Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
All Genders
ID06588218

Effect of Daily Fresh Watermelon Consumption on Gut and Cardiometabolic Health in Young Adults With Overweight and Obesity

Led by Florida State University · Updated on 2026-04-09

36

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the effect of daily fresh watermelon consumption over six weeks on gut health and cardiometabolic measures in young adults who are overweight or have obesity. It focuses on whether eating fresh watermelon can improve intestinal barrier health, increase beneficial gut bacteria diversity, and positively affect body composition, blood pressure, blood vessel function, blood lipid levels, and inflammation compared to a control snack. Participants will be randomly assigned to either consume about 2.5 cups of fresh watermelon daily or an isocaloric control snack consisting of a Belvita breakfast sandwich plus 12 ounces of water, both for six weeks. Both groups maintain their normal diet alongside these supplements. The study includes multiple visits for assessments during and after the intervention period. Participants will undergo evaluations at baseline, 6 weeks, 10 weeks, and 16 weeks, including tests of gut and oral microbiome diversity, gut transit time, arterial stiffness, endothelial function, blood pressure, body measurements, body composition, dietary intake, and various blood biomarkers related to inflammation, appetite, intestinal barrier function, and cardiometabolic health. The study monitors changes over time to understand the impact of watermelon consumption on these health aspects.

CONDITIONS

Brief Title

Effect of Watermelon on Gut and Cardiometabolic Health

Who Can Participate

Age: 18Years - 30Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Between 18 and 30 years old
  • Ability to speak and read in English
  • Overweight or Obese Class 1 and 2 (BMI 65 25 - 39.9 kg/m2)
Not Eligible

You will not qualify if you...

  • Intake of antibiotics in the last 3 months
  • Intake of pre/pro/postbiotics in the last 3 months
  • Current or past (within the last 6 months) user of tobacco, marijuana, or E-cigarette products
  • Cardiovascular disease (will not exclude for hypertension), gastrointestinal disease (ulcerative colitis, celiac, Crohn's disease, diverticulosis, peptic ulcers, small intestinal bacterial overgrowth, short bowel syndrome), neurological (multiple sclerosis, meningitis, recent stroke) or endocrine disorders (uncontrolled thyroid disorders, growth hormone disorders, adrenal gland disorders, uncontrolled diabetes - A1C greater than 9%)
  • Food allergy to study foods
  • Any allergy to melon
  • Any allergy to the isocaloric snack (gluten)
  • Regular consumption of watermelon greater than 2 servings / week
  • Current heavy alcohol use (65 15 drinks / week for men, 65 8 drinks / week for women)
  • Class 3 Obesity (BMI > 40 kg/m2)
  • Current user of Citrulline, Arginine, Nitric Oxide or other supplements known to affect nitric oxide synthesis (beet root juice or any beet supplement, Pycnogenol / Pine bark extract)
  • Known to be currently pregnant (self-disclosed)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit

Treatment

Duration - 6 weeks per condition

Participants follow two diet conditions in a crossover design: one with daily fresh watermelon consumption and one with an isocaloric control snack, each lasting six weeks.

3 visits during each treatment period (at baseline, week 6, and week 10)

Follow-up

Duration - 6 weeks

Participants are monitored for changes in gut and cardiometabolic health after completing both diet conditions.

1 visit at week 16

Trial Site Locations

Total: 1 location

1

Florida State University - Gut Biome Lab

Tallahassee, Florida, United States, 32306

Actively Recruiting

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Research Team

R

Ravinder Nagpal, PhD

C

Cole Patoine, M.S

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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