Actively Recruiting

Phase Not Applicable
Age: 18Years - 64Years
All Genders
NCT06450977

Remote Evaluation of MIND Diet

Led by University of Illinois at Urbana-Champaign · Updated on 2024-06-27

40

Participants Needed

1

Research Sites

133 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Remote Evaluation of MIND Diet

Who Can Participate

Age: 18Years - 64Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  1. Individuals aged 18-64 years old
  2. Self-reported diagnosis of Multiple sclerosis (MS)
  3. 20/20 or corrected vision
  4. No other neurodegenerative disease diagnosis
  5. Stable disease-modifying therapy (DMT) within 6 months
  6. Not Pregnant or lactating
  7. No food allergies or intolerances
  8. Able to consume study meals
  9. Not enrolled in another dietary, exercise, or medication study during the study
  10. Access to a computer/laptop with internet
Not Eligible

You will not qualify if you...

  1. Individuals younger than 18 or older than 64 years old
  2. No self-reported diagnosis of Multiple sclerosis (MS)
  3. Not 20/20 or uncorrected vision
  4. Other neurodegenerative disease diagnosis
  5. Disease modifying therapy (DMT) less than 6 months
  6. Pregnant or lactating
  7. Food allergies or intolerances
  8. Not able to consume study meals
  9. Enrolled in another dietary, exercise, or medication study during the study
  10. No access to a computer/laptop with internet

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Illinois Urbana-Champaign

Urbana, Illinois, United States, 61801

Actively Recruiting

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Research Team

N

Naiman Khan, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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