RecruitingNot ApplicableNCT06672952

Dose-Response Impact of Glucosyl-Hesperidin (CitraPeak) on Exercise Performance, Blood Flow, Stress, Cognition, and Other Perceptual Indicators


Sponsor

Lindenwood University

Enrollment

60 participants

Start Date

Apr 15, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the dose-dependent effects of glucosyl-hesperidin (CITRAPEAK) supplementation on exercise performance, recovery indicators, blood flow, cognitive function, mood, sleep, and fuel utilization in recreationally active adults.


Eligibility

Min Age: 18 YearsMax Age: 50 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying 200 mg CITRAPEAK® (glucosyl-hesperidin) supplementation, 400 mg CITRAPEAK® (glucosyl-hesperidin) supplementation, and others for people with blood flow, cognitive function, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 50 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENT400 mg CITRAPEAK® (glucosyl-hesperidin) supplementation

The active intervention consists of 400 mg of glucosyl-hesperidin (CITRAPEAK®) in capsule form.

DIETARY_SUPPLEMENTPlacebo

The placebo intervention consists of 400 mg/day of cellulose in capsule form, matching the appearance and dosage of active interventions.

DIETARY_SUPPLEMENT200 mg CITRAPEAK® (glucosyl-hesperidin) supplementation

The active intervention includes 200 mg of glucosyl-hesperidin (CITRAPEAK®) and an additional 200 mg of cellulose in capsule form.


Locations(1)

Lindenwood University

Saint Charles, Missouri, United States

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NCT06672952


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