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Bioavailability of Ration Items Containing Tart Cherry Extract

United States Army Research Institute of Environmental Medicine · NCT07063173

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 17–39 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
15
US sites recruiting
1
Study start
June 14, 2024
Record last updated
December 29, 2025

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

To determine how consuming food items containing shelf-stored tart cherry impacts your body's ability to absorb and use the compounds within tart cherry.

Being studied: Fruit Bar; Powdered Drink; Commercially available 100% tart cherry juice; Placebo beverage

Conditions: Bioavailability

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Active duty military personnel and civilians will be invited to participate in the study if they:
  • Are between the ages of 18 (or 17 for military personnel) and 39.
  • Are willing to participate in all study procedures and comply with all study instruction.
  • In good health as determined by OMSO (Office of Medical Support and Oversight).
  • Supervisor approval for federal civilian employees and non-HRV active-duty military personnel stationed at NSSC

Exclusion Criteria

  • • Unable to understand verbal or written instructions or testing materials in English.
  • Have a bleeding disorder (e.g., von Willebrand Disease, hemophilia) or are being treated with medication that will impair blood clotting (for example, coumadin)
  • Have a history of GI-related conditions that may impact macronutrient absorption (e.g., Crohn's disease, ulcerative colitis, Celiac's disease or gluten sensitivity, bariatric surgery or gastroparesis, short bowel, inflammatory bowel disease, etc…);
  • Any use of antibiotics or antifungal, except topical antibiotics/antifungals within 3 months of study participation.
  • Colonoscopy within 3 months of study participation.
  • Regular (i.e., weekly or more frequent) use of over-the-counter medications (including antacids, laxatives, stool softeners, and antidiarrheals) unless approved by OMSO and study PI.
  • Are habitually taking nonsteroidal anti-inflammatory drugs (e.g., Advil, aspirin), corticosteroids (e.g., prednisone) or immunosuppressants (e.g. Humira);
  • Have an allergy or aversion (extreme dislike) to any of the test foods(e.g., cherry flavored beverages or bar). Allergy symptoms may include anaphylaxis, hives or eczema, tingling/itching in the mouth, dizziness or fainting, diarrhea, nausea or vomiting, swelling of the lips, face, tongue and throat).
  • Have donated blood within the past 8 weeks of the first test session or plan to donate blood during the study.
  • Are not willing to abstain from tobacco products and vigorous exercise for at least 24 hours" before each trial and consume a low-polyphenol diet two days prior to each test session and on the day of the test session.

Recruiting US locations

  • USARIEM

    Natick, MA 01760

    Site contact: Tracey J Smith, PhD · 508-206-2390 · treacey.smith10.civ@health.mil

Study contacts (from the official record)

  • Tracey J Smith, PhD · 5082062390 · tracey.smith10.civ@health.mil
  • Robert Roussel, PhD · robert.r.roussel.civ@health.mil
Bioavailability of Ration Items Containing Tart Cherry Extract (NCT07063173) | Bored Studies