RECRUITING

Remote Evaluation of MIND Diet

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Remote Evaluation of MIND Diet

Quick Facts

Study Start:2024-06-07
Study Completion:2026-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06450977

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 64 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Individuals aged 18-64 years old
  2. 2. Self-reported diagnosis of Multiple sclerosis (MS)
  3. 3. 20/20 or corrected vision
  4. 4. No other neurodegenerative disease diagnosis
  5. 5. Stable disease-modifying therapy (DMT) within 6 months
  6. 6. Not Pregnant or lactating
  7. 7. No food allergies or intolerances
  8. 8. Able to consume study meals
  9. 9. Not enrolled in another dietary, exercise, or medication study during the study
  10. 10. Access to a computer/laptop with internet
  1. 1. Individuals younger than 18 or older than 64 years old
  2. 2. No self-reported diagnosis of Multiple sclerosis (MS)
  3. 3. Not 20/20 or uncorrected vision
  4. 4. Other neurodegenerative disease diagnosis
  5. 5. Disease modifying therapy (DMT) less than 6 months
  6. 6. Pregnant or lactating
  7. 7. Food allergies or intolerances
  8. 8. Not able to consume study meals
  9. 9. Enrolled in another dietary, exercise, or medication study during the study
  10. 10. No access to a computer/laptop with internet

Contacts and Locations

Study Contact

Naiman Khan, PhD
CONTACT
2173001667
nakhan2@illinois.edu

Principal Investigator

Naiman Khan, PhD
PRINCIPAL_INVESTIGATOR
University of Illinois Urbana-Champaign

Study Locations (Sites)

University of Illinois Urbana-Champaign
Urbana, Illinois, 61801
United States

Collaborators and Investigators

Sponsor: University of Illinois at Urbana-Champaign

  • Naiman Khan, PhD, PRINCIPAL_INVESTIGATOR, University of Illinois Urbana-Champaign

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-07
Study Completion Date2026-12-31

Study Record Updates

Study Start Date2024-06-07
Study Completion Date2026-12-31

Terms related to this study

Keywords Provided by Researchers

  • Executive Function
  • MIND
  • Dietary Pattern
  • Telehealth

Additional Relevant MeSH Terms

  • Multiple Sclerosis
  • Cognitive Change
  • Nutrition, Healthy