Actively Recruiting
Postprandial Response to Fruit Juice
Led by Ocean Spray Cranberries, Inc. · Updated on 2025-08-05
18
Participants Needed
1
Research Sites
14 weeks
Total Duration
On this page
Sponsors
O
Ocean Spray Cranberries, Inc.
Lead Sponsor
B
Biofortis Innovation Services
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to determine postprandial responses to fruit juices.
CONDITIONS
Official Title
Postprandial Response to Fruit Juice
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between 18 and 45 years of age at first visit
- Body mass index (BMI) between 18.5 and less than 30.0 kg/m2 at first visit
- Fasting capillary glucose of 110 mg/dL or less at first visit
- Willing to avoid high-polyphenol foods for 48 hours before each test visit
- Willing to abstain from alcohol for 24 hours before each study visit
- No use of tobacco or nicotine products in the 12 months before first visit and no plans to start during the study
- Not a daily or almost daily user of marijuana or hemp products and willing to abstain throughout the study (topical creams allowed)
- Willing to maintain usual physical activity during the study
- Willing to maintain usual diet and stable intake of vitamins, minerals, supplements, and medications not interfering with outcomes
- Vein Access Scale score of 7 to 10 at first visit
- No health conditions preventing study participation as judged by the Clinical Investigator
- Understands study procedures and consents to participate and release of health information
You will not qualify if you...
- History or presence of serious cardiac, renal, hepatic, endocrine, pulmonary, biliary, pancreatic, gastrointestinal, or neurological disorders affecting study adherence or outcomes
- Uncontrolled high blood pressure (systolic ≥140 mm Hg or diastolic ≥90 mm Hg) at first visit
- Unstable use of antihypertensive medications within 30 days before first visit
- Unstable use of thyroid hormone replacement within 30 days before first visit
- Use of medications or supplements affecting carbohydrate metabolism within 30 days before first visit
- Extreme dietary habits (e.g., ketogenic, very high protein, very high fiber, vegan, vegetarian) as judged by Clinical Investigator
- Weight change over 4.5 kg in 60 days before first visit
- Current or planned weight loss regimen during study
- Use of weight loss medications within 90 days before first visit
- History of weight-reducing gastrointestinal surgery
- History of diagnosed eating disorders
- Known allergy or sensitivity to study beverage ingredients
- History of cancer in prior 2 years except non-melanoma skin cancer
- Major trauma or surgery within 60 days before first visit
- Blood donation over 450 mL within 60 days before second visit or planned donation during study
- Female who is pregnant, planning pregnancy, lactating, or with unstable use of sex hormones for contraception
- Recent or potential alcohol or substance abuse
- Exposure to non-registered drug products within 30 days before first visit
- Any condition that may interfere with consent or study compliance as judged by Clinical Investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Biofortis Innovation Services
Addison, Illinois, United States, 60101
Actively Recruiting
Research Team
K
Kristen S Smith, PhD, RD
CONTACT
C
Christina Khoo, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
6
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here