NCT07298863 The Effect of Hydration Status on Substrate Oxidation at Rest and During Light and Moderate Exercise
| NCT ID | NCT07298863 |
| Status | Recruiting |
| Phase | — |
| Sponsor | PepsiCo Global R&D |
| Condition | Hydration Status |
| Study Type | INTERVENTIONAL |
| Enrollment | 74 participants |
| Start Date | 2025-11-05 |
| Primary Completion | 2026-04-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 74 participants in total. It began in 2025-11-05 with a primary completion date of 2026-04-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Metabolic flexibility is the ability to properly switch between fat and carbohydrate stores to use for energy under different conditions (rest, feeding, exercise). Impairments in metabolic flexibility, also known as metabolic inflexibility, have been suggested to be an underlying cause of metabolic disease, like type 2 diabetes. Long-term low fluid intake may increase the risk of type 2 diabetes due to insulin resistance, a form of metabolic inflexibility. Further, low fluid intake has been shown to impair the ability to switch fuel preference during exercise. While there is some evidence that low fluid intake may lead to impaired metabolic flexibility, more information is needed. Therefore, the purpose of this study is to evaluate the impact of hydration status on substrate preference at rest and during exercise at varying intensities (light and moderate). Further, we will examine whether biological sex and menstrual cycle phase impact hydration and metabolism under these same conditions.
Eligibility Criteria
Inclusion Criteria: * Subject is male or female * If female, subject is not pregnant (based on self-report) * If female, subject has stopped taking birth control medication or removed long-acting reversible contraceptive \>6 months at start of the study * If female, subject has normal menstrual cycle (21-35 days) * If female, subject is willing to track their menstrual cycle * If female, subject has a smartphone compatible for application to track menstrual cycle (female only) and/or wearable data (females and males) * Subject is 18-35 years of age, inclusive * Subject body mass index (BMI) is between 18.5-25 kg/m2 * Subject is at least recreationally active (engaged in moderate-intensity, intermittent, or steady-state exercise at least 3 days per week for at least 60 min at a time) * Subject is accustomed to cycling for at least 60 min * Subject does not smoke (or has quit for at least 6 months) * Subject is not taking medication that may interfere with the study (e.g., diuretics, laxatives, or weight loss drugs) * Subject has no health conditions that would interfere with the study as indicated on the general health questionnaire (GHQ) e.g. cardiovascular, renal, or metabolic diseases * Subject is not actively involved in weight loss intervention (dieting and/or anti-obesity medications) * Subject is not allergic to adhesives (e.g., medical tape) * Subject is willing to avoid alcohol consumption 24 hours prior to visit(s) * Subject is willing to fast overnight (\~8-12 hours) * Subject is willing to refrain from vigorous exercise for 24 hours (light physical activity only) * Subject is willing to be shaved at patch or electrode site, if necessary * Subject is willing to eat the exact same food the day prior to each visit to the laboratory * Able to speak, write, and read English * Provision of written consent to participate Exclusion Criteria: * Subject has participated in a clinical trial within the past 30 days * Subject has participated in any PepsiCo trial within past 36 months * Subject has a condition or is taking medication that the investigator believes would interfere with his/her ability to provide informed consent, comply with the study protocol, which might confound the interpretation of the study results, or put the person at undue risk * Subject is allergic to alcohol (alcohol pre pads are used for blood draws * If female, subject is taking birth control medication or has long-acting reversible contraceptive * If male, subject is undergoing hormone therapy to alter testosterone levels (injections, transdermal patch, pill, etc.) * Subject is employed by, or has a parent, guardian, or other immediate family member employed by a company that manufactures any products that compete with any Gatorade product. If subject is unsure if a company would be considered a competitor to Gatorade, they will be asked to please let the study investigator know the name of the other company and the nature of their relationship to that company before they sign the informed consent.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07298863 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 35 Years, studying Hydration Status. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07298863 currently recruiting?
Yes, NCT07298863 is actively recruiting participants. Contact the research team at GSSIresearchstaff@pepsico.com for enrollment information.
Where is the NCT07298863 trial being conducted?
This trial is being conducted at Valhalla, United States.
Who is sponsoring the NCT07298863 clinical trial?
NCT07298863 is sponsored by PepsiCo Global R&D. The trial plans to enroll 74 participants.