Actively Recruiting

Phase Not Applicable
Age: 17Years - 39Years
All Genders
Healthy Volunteers
ID07063173

Bioavailability of Ration Items Containing Tart Cherry Extract

Led by United States Army Research Institute of Environmental Medicine · Updated on 2025-12-29

15

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand how eating shelf-stored tart cherry products affects the body's ability to absorb and use compounds found in tart cherries. Researchers are studying this because tart cherry products may help reduce muscle damage and soreness and improve antioxidant capacity after exercise. The study involves active-duty military personnel and civilians aged 17 to 39 who are in good health and willing to follow study instructions. Participants will take part in a randomized, crossover study where they consume four different food products over four sessions with five-day breaks between them. These products include a commercial tart cherry juice, a snack bar with tart cherry powder, a powdered drink with tart cherry powder, and a control beverage without tart cherry. Each tart cherry product contains about 120 mg of anthocyanins, a key compound being studied. During each session, participants will fast overnight, have an IV catheter placed for blood sampling before and after consuming the product, and provide urine samples. Blood and urine will be tested for polyphenol levels and antioxidant markers at multiple time points up to 24 hours. The study will also explore links between the results and gut microbiome composition. Participation includes four sessions with detailed monitoring, and the study plans to collect complete data from up to 15 participants.

CONDITIONS

Brief Title

Bioavailability of Ration Items Containing Tart Cherry Extract

Who Can Participate

Age: 17Years - 39Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Active duty military personnel or civilians aged 18 to 39 (17 allowed for military personnel)
  • Willing to participate in all study procedures and follow study instructions
  • In good health as confirmed by medical support office
  • Supervisor approval required for federal civilian employees and certain military personnel
Not Eligible

You will not qualify if you...

  • Unable to understand instructions or testing materials in English
  • Have bleeding disorders or take blood clotting medications
  • History of gastrointestinal conditions affecting nutrient absorption
  • Use of antibiotics or antifungal medications (except topical) within 3 months
  • Underwent colonoscopy within 3 months
  • Regular use of certain over-the-counter medications unless approved
  • Habitual use of nonsteroidal anti-inflammatory drugs, corticosteroids, or immunosuppressants
  • Allergy or strong dislike to test foods, including cherry-flavored products
  • Donated blood within 8 weeks before first test session or plan to donate during study
  • Unwilling to avoid tobacco and vigorous exercise 24 hours before each trial and follow a low-polyphenol diet before sessions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 sessions with 5-day washout periods in between each

Participants consume four different food products containing tart cherry components and a control item over four separate sessions with a five-day washout period between each session. On each session day, blood samples are collected before and after consumption to measure polyphenol concentrations and antioxidant capacity.

4 in-person visits for experimental sessions plus blood sample collections on the day of and the day after each session

Trial Site Locations

Total: 1 location

1

USARIEM

Natick, Massachusetts, United States, 01760

Actively Recruiting

Loading map...

Research Team

T

Tracey J Smith, PhD

R

Robert Roussel, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

OTHER

Number of Arms

4

Similar Trials

Evaluating Kinetics and Bioavailability of Aronia Melanocarp...

Bioavailability

Actively Recruiting

1 location

Curcumin and Retinal Amyloid-beta Pilot Study

Bioavailability

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

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