Optimized Tailored Interventions in Metabolic and Lifestyle Outcomes (OPTIMAL)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-64
SponsorUniversity of Illinois at Urbana-Champaign

About 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 brain and heart health relative to a healthy control diet in middle-aged adults. Our research team will evaluate three different groups: the first group will be chosen using a predictive analytics model that predicts who will benefit most from the MIND diet, the second group will follow the MIND diet without being pre-selected, and the third group will eat a standard healthy diet to serve as a comparison.

The main questions it aims to answer are:

Does the MIND diet improve cognitive performance and heart health relative to a control diet? How does the health impact of the MIND diet in participants pre-identified through predictive analytics compare to those without such pre-selection? Which of the three groups - predictive analytics selected MIND diet group, standard MIND diet group, or healthy control - demonstrate the most significant improvements in cognitive and cardiovascular health over the course of the trial?

Participants will:

Consume one meal that follows the MIND diet or a control meal every day for 3 months. Visit the lab before and after the 3 months of meals for tests. Keep a record of the food they eat during the study.

Eligibility criteria

Qualifiers

45-64 years of age

20/20 or corrected vision

No food allergies or intolerances

Not pregnant, lactating, or have given birth in the past 12 months

Disqualifiers

Non-consent of participant

Above 64 or below 45 years of age

Vision not 20/20 or corrected

Food allergies or intolerances

Trial design

Treatments tested in this trial

  • MIND Diet
  • Control Diet

Treatment groups

72 Participants
are divided into 3 treatment groups