COMPLETED

The Impact of KETO5 XOGenius Beverage on Markers of Physiological and Neurocognitive Health

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The primary objectives of this application are to 1) investigate the effect of increased daily consumption of the Keto5 XOGenius beverage on outcomes associated with elevated risk for various neurocognitive and pathophysiological conditions/diseases. And 2) to investigate the effect of daily consumption of the Keto5 XOGenius beverage on the following variables: waist circumference, body weight, and body mass index (BMI).

Official Title

The Impact of KETO5 XOGenius Beverage on Markers of Physiological and Neurocognitive Health

Quick Facts

Study Start:2023-08-01
Study Completion:2025-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06318390

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.

Ages Eligible for Study:18 Years to 50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Men and women who are between the ages of 18-50
  1. * Individuals who have donated more than 550 ml of blood within the past 8 weeks will not have blood drawn from them in this protocol. However, if they remain interested in the study, and otherwise meet the inclusion criteria, then we may still opt to proceed with data collection.
  2. * Food allergies
  3. * Type I diabetes/Type II diabetes, and/or a history of hypoglycemia.
  4. * History of irritable bowel syndrome or inflammatory bowel disease.
  5. * Currently taking any medications that are designed to treat a cardiovascular or metabolic condition
  6. * Pregnant women
  7. * Breast feeding women
  8. * Allergy to spandex/lycra/latex
  9. * Anemia
  10. * Use of prescription stimulants

Contacts and Locations

Principal Investigator

Robert M Brothers, PhD
PRINCIPAL_INVESTIGATOR
University of Texas at Arlington

Study Locations (Sites)

UT Arlington - Science and Engineering Innovation and Research Building
Arlington, Texas, 76019
United States

Collaborators and Investigators

Sponsor: The University of Texas at Arlington

  • Robert M Brothers, PhD, PRINCIPAL_INVESTIGATOR, University of Texas at Arlington

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 Registration Dates

Study Start Date2023-08-01
Study Completion Date2025-05-31

Study Record Updates

Study Start Date2023-08-01
Study Completion Date2025-05-31

Terms related to this study

Keywords Provided by Researchers

  • endothelial function
  • brain blood flow
  • cognition

Additional Relevant MeSH Terms

  • Cardiovascular Diseases
  • Hypertension
  • Cognitive Decline
  • Diet
  • Healthy