Skip to content

Effect of Blueberries on Cognition and Body Composition in Elderly With Mild Cognitive Decline

The Effect of Blueberry Consumption on Cognition and Body Composition in Elderly Who Are Experiencing Mild Cognitive Decline

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01515098
Acronym
BERRY
Enrollment
123
Registered
2012-01-23
Start date
2012-01-31
Completion date
2015-03-31
Last updated
2022-03-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Cognitive Decline

Brief summary

Purpose: The purpose of this study is to examine the effect of blueberry consumption on cognitive decline and body composition in humans. Hypothesis 1: Adults with mild cognitive decline who consume blueberries will experience an improvement in cognitive abilities as measured by a standardized battery of tests, relative to those who consume a placebo. Hypothesis 2: Adults with mild cognitive decline who consume blueberries will evidence an increase in processing speed and an improvement in memory abilities as measured in an electrophysiological paradigm and compared to those who consume a placebo. Hypothesis 3: Daily intake of 35 g freeze-dried blueberries will improve body composition (fat mass vs. lean mass). Hypothesis 4: Daily intake of 35 g freeze-dried blueberries will decrease oxidative stress and inflammatory markers.

Interventions

DIETARY_SUPPLEMENTFreeze-dried blueberries

Wild blueberries, freeze-dried and pulverized

DIETARY_SUPPLEMENTDextrose Placebo

Placebo developed to closely match blueberry powder.

Sponsors

University of North Carolina, Chapel Hill
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to 79 Years
Healthy volunteers
Yes

Inclusion criteria

* Men and women age 65 and older * BMI between 18.5 and 34.5 * Close individual to report memory decline

Exclusion criteria

* History of central nervous system or psychiatric disorders * Dementia or Alzheimer's diagnosis * Diabetes * Smoking \>20 cigarettes/day * Gastrointestinal/digestive disorders * Uncontrolled chronic disease

Design outcomes

Primary

MeasureTime frameDescription
Change in cognitive test performanceBaseline, 180 daysMeasured by CANTAB
Change in brain activity (N200, P300) related to cognitive abilities as measured by event-related potentials (ERP)Baseline, 180 daysRecognition memory, speed of processing, and memory consolidation as measured by the electrophysiological technique known as event-related potentials (ERP)

Secondary

MeasureTime frameDescription
Change in body mass distributionBaseline, 180 daysDXA scans to measure body composition at baseline and outcome will be compared for differences
Change in oxidative stress and inflammatory markers as measured in blood and urineBaseline, 180 daysOxidative stress and inflammatory markers will be measured in blood and compared between baseline and outcome.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026