MIND Diet for Multiple Sclerosis
(REMIND Trial)
Trial Summary
What is the purpose of this trial?
The goal of this clinical trial is to learn if increasing adherence to a Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) diet pattern improves thinking ability and memory compared to a healthy control diet in persons with Multiple Sclerosis (MS). The main question it aims to answer is: Does the MIND diet improve cognitive performance relative to a control diet in persons with MS? Participants will: Consume one meal that follows the MIND diet or a control meal every day for 3 months, complete online surveys and cognitive testing before and after, and keep a record of the food they eat during the study.
Will I have to stop taking my current medications?
The trial does not specify if you need to stop taking your current medications. However, it requires that your disease-modifying therapy (DMT) has been stable for at least 6 months.
What data supports the effectiveness of the MIND Diet treatment for Multiple Sclerosis?
Research suggests that the MIND diet, which combines elements of the Mediterranean and DASH diets, may have neuroprotective effects and is associated with reduced odds of developing multiple sclerosis. Additionally, the MIND diet has been linked to better cognitive performance and a decreased risk of dementia, indicating its potential benefits for brain health.12345
Is the MIND diet safe for humans?
The MIND diet, which combines elements of the Mediterranean and DASH diets, has been studied for its potential health benefits, including neuroprotective effects and improved cognitive performance. There is no specific mention of safety concerns in the available research, suggesting it is generally considered safe for human consumption.12346
How is the MIND Diet treatment unique for multiple sclerosis?
Research Team
Naiman Khan, PhD
Principal Investigator
University of Illinois Urbana-Champaign
Eligibility Criteria
This trial is for people aged 18-64 with Multiple Sclerosis, good or corrected vision, and stable MS treatment. They shouldn't have other neurodegenerative diseases, be pregnant or lactating, have food allergies/intolerances, or be in another diet/exercise/medication study.Inclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants consume one meal per day following the MIND diet or a control diet for 12 weeks, complete online surveys and cognitive testing, and keep a food record
Follow-up
Participants are monitored for cognitive performance improvements and adherence to the diet
Treatment Details
Interventions
- Control Diet
- MIND Diet
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Illinois at Urbana-Champaign
Lead Sponsor