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NCT Number: NCT06735651

Wild Blueberries for Gut, Brain, and Cardiometabolic Health in Prediabetes

The goal of this clinical trial is to determine the effectiveness of using a freeze-dried wild blueberry powder on cardiometabolic health, cognitive function, and gut microbiota composition in adult women with prediabetes.

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Key information

Age range

20 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Georgia State University

Atlanta, Georgia, 30303, United States

Location status: Recruiting

Location contact

Andrew Gerwitz, PhD

SUB_INVESTIGATOR

Brett J Wong, PhD

SUB_INVESTIGATOR

Elizabeth L Tighe, PhD

SUB_INVESTIGATOR

Rafaela G Feresin, PhD

CONTACT

[email protected]

404-413-1233

Rafaela G Feresin, PhD

PRINCIPAL_INVESTIGATOR

Tricia Z King, PhD

SUB_INVESTIGATOR

About this study

In the U.S., 35.3 million adults have type 2 diabetes mellitus (T2DM) and 96 million have prediabetes. Eight out of 10 people with T2DM die from cardiovascular disease. People with T2DM also have a 50% higher risk of developing dementia compared to healthy counterparts. Further, studies show that gut microbes play a major role in the development of T2DM. Prevention and treatment of T2DM focus on lifestyle changes including dietary modifications such as increased consumption of deep-colored fruits like berries. Blueberries are rich in fiber and phytochemicals and have several health benefits. We and others have shown that blueberry intake improves heart health in healthy men, hypertensive postmenopausal women, and men and women with metabolic syndrome. Yet, a comprehensive study in women with prediabetes that measures changes in cognitive performance and the underlying heart and gut health has not been conducted to date. Thus, the overall objective of this study is to investigate and bring forth evidence that wild blueberries improve gut, cardiometabolic, and cognitive function in women with prediabetes.

Therefore, this pilot six-week randomized, placebo-controlled parallel-arm clinical trial aims to investigate whether daily consumption of 22 g of freeze-dried wild blueberry powder improves gut, cardiometabolic, and cognitive function in women with prediabetes. Investigators hypothesize that daily consumption of wild blueberries will improve cardiometabolic parameters, gut dysbiosis, and cognitive impairments in our study population. To test these hypotheses, the following specific aims are proposed. To investigate whether daily consumption of 22 g of freeze-dried wild blueberry powder:

  • Reduces levels of fasting blood glucose (FBG), insulin, and HOMA-IR (homeostatic model assessment of insulin resistance) and improves lipid profile in women with prediabetes.
  • Reduces blood pressure and improves endothelial function in women with prediabetes.
  • Improves cognitive function (verbal memory and executive functions [inhibition, working memory, cognitive flexibility]) in women with prediabetes.
  • Favorably modulates gut microbiota composition in women with prediabetes.
  • Improves serum markers of oxidative stress and inflammation in women with prediabetes.

Additionally, whether changes in the gut microbiota are associated with changes in cardiometabolic and cognitive function outcomes and whether changes in cardiometabolic outcomes are associated with changes in cognitive function parameters will be explored.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women aged 20-65 years old
  • Prediabetes (fasting blood glucose 100-125 mg/dL and/or HbA1c percentage between 5.7-6.4)
  • Body Mass Index between 25-30 kg/m^2

Exclusion criteria

  • Allergies to berries
  • Use of insulin, antidiabetic, antibiotics, and anti-inflammatory drugs
  • Active cancer, gastrointestinal, renal, thyroid, stage 1 & 2 hypertension and other cardiovascular diseases, neurological diseases, or severe head injury
  • Smoking
  • Consumes greater than 2 alcoholic beverages per day
  • Consumes antioxidant, probiotic, and prebiotic supplements
  • Pregnant or Lactating
  • Actively participating in a weight loss program
  • Currently taking berry supplements or recently participated in another study taking berry supplements

Treatment and study plan

Wild Blueberry

Dietary Supplement

Daily consumption of 22 g of freeze-dried wild blueberry freeze-dried powder for 6 weeks

Placebo

Dietary Supplement

Daily consumption of 22 g of freeze-dried macronutrient-matched placebo powder for 6 weeks

Primary outcomes

  1. Blood Glucose

    Time frame: Baseline and 6 weeks

    Measurement of fasting blood glucose

  2. Ambulatory Blood Pressure

    Time frame: Baseline and 6 weeks

    Assessment of whole-day ambulatory blood pressure during daytime and nighttime periods.

