Gut health meets diet: a new angle on managing multiple sclerosis
NCT ID NCT07789171
First seen Aug 27, 2026 · Last updated Aug 28, 2026 · Updated 1 time
Summary
This trial tests whether adding a synbiotic supplement to a Mediterranean diet can improve quality of life and reduce disability in people with relapsing-remitting multiple sclerosis. Participants follow the diet for 12 weeks and take either a synbiotic or a placebo pill daily. Researchers measure changes in quality of life, disability scores, body measurements, and mood.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A synbiotic supplement (probiotic plus prebiotic) taken alongside a Mediterranean diet plan
- What this could lead to
- If it works, this could point toward a dietary approach that helps manage MS symptoms and improve daily life.
- What could go wrong
- The trial is small and early, so results may not apply broadly. Supplements can cause digestive discomfort, and the diet may be hard to follow.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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38 people
The number who actually took part.
- Started
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Mar 2020
- Finished
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Nov 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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19 to 64 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Being aged 19-64 years * Having an EDSS score of 6.5 or below, * Being clinically diagnosed with RRMS and being under the care of the relevant outpatient clinic, * Having had no attacks in the last month, * Not receiving immunosuppressive drug therapy (Cyclophosphamide, Methotrexate, Azathioprine, Mitoxantrone, Mycophenolate Mofetil) * Not being deficient in vitamin D * Being a female diagnosed at least one year ago (to ensure a homogeneous gender distribution in the group and because the incidence of MS is higher in females) Exclusion Criteria: * Individuals who have used probiotics/synbiotics or antibiotics within the last two weeks prior to participating in the study, either on a doctor's advice or of their own accord, and who will be required to use probiotics/synbiotics or antibiotics during the study period. * Individuals with enteric inflammation, advanced liver or kidney disease, * Individuals diagnosed by a physician with diabetes, hyperlipidemia, gout, chronic renal failure, or liver disease requiring special medical nutrition therapy, * Pregnant or lactating women, * Individuals with a body mass index of 30 kg/m2 or above, * Individuals who have participated in another clinical trial within the last month, * Individuals who have previously reported sensitivity to probiotic/synbiotic treatment, * Individuals whose standard medical treatment or medication dosage is changed or planned to change during the study period, * Individuals who cannot ensure continuity in research follow-up
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hacettepe University
Ankara, Ankara, 06230, Turkey (Türkiye)
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