ACTIVE_NOT_RECRUITING

WHNRC (Western Human Nutrition Research Center) Honey Study

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 purpose of this research is to compare two snacks, one with honey and nuts and the other with sugar and nuts, on glucose levels before and after eating these snacks. The investigators hypothesize that honey and nuts will have an additive effect on the reduction of postprandial glucose response. The investigators further hypothesize that consumption of honey paired with nuts will retain the benefit of sugar consumption in satiety and reduction of metabolic stress.

Official Title

WHNRC (Western Human Nutrition Research Center) Honey Study

Quick Facts

Study Start:2024-01-16
Study Completion:2026-10-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06107231

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 40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Women must be pre-menopausal
  2. * Willing to consume snacks that contain honey, table sugar, and tree nuts
  1. * Body Mass Index (BMI) \<18.5 or \>40
  2. * Allergies to tree nuts
  3. * Current medical diagnoses of chronic diseases including cardiovascular or pulmonary diseases, renal diseases, cancer, type 1 or type 2 diabetes, thyroid disease requiring medication, inflammatory or irritable bowel diseases, or those with recent major surgeries
  4. * No individuals who fall in to the vulnerable categories of adults including those unable to consent, pregnant women, children, or prisoners will be eligible for this study
  5. * Routinely taking medications known to affect glucose response.
  6. * Caffeine and alcohol use will not be excluded, but should be carefully reported by each subject.
  7. * Post-menopausal
  8. * Women who have been pregnant or nursing within the last 6 months or plan to become pregnant during the trial will be ineligible

Contacts and Locations

Principal Investigator

Mary Kable, PhD
PRINCIPAL_INVESTIGATOR
USDA, ARS, Western Human Nutrition Research Center
Nancy Keim, PhD
PRINCIPAL_INVESTIGATOR
USDA, ARS, Western Human Nutrition Research Center
Kevin Laugero, PhD
PRINCIPAL_INVESTIGATOR
USDA, ARS, Western Human Nutrition Research Center

Study Locations (Sites)

USDA, ARS, Western Human Nutrition Research Center
Davis, California, 95616
United States

Collaborators and Investigators

Sponsor: USDA, Western Human Nutrition Research Center

  • Mary Kable, PhD, PRINCIPAL_INVESTIGATOR, USDA, ARS, Western Human Nutrition Research Center
  • Nancy Keim, PhD, PRINCIPAL_INVESTIGATOR, USDA, ARS, Western Human Nutrition Research Center
  • Kevin Laugero, PhD, PRINCIPAL_INVESTIGATOR, USDA, ARS, Western Human Nutrition Research Center

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 Date2024-01-16
Study Completion Date2026-10-30

Study Record Updates

Study Start Date2024-01-16
Study Completion Date2026-10-30

Terms related to this study

Keywords Provided by Researchers

  • Satiety
  • Cognition
  • Cortisol
  • Glucose
  • Honey
  • Nuts
  • Saliva
  • Stool
  • Almonds
  • Sucrose

Additional Relevant MeSH Terms

  • Postprandial Glycemia
  • Metabolic Stress
  • Cognitive Change
  • Satisfaction, Personal