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N/A N=55 Randomized Triple-blind Treatment

Blueberry Consumption and Type 2 Diabetes

Type2 Diabetes

Enrolled (actual)
55
Serious AEs
0.0%
Results posted
Apr 2022
Primary outcome: Primary: Blood Pressure — 125.6; 126.0; 74.6; 75.1 mm Hg — p=0.56

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Blueberry (Other); Placebo (Other)
Age
Adult, Older Adult · 45+ yrs
Sex
Male
Sponsor
Albany Research Institute, Inc.
Primary completion
Jun 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Blood Pressure
125.6; 126.0; 74.6; 75.1 0.56
SECONDARY
Hemoglobin A1C
7.1; 7.5 0.03 sig

Summary

Lifestyle strategies that include dietary modification, such as consumption of a plant-based diet, are well recognized in disease prevention and may improve type 2 diabetes. Various components of a plant-based diet may contribute to its beneficial health effects, but there has been keen interest in the possibility that plant polyphenols may have a role. Blueberries are dietary sources of polyphenols, specifically anthocyanins. To date there are few human clinical trials evaluating the beneficial health effects of blueberries in populations with type 2 diabetes. The objective of the study is to determine if freeze-dried blueberries compared to a blueberry placebo will improve cardiometabolic parameters in men with type 2 diabetes.

Eligibility Criteria

Inclusion Criteria

  • Male
  • Ages 45 to 75 years at beginning of study
  • BMI >25 kg/m2
  • HbA1C > 6.5 and 10% of body weight over the last 6 months; routine participation in heavy exercise
  • Heavy smokers (>20 cigarettes per day)
  • Unable or unwilling to give informed consent or communicate with study staff
  • Other medical, psychiatric, or behavioral factors that in the judgment of the Principal Investigators may interfere with study participation or the ability to follow the intervention protocol
  • Allergies to blueberries or blueberry products
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02972996). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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