Fruit and Vegetable Biomarker Discovery (UCD-DBDC)

May 27, 2026 updated by: University of California, Davis

University of California (UC), Davis Dietary Biomarkers Development Center

The purpose of this research is to find a set of markers in the blood and/or urine that can be linked to consumption of specific fruits and vegetables. This will allow for better understanding of the link between diet and health-related outcomes. Furthermore, the results of this study will lead to the development of new methods to evaluate the nutritional status of individuals in both community and clinical settings. Food frequency questionnaires and diaries/recalls can be affected by intentional or unintentional misreporting, and thus can create errors in determining nutritional status. This study will lead to the development of an objective way to assess the consumption of specific fruits and vegetables by the general population.

Study Overview

Detailed Description

The purpose of this research is to find a set of markers in the blood and/or urine that can be linked to consumption of specific fruits and vegetables. This will allow for better understanding of the link between diet and health-related outcomes. Furthermore, the results of this study will lead to the development of new methods to evaluate the nutritional status of individuals in both community and clinical settings. Food frequency questionnaires and diaries/recalls can be affected by intentional or unintentional misreporting, and thus can create errors in determining nutritional status. This study will lead to the development of an objective way to assess the consumption of specific fruits and vegetables by the general population.

This study includes 3 aims to identify and then validate urine and plasma biomarkers associated with fruit and vegetable intake. Aim 1 will use a randomized crossover dietary intervention to determine the dose and time response of metabolites in plasma and urine associated with exposure to a mixture of MyPlate fruits and vegetables. Aim 2 will use a parallel design, controlled diet intervention to determine whether the biomarkers of fruit and vegetable intake determined in Aim 1 are predictors of consumption in the context of a defined dietary pattern. Aim 3 will be a cross-sectional validation arm that determines if the biomarkers of food intake developed in Aims 1 and 2 have predictive value reflecting recent and habitual consumption of these foods in a heterogeneous and diverse population.

Study Type

Interventional

Enrollment (Actual)

300

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Davis, California, United States, 95616
        • USDA ARS Western Human Nutrition Research Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Body Mass Index (BMI) 18.5-39.9 kg/m^2
  • Willingness to provide urine and have blood drawn

Exclusion Criteria:

  • Pregnancy or lactation
  • Allergy or aversion to foods provided in test diet
  • History of gastrointestinal disorders including the following:

    1. Ulcerative colitis or Crohn's disease
    2. Celiac sprue
    3. Hereditary non-polyposis colorectal cancer (HNPCC)
    4. Familial adenomatous polyposis
    5. Pancreatic disease
    6. Liver disease
  • Previous gastrointestinal resection or bariatric surgery
  • Bleeding disorders that preclude blood draws
  • Recent hospital admissions (past 6 months) for myocardial infarction (MI), cerebrovascular accident (CVA), or congestive heart failure (CHF)
  • Cardiovascular disease (CVD) under physician guided therapy that is not medically stable
  • Cancer under radiation or chemotherapy treatment that is active or within 6 months of treatment
  • Weight change (± 5% in the last 3 months)
  • Regular alcohol intake of > 2 drinks/day (equivalent to 720 mL of beer, 240 mL of wine, or 90 mL of spirits), and unwilling to abstain during feeding periods
  • Use of tobacco and/or marijuana, hookahs, e-cigarettes, or vapes and not willing to abstain during feeding periods
  • Use of illicit drugs and not willing to abstain during feeding periods
  • BMI >40 kg/m^2
  • Regular (daily to weekly) use of over-the-counter (OTC) weight-loss aids and unwilling or unable to stop taking these during feeding periods
  • Regular (daily to weekly) use of OTC anti-inflammatories and unwilling or unable to stop taking these during feeding periods
  • Unwilling to stop taking OTC dietary supplements that interfere with the test foods being studied including pills, chewables, liquids or powders for the following (may continue if vitamin supplement is prescribed by a medical doctor):

    1. Protein supplements
    2. Soy
    3. Fiber
    4. Flaxseed
    5. Fish oil (including cod liver oil)
    6. Probiotics
    7. Carotenoids
    8. Selenium
    9. Other antioxidants
    10. Other phytochemicals
    11. Glucosamine
    12. Chondroitin
  • Oral or IV antibiotic use in the past 6 months (could defer participation until 6 months post-completion of course of antibiotics)
  • Seated blood pressure >140/90 mmHg
  • Fasting clinical lab values outside of the following ranges:

    1. Fasting Glucose: 54-125 mg/dL
    2. Urea: 6-50 mg/dL
    3. Creatinine: 0.4-1.3 mg/dL
    4. Estimated Glomerular Filtration Rate (eGFR): >60 mL/min
    5. Sodium: 133-146 mmol/L
    6. Alanine Transaminase (ALT): 5-60 U/L
    7. Aspartate Aminotransferase (AST): 5-40 U/L
    8. Alkaline Phosphatase (ALP): 20-135 U/L
    9. Total Bilirubin: 0.0-1.9 mg/dL
    10. Total Protein: 5-9.0 g/dL
    11. Albumin: 3.5-5.9 d/L
    12. Low-density Lipoprotein (LDL) Cholesterol: <160 mg/dL
    13. Triglycerides: <500
    14. White Blood Cells: 3-10.5 Kl/µL
    15. Hematocrit: 35-48 g/dL (women), 37.5-49 g/dL (men)
  • Current use of the following prescription medications:

