- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06323070
Effects of Watermelon or Low-fat Cookie Consumption on Wellness
August 25, 2026 updated by: San Diego State University
The objective of the proposed research is to determine the effects of fresh watermelon consumption on physiological indicators of wellness regarding sexual, skin and gut health in adults.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
80
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 Contact
- Name: Mee Young Hong, PhD
- Phone Number: 619-594-2392
- Email: mhong2@sdsu.edu
Study Locations
-
-
California
-
San Diego, California, United States, 92182
- Recruiting
- School of Exercise and Nutritional Sciences
-
Contact:
- Mee Young Hong, PhD
- Phone Number: 619-594-2392
- Email: mhong2@sdsu.edu
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Generally healthy subjects
- BMI 20-40 kg/m2
Exclusion Criteria:
- Smoker
- Pregnant woman
- Required antibiotics use
- Required dietary supplement use
- Required medication of metabolic disorders, mental health and sexual health
- Allergy to watermelon or wheat
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: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Low-fat cookies
Subjects consume 100 kcal of low-fat cookies daily for 4 weeks.
|
To determine the effects of low-fat cookie consumption on physiological indicators of wellness regarding sexual, skin, and gut health
|
|
Experimental: Watermelon
Subjects consume 100 kcal of watermelon daily for 4 weeks.
|
To determine the effects of watermelon consumption on physiological indicators of wellness regarding sexual, skin, and gut health
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of sexual health questionnaire scores
Time Frame: Baseline and week 4
|
Change of sexual health questionnaire scores will be determined to examine effects of watermelon consumption vs low-fat cookies.
|
Baseline and week 4
|
|
Change of skin hydration scores
Time Frame: Baseline, 1 min post application and week 4 consumption
|
Change of skin hydration scores will be determined to examine effects of watermelon consumption vs low-fat cookies.
|
Baseline, 1 min post application and week 4 consumption
|
|
Change of microbiome diversity
Time Frame: Baseline and week 4
|
Change of microbiome diversity will be determined to examine effects of watermelon consumption vs low-fat cookies.
|
Baseline and week 4
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of depression questionnaire scores
Time Frame: Baseline and week 4
|
Change of depression questionnaire scores will be determined to examine effects of watermelon consumption vs low-fat cookies.
|
Baseline and week 4
|
|
Changes of trimethylamine N-oxide (TMAO) levels
Time Frame: Baseline and week 4
|
Changes in trimethylamine N-oxide (TMAO) levels will be determined to examine the effects of watermelon consumption vs low-fat cookies.
|
Baseline and week 4
|
|
Changes of cholesterol levels
Time Frame: Baseline and week 4
|
Changes in cholesterol levels will be determined to examine the effects of watermelon consumption vs low-fat cookies.
|
Baseline and week 4
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mee Young Hong, PhD, San Diego State University
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)
March 1, 2024
Primary Completion (Estimated)
December 1, 2028
Study Completion (Estimated)
December 1, 2028
Study Registration Dates
First Submitted
March 14, 2024
First Submitted That Met QC Criteria
March 14, 2024
First Posted (Actual)
March 21, 2024
Study Record Updates
Last Update Posted (Actual)
August 28, 2026
Last Update Submitted That Met QC Criteria
August 25, 2026
Last Verified
August 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HS-2023-0281
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.