Short-term Health Effects of Wild Blueberry Juice Consumption

Pre-diabetes Clinical Trial

Official title:

Short-term Health Effects of Wild Blueberry Juice Consumption

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02139878
• Other study ID #: UPEI HS 01
• Status: Recruiting
• Phase: N/A
• First received: May 4, 2014
• Last updated: May 13, 2014
• Start date: May 2014
• Est. completion date: June 2014

Study information

• Verified date: May 2014
• Source: University of Prince Edward Island
• Contact: Kim Stote, PhD, MPH, RD
• Phone: 902 894-2890
• Email: kstote[@]upei.ca
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

Researchers at the University of Prince Edward Island want to learn about the health effects of wild blueberry juice.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: June 2014
• Est. primary completion date: June 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 25 Years to 65 Years

Eligibility

Inclusion Criteria:

• Healthy individuals at risk for type 2 diabetes

Exclusion Criteria:

• have a body mass index of less than 20 and greater than 45 kg/m2.

• are less than 21 and greater than 65 years old at beginning of study

• have smoked or used tobacco within 6 months prior to the start of the study

• are pregnant, plan to become pregnant or become pregnant during the study

• have a history or presence of kidney disease, liver disease, certain cancers, gastrointestinal, other metabolic diseases, or malabsorption syndromes

• have type 2 diabetes and need to use oral diabetic drugs or insulin

• have an allergy or adverse reaction to blueberries

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject)

Related Conditions & MeSH terms

• Pre-diabetes

Intervention

Other:
• Wild blueberry juice

• Placebo wild blueberry juice

Locations

Country	Name	City	State
Canada	University of Prince Edward Island, Health Sciences	Charlottetown	Prince Edward Island

Sponsors (1)

Lead Sponsor	Collaborator
University of Prince Edward Island

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Oxidative stress		Up to 4 weeks	No
Secondary	Glucose regulation		Up to 4 weeks	No