No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 64
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
22 (estimated)
Sponsor
University of Alabama at Birmingham · Other
Who this trial is looking for
This trial is looking for adults with multiple sclerosis to learn if when they eat affects their neurological health. Participants will need to eat at specific times each day and report their eating schedule via smartphone prompts.
Are You a Good Fit for This Trial?
Must not be takingGLP-1
You may be able to join if
I have been diagnosed with relapsing remitting or secondary progressive multiple sclerosis.
I have been stable on any disease modifying therapy for 6 months.
I have not used disease modifying therapies in the past 6 months.
I have a BMI between 18.5 and 50.
I have access to a smartphone.
I can manage my own eating schedule.
You may not be able to join if
I have had a relapse in the past 30 days.
I am actively engaged in a weight loss program.
I currently use GLP-1 medications or have used them in the past 3 months.
I regularly fast for more than 12 hours a day.
I work night shifts or rotating shifts.
I cannot walk 25 feet with or without an assistive device.
I currently use insulin or sulfonylureas.
I am pregnant or breastfeeding.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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…
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.
Trial Locations
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Eligibility Criteria
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 pe…
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)
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