RECRUITING

Health Effects of Grain Foods in Adults

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

This study will assess the effects of eating whole grain foods versus refined grain foods with different amounts of added sugar. It is hypothesized that a diet including grain products will have beneficial effects on taste hedonics, appetite, food/energy intake, body weight, blood pressure, acute and chronic glycemia and acute and chronic lipemia compared to customary diets controlling for added sugars, saturated fats and sodium.

Official Title

Health Effects of Grain Foods in Adults

Quick Facts

Study Start:2024-01-18
Study Completion:2026-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06339879

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:21 Years to 60 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * male and female; 21 to 60 years old; Hemoglobin A1c concentration between 5.7 and 6.4%
  2. * Prefer no use of medications, but if on medication, must have been on a stable dose for 3 months and plan to remain at the same dose for the duration of the trial.
  3. * low customary intake of whole grain foods (less than 2 servings per day) and high energy from added sugar (greater than 10% energy).
  1. * Grain or dairy sensitivities or allergies or celiac disease; sensitivity or allergy to other foods that would result in refusal to eat a class of foods.
  2. * smoker
  3. * intended weight loss or gain during the study period; intended change of activity level during the study period
  4. * use of blood thinners
  5. * prior gastrointestinal surgery.

Contacts and Locations

Study Contact

Judy George, BS
CONTACT
4654946192
georgej@purdue.edu
Richard Mattes, PhD
CONTACT
7654940662
mattes@purdue.edu

Principal Investigator

Richard Mattes, PhD
PRINCIPAL_INVESTIGATOR
Purdue University

Study Locations (Sites)

Purdue University
West Lafayette, Indiana, 17907
United States

Collaborators and Investigators

Sponsor: Purdue University

  • Richard Mattes, PhD, PRINCIPAL_INVESTIGATOR, Purdue University

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 Date2024-01-18
Study Completion Date2026-12-31

Study Record Updates

Study Start Date2024-01-18
Study Completion Date2026-12-31

Terms related to this study

Keywords Provided by Researchers

  • whole grain
  • refined grain
  • glycemia
  • appetite
  • food intake
  • microbiome
  • body weight
  • blood pressure
  • lipemia
  • hedonics

Additional Relevant MeSH Terms

  • High Whole Grain and Low Sugar
  • Medium Whole Grain and Low Sugar
  • Low Whole Grain and Low Sugar
  • Low Whole Grain and High Sugar