfeeding
  • Currently enrolled in another trial that would confound results (e.g., exercise studies or other diet studies)

Treatment and study plan

Time restricted eating

Behavioral

Participants will eat all meals within 8 hours/day and fast for the remaining 16 hours/day.

Unrestricted eating

Behavioral

Participants will eat all meals over 12 or more hours/day.

Primary outcomes

  1. Neurofilament light chain

    Time frame: Baseline and 12 weeks

Secondary outcomes

  1. Brain Derived Neurotrophic Factor

    Time frame: Baseline and 12 weeks

  2. Interleukin-6

    Time frame: Baseline and 12 weeks

  3. Interleukin-17

    Time frame: Baseline and 12 weeks

  4. Tumor necrosis factor-alpha

    Time frame: Baseline and 12 weeks

  5. Change in circadian gene expression

    Time frame: Baseline, 12 weeks

    Change in expression of the following genes: CLOCK, PER2, BMAL1, PER1, PER2, CRY1, CRY2, REV-ERBA/NR1D1

  6. Change in expression of autophagy genes

    Time frame: Baseline, 12 weeks

    Change in expression of the following autophagy-related genes: LC3A, ATG5, ATG7, ATG12, LAMP2

  7. Multiple Sclerosis Functional Composite

    Time frame: Baseline and 12 weeks

Other outcomes

  1. Neuroinflammation

    Time frame: Baseline, 12 weeks

    Neuroinflammation will be measured with translocator protein (TSPO)-PET imaging

Study contacts

Contact information is provided by the study sponsor or research team.

Brooks C Wingo, PhD

CONTACT

[email protected]

205-934-5982

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Collaborators

  • Paralyzed Veterans of America Research Foundation

Registry information

Acronym: Meal Time MS

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 16, 2026
Registry last updated
Jul 13, 2026

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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