    1. Diuretics
    2. Steroids (oral): daily oral any dose within 1 month of study (except for oral contraceptive pills)
    3. Opiates: any use within 1 month of study
    4. Hypolipidemic agents that affect GI or renal function (ie. fibrates)
    5. Hypoglycemic medications other than metformin (ie. insulin, SGLT2 inhibitor, α-glucosidase inhibitor)
    6. Psychiatric medications that affect metabolism/renal function (anti-psychotics, lithium)
    7. Biologics/immune modulators (ie. rheumatoid arthritis, psoriasis, other rheumatologic/hematologic active disease)
    8. Anti-coagulants (coumadin, heparin, Eliquis, etc.)
    9. HIV/HAART medications (dyslipidemia inducing)
  • Inability to freely give informed consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Non-Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Aim 1 Group 1

Order of Treatments:

Meal Challenge 1, Meal Challenge 2, Meal Challenge 3

A meal challenge will be provided that contains 1 serving of peaches and 2 servings of strawberries as a smoothie and 2 servings of tomatoes and 1 serving of carrot as a vegetable dish.
A meal challenge will be provided that contains 1 serving of banana and 2 servings of peaches as a smoothie and 1 serving of tomatoes and 2 servings of green beans as a vegetable dish.
A meal challenge will be provided that contains 2 serving of bananas and 1 serving of strawberries as a smoothie and 1 serving of green beans and 2 servings of carrots as a vegetable dish.
Experimental: Aim 1 Group 2

Order of Treatments:

Meal Challenge 1, Meal Challenge 3, Meal Challenge 2

A meal challenge will be provided that contains 1 serving of peaches and 2 servings of strawberries as a smoothie and 2 servings of tomatoes and 1 serving of carrot as a vegetable dish.
A meal challenge will be provided that contains 1 serving of banana and 2 servings of peaches as a smoothie and 1 serving of tomatoes and 2 servings of green beans as a vegetable dish.
A meal challenge will be provided that contains 2 serving of bananas and 1 serving of strawberries as a smoothie and 1 serving of green beans and 2 servings of carrots as a vegetable dish.
Experimental: Aim 1 Group 3

Order of Treatments:

Meal Challenge 2, Meal Challenge 3, Meal Challenge 1

A meal challenge will be provided that contains 1 serving of peaches and 2 servings of strawberries as a smoothie and 2 servings of tomatoes and 1 serving of carrot as a vegetable dish.
A meal challenge will be provided that contains 1 serving of banana and 2 servings of peaches as a smoothie and 1 serving of tomatoes and 2 servings of green beans as a vegetable dish.
A meal challenge will be provided that contains 2 serving of bananas and 1 serving of strawberries as a smoothie and 1 serving of green beans and 2 servings of carrots as a vegetable dish.
Experimental: Aim 1 Group 4

Order of Treatments:

Meal Challenge 2, Meal Challenge 1, Meal Challenge 3

A meal challenge will be provided that contains 1 serving of peaches and 2 servings of strawberries as a smoothie and 2 servings of tomatoes and 1 serving of carrot as a vegetable dish.
A meal challenge will be provided that contains 1 serving of banana and 2 servings of peaches as a smoothie and 1 serving of tomatoes and 2 servings of green beans as a vegetable dish.
A meal challenge will be provided that contains 2 serving of bananas and 1 serving of strawberries as a smoothie and 1 serving of green beans and 2 servings of carrots as a vegetable dish.
Experimental: Aim 1 Group 5

Order of Treatments:

Meal Challenge 3, Meal Challenge 1, Meal Challenge 2

A meal challenge will be provided that contains 1 serving of peaches and 2 servings of strawberries as a smoothie and 2 servings of tomatoes and 1 serving of carrot as a vegetable dish.
A meal challenge will be provided that contains 1 serving of banana and 2 servings of peaches as a smoothie and 1 serving of tomatoes and 2 servings of green beans as a vegetable dish.
A meal challenge will be provided that contains 2 serving of bananas and 1 serving of strawberries as a smoothie and 1 serving of green beans and 2 servings of carrots as a vegetable dish.
Experimental: Aim 1 Group 6

Order of Treatments:

