Status:

RECRUITING

Effects of Wild Blueberry Consumption on Brain Function in Elderly

Lead Sponsor:

Maastricht University Medical Center

Collaborating Sponsors:

Wild Blueberry Association of North America

Conditions:

Brain Insulin-sensitivity

Brain Vascular Function

Eligibility:

All Genders

60-75 years

Phase:

NA

Brief Summary

Impaired brain vascular function precedes the development of reduced cognitive performance, while brain insulin-resistance is associated with cognitive decline. Evidence from epidemiological studies h...

Eligibility Criteria

Inclusion

  • Men and women, aged between 60-75 years
  • BMI between 25-35 kg/m2 (overweight or obese)
  • Fasting plasma glucose \< 7.0 mmol/L
  • Fasting serum total cholesterol \< 8.0 mmol/L
  • Fasting serum triacylglycerol \< 4.5 mmol/L
  • Systolic blood pressure \< 160 mmHg and diastolic blood pressure \< 100 mmHg
  • Stable body weight (weight gain or loss \< 3 kg in the past three months)
  • Willingness to give up being a blood donor from 8 weeks before the start of the study, during the study and for 4 weeks after completion of the study.
  • No difficult venipuncture as evidences during the screening visit.

Exclusion

  • Allergy or intolerance to berries
  • Left-handedness
  • Current smoker, or smoking cessation \< 12 months
  • Diabetic patients
  • Familial hypercholesterolemia
  • Abuse of drugs
  • More than 3 alcoholic consumptions per day
  • Use of products or dietary supplements known to interfere with the main outcomes as judged by the principal investigators
  • Use medication to treat blood pressure, lipid, or glucose metabolism
  • Use of an investigational product within another biomedical intervention trial within the previous 1-month
  • Severe medical conditions that might interfere with the study, such as epilepsy, asthma, kidney failure or renal insufficiency, chronic obstructive pulmonary disease, inflammatory bowel diseases, auto inflammatory diseases, and rheumatoid arthritis.
  • Active cardiovascular disease like congestive heart failure or cardiovascular event, such as an acute myocardial infarction or cerebrovascular accident.
  • Contra-indications for MRI imaging (e.g., pacemaker, surgical clips/material in body, metal splinter in eye, claustrophobia)

Key Trial Info

Start Date :

December 5 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

August 31 2026

Estimated Enrollment :

36 Patients enrolled

Trial Details

Trial ID

NCT07177781

Start Date

December 5 2024

End Date

August 31 2026

Last Update

September 17 2025

Active Locations (1)

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1

Maastricht University, Departement of Nutrition and Movement Sciences

Maastricht, Limburg, Netherlands, 6200 MD