Mango Intake and Gut and Cardiometabolic Health in Hispanic/Latino Adolescents
NCT ID: NCT07125001
Last Updated: 2026-02-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
25 participants
INTERVENTIONAL
2025-10-01
2028-03-31
Brief Summary
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Detailed Description
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Twenty-five (12-19 years of age) adolescents will be enrolled in a randomized, controlled 2-arm crossover dietary intervention trial. Participants will be randomized to consume either ¾ cups of mango or continue their habitual diet for 4 weeks, followed by a 4-week washout period before crossing over to the alternate group. The mango flesh will be cut into uniform chunks (2-3 cm) and portioned into individual servings that can be consumed either as-is or blended into a smoothie.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Mango arm
Ataulfo Mango intake
Ataulfo mango
4 weeks of Ataulfo mango intake
No mango intake
4 weeks of no mango intake
No interventions assigned to this group
Interventions
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Ataulfo mango
4 weeks of Ataulfo mango intake
Eligibility Criteria
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Inclusion Criteria
* BMI ≥ 85th percentile (https://www.bcm.edu/bodycomplab/BMIapp/BMI-calculator-kids.html)
* Self-reported Hispanic/Latino
* Subject is willing and able to comply with the study protocols
* Subject is willing to consume the test products
* Female-specific criteria: if menstruating, eumenorrheic (regular monthly menstrual cycles of 25-30-days in length)
* Access to a smartphone or tablet at least 1x / day and willing to take pictures associated with the products to be consumed in the study
Exclusion Criteria
* Currently taking prescription drugs, with the exception of asthma inhalers, which are allowed
* BMI \<85th percentile (https://www.bcm.edu/bodycomplab/BMIapp/BMI-calculator-kids.html)
* Current participation in a moderate or high-intensity daily exercise routine
* Self-reported disease, serious illness, or who are currently under acute medical care.
* Currently taking prescription drugs.
* Any supplement use, including multi-vitamin/ mineral, herbal, plant or botanical, fish oil, and oil supplements, and not willing to discontinue before starting the study.
* Vegetarian or vegan diet
* Self-reported malabsorption or gastrointestinal issues
* Fruit and vegetable intake exceeding daily recommendations of 5 servings
* Smoking (vaping, conventional nicotine-containing products or marijuana)
* Current enrollee in a clinical research study
12 Years
19 Years
ALL
Yes
Sponsors
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University of California, Davis
OTHER
Responsible Party
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Principal Investigators
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Roberta R Holt, PhD
Role: PRINCIPAL_INVESTIGATOR
University of California, Davis
Locations
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Academic Surge; Ragle Human Nutrition Research Center
Davis, California, United States
Countries
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Central Contacts
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Facility Contacts
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Roberta R Associate Researcher, PhD
Role: primary
California
Role: backup
Other Identifiers
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1939453
Identifier Type: -
Identifier Source: org_study_id
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