Secondary outcomes

  1. Fasting Insulin

    Time frame: Baseline and 6 weeks

  2. Homeostasis model assessment-insulin resistance (HOMA-R)

    Time frame: Baseline and 6 weeks

    Calculated as fasting insulin (mU/mL) x fasting glucose (mg/dL)/405

  3. Blood Lipid Profile

    Time frame: Baseline and 6 weeks

    Measurement of blood lipid profile

  4. Gut Microbiota Composition

    Time frame: Baseline and 6 weeks

    Analysis of stool sample for determination of absolute levels of bacteria and relative species composition

  5. Global Cognitive Ability

    Time frame: Screening

    Measured using NIH Toolbox Picture Vocabulary test and Oral Reading Recognition

  6. Performance Validity

    Time frame: Baseline and 6 weeks

    Assessed using Rey 15

  7. Verbal Memory & Recognition

    Time frame: Baseline and 6 weeks

    Measured using Rey Auditory Verbal Learning Test with appropriate alternate forms

  8. Cognitive Inhibition

    Time frame: Baseline and 6 weeks

    Measured using Delis-Kaplan Executive Function System Color Word Interference, and NIH Toolbox Flanker Inhibitory Control and Attention

  9. Cognitive Flexibility

    Time frame: Baseline and 6 weeks

    Assessed using Delis-Kaplan Executive Function System Trails and Verbal Fluency Switching

  10. Working Memory

    Time frame: Baseline and 6 weeks

    Measured using Digit Span and NIH Toolbox List Sorting

  11. Processing Speed

    Time frame: Baseline and 6 weeks

    Measured using NIH Toolbox Pattern Comparison and Oral Symbol Digit tests

  12. Associative Memory

    Time frame: Baseline and 6 months

    Measured using NIH Toolbox Face Name Associative Memory Exam and Face Name Associative Memory Exam Delay tests

  13. Attention

    Time frame: Baseline and 6 weeks

    Assessed using Wechsler Adult Intelligence Scale - IV and Rey Auditory Verbal Learning Test Trial 1.

  14. Problem-Solving

    Time frame: Baseline and 6 weeks

    Assessed using NIH Toolbox Visual Reasoning Test

Other outcomes

  1. Reactive Hyperemia Index

    Time frame: Baseline and 6 weeks

    Assessment of endothelial function in response to increased shear stress using EndoPAT2000

  2. Pulse Wave Velocity

    Time frame: Baseline and 6 weeks

    Arterial Stiffness will be assessed by pulse wave velocity using SphygmCor

  3. Percent Maximal Microvascular Blood Flow

    Time frame: Baseline and 6 weeks

    Micro-vessel blood flow in response to local heating stimulus will be assessed using a Laser Doppler

  4. Circulating Markers of Inflammation and Oxidative Stress

    Time frame: Baseline and 6 weeks

    Measurement of concentrations of circulating markers of inflammation such as CRP and oxidative stress such as TBARS in blood plasma and serum samples.

  5. Urinary Polyphenolic Metabolites

    Time frame: Baseline and 6 weeks

    24-hour urine collection samples will be assessed for polyphenol metabolites

  6. Body Fat

    Time frame: Baseline and 6 weeks

    DEXA will be used to assess body fat.

Study contacts

Contact information is provided by the study sponsor or research team.

Rafaela G Feresin, PhD

CONTACT

[email protected]

404-413-1233

Sponsors and collaborators

Lead sponsor

Georgia State University

Other

Collaborators

  • Wild Blueberry Association of North America

Registry information

Official study title

Wild Blueberries for Gut, Brain, and Cardiometabolic Health in Female Adults With Prediabetes.

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Dec 16, 2024
Registry last updated
Mar 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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