Meal Challenge 3, Meal Challenge 2, Meal Challenge 1

A meal challenge will be provided that contains 1 serving of peaches and 2 servings of strawberries as a smoothie and 2 servings of tomatoes and 1 serving of carrot as a vegetable dish.
A meal challenge will be provided that contains 1 serving of banana and 2 servings of peaches as a smoothie and 1 serving of tomatoes and 2 servings of green beans as a vegetable dish.
A meal challenge will be provided that contains 2 serving of bananas and 1 serving of strawberries as a smoothie and 1 serving of green beans and 2 servings of carrots as a vegetable dish.
Experimental: Aim 2 Typical American Diet
The diet will provide sufficient calories for weight maintenance and will contain refined grains and low amounts of fruits and vegetables, representative of the typical American diet. No bananas, strawberries, peaches, green beans, carrots, or tomatoes will be provided.
Experimental: Aim 2 Typical American Diet Plus Test Foods
This diet will provide sufficient calories for weight maintenance and will contain refined grains and low amounts of fruits and vegetables, representative of the typical American diet. Bananas, strawberries, peaches, green beans, carrots, and tomatoes will be provided in amounts less than or equal to 1 serving per day each.
Experimental: Aim 2 Dietary Guidelines for Americans Diet Plus Test Foods
This diet will provide sufficient calories for weight maintenance and will contain whole grains and high amounts of fruits and vegetables, representative of the Dietary Guidelines for Americans. Bananas, strawberries, peaches, green beans, carrots, and tomatoes will be provided in amounts greater than or equal to 1 serving per day each.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in urine metabolomics profile
Time Frame: Aim 1: day 3, 8, 13; overnight fasted and post prandial 0-2 hours, 2-4 hours, 4-6 hours, 6-8 hours, 8-24 hours. Aim 2: day 3, 9, 10; Aim 3: day 4.
Urine metabolites will be measured by ultra-performance liquid chromatography mass spectrometry (UPLC-MS) before and after consumption of no, low, or high doses of study fruits and vegetables. Change will be assessed by the appearance of and change in levels of dietary-derived metabolites, which are candidate dietary biomarkers.
Aim 1: day 3, 8, 13; overnight fasted and post prandial 0-2 hours, 2-4 hours, 4-6 hours, 6-8 hours, 8-24 hours. Aim 2: day 3, 9, 10; Aim 3: day 4.
Change in plasma metabolomics profile
Time Frame: Aim 1: day 3, 8, 13; overnight fasted and post prandial 1 hour, 2 hour, 3 hour, 4 hour, 5 hour, 6 hour, 7 hour, 8 hour, 24 hour. Aim 2: days 3, 9, 10. Aim 3: day 4.
Plasma metabolites will be measured by ultra-performance liquid chromatography mass spectrometry (UPLC-MS) before and after consumption of no, low, or high doses of study fruits and vegetables. Change will be assessed by the appearance of and change in levels of dietary-derived metabolites, which are candidate dietary biomarkers.
Aim 1: day 3, 8, 13; overnight fasted and post prandial 1 hour, 2 hour, 3 hour, 4 hour, 5 hour, 6 hour, 7 hour, 8 hour, 24 hour. Aim 2: days 3, 9, 10. Aim 3: day 4.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diet adherence
Time Frame: Aim 1: day 3, 8, 13. Aim 2: day 3, 6, and 9.
Intake of test and non-test meals/foods will be monitored through weigh-backs by study personnel in Aim 1 and participant self report in Aim 2 to identify deviations in intake of fruits/vegetables of interest.
Aim 1: day 3, 8, 13. Aim 2: day 3, 6, and 9.
Habitual consumption of fruits and vegetables
Time Frame: Day 1
3-month General Nutrition Assessment Food Frequency Questionnaires (GNA FFQ) will be administered at site visit 1 for each aim.
Day 1
Acute consumption of fruits and vegetables
Time Frame: Days 1, 2, 3.
An Automated Self-Administered 24-Hour (ASA24) 3-day food record will be obtained over 2 weekdays and 1 weekend day during Aim 3.
Days 1, 2, 3.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Carolyn M Slupsky, PhD, University of California, Davis

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2023

Primary Completion (Actual)

March 13, 2026

Study Completion (Actual)

March 13, 2026

Study Registration Dates

First Submitted

November 10, 2022

First Submitted That Met QC Criteria

November 10, 2022

First Posted (Actual)

November 18, 2022

Study Record Updates

Last Update Posted (Actual)

May 29, 2026

Last Update Submitted That Met QC Criteria

May 27, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 1788772
  • 2021-67017-35783 (Other Grant/Funding Number: USDA)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All individual participant data (IPD) will be sent to the Data Coordinating Center (DCC) at Duke University. The DCC will make study data available to other Consortium members, including researchers at Fred Hutchinson Cancer Center and Harvard, and their affiliates in accordance with best practices for data safety and accessibility. The data may be stored and shared for future research without additional informed consent provided all identifiable private information, such as the subject's name or other identifying information are removed. Once identifying information is removed from the data, we will no longer be able to identify and destroy data belonging to participants who wish to remove their samples from future research. The final de-identified study data and results will be made publicly available, in accordance with National Institutes of Health (NIH) data sharing policies.

IPD Sharing Time Frame

Data will be embargoed until publications are complete, at which time they will be made available to the scientific community.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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