Actively Recruiting

Phase Not Applicable
Age: 65Years - 75Years
All Genders
Healthy Volunteers
NCT06192407

Fatty Acid Modulation of Brain Function in Older Adults

Led by University of Vermont · Updated on 2025-09-17

60

Participants Needed

1

Research Sites

237 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this crossover study, the investigtors will administer two experimental diets in a random order for one week, and each experimental diet will be preceded by a one-week, low fat control diet for a total four-week study period. The goal is to study how the fatty acid content of the diet affects brain functioning in healthy adults aged 65-75 years. One experimental diet will have a high palmitic acid (PA)/oleic acid (OA) ratio (HPA), typical of the North American diet. The other experimental diet will have a low PA/OA ratio (HOA), typical of the Mediterranean Diet. All allowed food and drink (except water) will be provided by the investigative team, and compliance will be enhanced by constant, intense dietary surveillance by a registered dietitian.

CONDITIONS

Official Title

Fatty Acid Modulation of Brain Function in Older Adults

Who Can Participate

Age: 65Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and women aged 65 to 75 years
  • Normal cognition as assessed by study cognitive tests
  • Healthy with body mass index (BMI) between 20 and 40 kg/m2
Not Eligible

You will not qualify if you...

  • Significant cognitive or behavioral impairment or use of medications for these conditions
  • Hormone replacement therapy within the past 3 months
  • Hyper-androgenic conditions
  • HbA1C 7.5% or higher or fasting plasma glucose 130 mg/dL or higher
  • Type 2 diabetes treated with medications other than metformin
  • Use of nicotine or intake of caffeine or alcohol during the study
  • Habitual fat intake less than 25% of calories or strict vegetarian diet
  • Sleep apnea requiring continuous positive airway pressure at night
  • Lung, heart failure or treatment, liver, kidney disease, cancer, or other medical disorders causing inflammation or cognitive problems
  • Actively training for athletic events or competitive sports
  • Allergy or intolerance to any study-provided foods

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 Vermont

Burlington, Vermont, United States, 05401

Actively Recruiting

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Research Team

J

Julie Dumas, Ph.D.

CONTACT

J

Jenna Makarewicz, B.S.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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