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The Effect of Wild Blueberry Consumption on Glucose Regulation in Healthy Adults

The Effect of Wild Blueberry Consumption on Diabetes: Evaluation of Glucose Regulation, Gastrointestinal Hormones and Satiety in Healthy Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03192605
Enrollment
17
Registered
2017-06-20
Start date
2017-05-15
Completion date
2017-06-02
Last updated
2017-06-20

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

Conditions

Diabetes

Brief summary

The objective of the study is to determine how wild blueberry consumption affects glucose regulation, gastrointestinal hormones and satiety in healthy adults.

Detailed description

Healthy men and women (ages 21 - 65 years) were recruited to take part in a randomized, placebo controlled crossover design study. Subjects were screened to determine their health status (e.g. height, weight, body mass index, blood pressure and medical history). Subjects were randomly assigned to a sequence of two treatments with two study periods. The treatments are frozen wild blueberries and a placebo developed to match calories and fiber of the frozen wild blueberries. The subjects were asked to avoid high polyphenol foods in their typical diet for 7 days and consume one of the two treatments as a dietary intervention. After the seventh day subjects consumed a test meal along with either the wild blueberry or placebo. Blood was collected to determine glucose and satiety hormone levels.

Interventions

Blueberry - 150 grams wild blueberries (whole fruit)

OTHERPlacebo

Placebo - matched for calories and fiber

Sponsors

University of Prince Edward Island
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Male or female

Exclusion criteria

* BMI \< 20 and \> 30 kg/m² * Pregnant women or women who plan on becoming pregnant during the study * Postpartum women * Lactating women * Diabetes Mellitus * Kidney disease * Liver disease * GI Disease * Certain cancers * Smokers * Blueberry allergies

Design outcomes

Primary

MeasureTime frameDescription
Glucose (mmol/L)Change from baseline 0 hours and 2 hoursPlasma glucose

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026