To Determine the Metabolomics and Microbiome Changes After Cranberry Juice Consumption Among Young Women
Completed · Not applicable · Has a placebo group
Conditions studied: Healthy
In brief
The compliance of participants in cranberry related clinical trial is poor due to the bitterness and astringency of cranberry products. There is a pressing need for an effective approach to verify participant compliance. The PLS-DA (Partial Least Squares Discriminant Analysis) /OPLS-DA (Orthogonal Partial Least Squares Discriminant Analysis) models established from the investigator's previous study provide an opportunity to identify cranberry juice consumers. In this blinded, placebo-controlled, cross-over study, investigators hypothesize that the established statistical models of PLS-DA (Partial least squares discriminant analysis) /OPLS-DA (Orthogonal partial least squares discriminant analysis) can identify cranberry juice consumers and non-consumers by analyzing the metabolomic changes in blood and urine among young women. In order to further explore the function of cranberry, microbiome profile will also be compared between cranberry juice consumption and placebo consumption after long-term treatment. Another comparison of metabolomic changes between short-term treatment and long-term treatment will be made to further identify candidate biomarkers of cranberry consumption and explore the correlation between acute effects and chronic effects of cranberry.
Key facts
- Study ID
- NCT02860468
- Run by
- University of Florida
- People needed
- 21
- Starts
- 2017-01-16
- Expected to finish
- 2018-11-15
- Last updated by the study team
- 2018-11-16
Who can join
Age: 18 and older, up to 29. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Healthy
- Normal BMI (18.5-25)
- Body weight ≥110 pounds
You may not qualify if…
- Gastrointestinal disorders
- Urological diseases
- Metabolic disorders
- Smokers
- Pregnancy
- Previous use of antibiotics or probiotics.
Where it is running
- Food Science and human nutrition department at University of Florida — Gainesville, Florida, United States
Full record on ClinicalTrials.gov
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