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NCT07475377Recruiting

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

Source: ClinicalTrials.gov · Last updated 25 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
22 (estimated)
First submitted
11 Mar 2026
Start date
Aug 2026
Primary completion date
Sept 2027
Lead sponsor
University of Alabama at Birmingham
NCT number
NCT07475377

What you commit to

  • Study type: Interventional
  • Planned participants: 22
  • From Aug 2026 to the primary completion date, Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Relapse within previous 30 days
  • Current use of GLP-1 or use within previous 3 months

Other

  • Actively engaged in a weight loss program or unwilling to follow assigned eating schedule
  • 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)

Who the study is looking for

  • 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

Age in the registry: 18 years to 64 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alabama at Birmingham
Coordinator of this site? Confirm its status
BirminghamUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.