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RecruitingNCT06137339AvoCogUpdated Aug 22, 2024

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

An interventional study of Avocado Group in Brain Aging, sponsored by University of Kansas Medical Center. Recruiting at 1 site in United States. Open to participants aged 65 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-22.

Sponsored by University of Kansas Medical Center · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as recruiting.
  • Started Apr 2024; still recruiting 2 years 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
65 Years to 85 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Brain Aging

Keywords

  • Older Adults
  • Brain Health
  • Avocado
  • Brain Imaging
  • Cognition
  • Dietary Intervention
03

In context

Lead sponsor

University of Kansas Medical Center is the lead sponsor of 483 studies on the registry; 113 are open to participants now.

Of its 38 completed or terminated interventional studies of FDA-regulated products, 24 (63%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Males and females aged 65-85 years
  • Good general health with no concomitant disease
  • BMI 18.5 - 35 kg/m2
  • Mini Mental State Exam ≥26
  • Reports consuming ≤2 medium avocados per month
  • Reports consuming ≤3 servings of carotenoid-rich foods per week and ≤3 servings of fruits and vegetables per day
  • Skin carotenoid content \<400

Exclusion criteria

Exclusion Criteria:

  • Unwilling or unable to consume avocado
  • Latex allergy
  • Consistently taking lutein + zeaxanthin supplements
  • Skin carotenoid content ≥400
  • Central neurological disease such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, stroke, brain tumor, etc.
  • Serious medical risk: cancer requiring chemotherapy or radiation within the past 5 years, recent cardiac event (i.e. heart attack, etc.)
  • Diabetes mellitus or uncontrolled hypertension
  • Use of psychoactive or investigational medications
  • Consumption of ≥3 alcoholic drinks per day or substance abuse
  • Unable to undergo MRI
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
70 participants (estimated)

Study arms

  • Experimental
    Avocado Group

    Participants will consume 1 avocado per day and receive education to maintain usual caloric intake for 12 weeks and participate in 4 study visits.

    Other: Avocado Group

  • No intervention
    No Diet Modification Group

    Participants will continue their normal dietary pattern for 12 weeks and participate in 4 study visits.

Interventions

  • OtherAvocado Group

    Participants will consume provided avocados daily and track consumption for the duration of the study. Participants will be adding avocados to their diet and will receive education on maintaining usual diet.

06

What researchers measure

Primary outcomes

  1. Change in brain activity

    MRI will be used to measure changes in brain activity during resting state, a working memory task, and executive function task.

    Time frame: Baseline and 12 weeks

Secondary outcomes

  1. Changes in cerebral blood flow

    MRI will be used to measure change in cerebral blood flow.

    Time frame: Baseline and 12 weeks

  2. Changes in memory and executive function

    NIH Toolbox will be used to measure change in cognition throughout the study.

    Time frame: Baseline and 12 weeks

07

Study locations

1 of 1 sites recruiting
  • University of Kansas Medical Center
    Kansas City, Kansas 66160, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 22, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06137339
Lead sponsor
University of Kansas Medical Center
Collaborators
Avocado Nutrition Center
Responsible party
Matthew Taylor (Dr. Matthew K Taylor, PhD, RD, University of Kansas Medical Center) — Principal investigator
First posted
Nov 18, 2023
Start date
Apr 9, 2024
Primary completion
Dec 2025 (estimated)
Completion
Dec 2025 (estimated)
Last update
Aug 22, 2024

Study contacts

Emma Kelly, MS
Contact
ekelly9@kumc.edu
913-588-7683
Matthew Taylor, PhD
Contact
mtaylor3@kumc.edu
913-588-5363

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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