AvoCog - the Effect of Daily Avocado Intake on Cognitive Function in Older Adults
- Conditions
- Brain Aging
- Interventions
- Other: Avocado Group
- Registration Number
- NCT06137339
- Lead Sponsor
- University of Kansas Medical Center
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 70
- 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
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Avocado Group 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.
- Primary Outcome Measures
Name Time Method Change in brain activity Baseline and 12 weeks MRI will be used to measure changes in brain activity during resting state, a working memory task, and executive function task.
- Secondary Outcome Measures
Name Time Method Changes in cerebral blood flow Baseline and 12 weeks MRI will be used to measure change in cerebral blood flow.
Changes in memory and executive function Baseline and 12 weeks NIH Toolbox will be used to measure change in cognition throughout the study.
Trial Locations
- Locations (1)
University of Kansas Medical Center
🇺🇸Kansas City, Kansas, United States