Actively Recruiting

Phase Not Applicable
Age: 65Years - 85Years
All Genders
Healthy Volunteers
NCT06137339

AvoCog - the Effect of Daily Avocado Intake on Cognitive Function in Older Adults

Led by University of Kansas Medical Center · Updated on 2024-08-22

70

Participants Needed

1

Research Sites

85 weeks

Total Duration

On this page

Sponsors

U

University of Kansas Medical Center

Lead Sponsor

A

Avocado Nutrition Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to determine if adding avocados to the diet of impacts cognition in 70 older adults, age 65-85, without dementia. We will test for change in functional MRI, cognitive performance, and brain blood flow. Intervention group participants will be asked to consume 1 avocado per day for 12 weeks. Participants in the control group will be asked to continue their normal intake for 12 weeks. Throughout the study, participants will be asked to perform cognitive tests, MRI, blood tests, and questionnaires.

CONDITIONS

Official Title

AvoCog - the Effect of Daily Avocado Intake on Cognitive Function in Older Adults

Who Can Participate

Age: 65Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Males and females aged 65-85 years
  • Good general health with no concomitant disease
  • Body mass index between 18.5 and 35 kg/m2
  • Mini Mental State Exam score of 26 or higher
  • Consuming 2 or fewer medium avocados per month
  • Consuming 3 or more servings of carotenoid-rich foods per week and 3 or more servings of fruits and vegetables per day
  • Skin carotenoid content less than 400
Not Eligible

You will not qualify if you...

  • Unwilling or unable to consume avocado
  • Allergy to latex
  • Taking lutein plus zeaxanthin supplements regularly
  • Skin carotenoid content 400 or higher
  • Central neurological diseases such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, stroke, or brain tumor
  • Serious medical risks such as cancer treated by chemotherapy or radiation within the past 5 years, or recent heart attack
  • Diabetes mellitus or uncontrolled high blood pressure
  • Use of psychoactive or investigational medications
  • Drinking 3 or more alcoholic drinks per day or substance abuse
  • Unable to undergo MRI

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Kansas Medical Center

Kansas City, Kansas, United States, 66160

Actively Recruiting

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Research Team

E

Emma Kelly, MS

CONTACT

M

Matthew Taylor, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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