Wild Blueberries for Gut, Brain, and Cardiometabolic Health in Prediabetes
Recruiting · NCT06735651 · Interventional (participants receive a specific treatment) · Lead sponsor: Georgia State University
View the official record on ClinicalTrials.gov →Interventions studied
PlaceboWild Blueberry
What this trial is about
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.
Who can take part
Age range
20 Years to 65 Years
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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
Where it is running
1 location listed across 1 US state.
- Georgia State University - Atlanta, Georgia, United States