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Health Effects of Grain Foods in Adults

Health Effects of Grain Foods in Adults

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06339879
Enrollment
120
Registered
2024-04-01
Start date
2024-01-18
Completion date
2026-12-31
Last updated
2024-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Whole Grain and Low Sugar, Low Whole Grain and High Sugar, Low Whole Grain and Low Sugar, Medium Whole Grain and Low Sugar

Keywords

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

Brief summary

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.

Detailed description

This 16-week, randomized, controlled, parallel-arm, clinical trial will assess the effects of consuming four different categories of grain foods on taste hedonics, appetite, food/energy intake, body weight, and blood pressure as well as acute and longer-term glycemia and lipemia. It will also examine the effects of foods varying in grain/carbohydrate composition on the microbiome and microbiota functionality. One hundred and twenty adults will be recruited and randomly assigned to one of four intervention groups. These groups will be defined by the diets they are prescribed. All will be prescribed diets containing approximately 50%; 35% and 15% energy from carbohydrate, fat and protein, respectively. Grain foods will comprise 50% of the carbohydrate component (i.e., 25% of total energy). The grain foods will be assigned to one of four categories based on whole grain content and concentrations of added sugars. The grain foods meeting these criteria will have the following composition: Group 1 - High Whole Grain, Low Sugar 6 servings of whole grain and \<13% energy from added sugars. Group 2 - Low Whole Grain, Low Sugar 3 servings of whole grain and \<13% energy from added sugars. Group 3 - High Whole Grain, High Sugar 6 servings of whole grain and \>13% energy from added sugars. Group 4 - Low Whole Grain, High Sugar 3 servings of whole grain and \>13% energy from added sugars. Detailed Study Design The study measures and timing are outlined in the following table: Screening Week 1 Baseline Week 2 Week 5 Week 8 Week 11 Week 14 Fasting Blood X X X XX MTT X X X Weight X X X X X X Body Composition X X CGM X X X Intake X Hedonics (palatability) X X X Appetite X X X Activity X X X Blood Pressure X X X X X X Microbiota X X X X X Compliance X X X X X MTT = Meal Tolerance Test; DXA= Dual-energy X-ray Absorptiometry; CGM=Continuous glucose monitoring

Interventions

OTHERHigh Whole Grain, Low Sugar

6 servings of whole grain and \<13% energy from added sugars.

OTHERLow Whole Grain, Low Sugar

3 servings of whole grain and \<13% energy from added sugars.

OTHERHigh Whole Grain, High Sugar

6 servings of whole grain and \>13% energy from added sugars.

OTHERLow Whole Grain, High Sugar

3 servings of whole grain and \>13% energy from added sugars.

Sponsors

Grain Foods Foundation
CollaboratorUNKNOWN
Purdue University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Parallel assignment

Eligibility

Sex/Gender
ALL
Age
21 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* male and female; 21 to 60 years old; Hemoglobin A1c concentration between 5.7 and 6.4% * 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. * low customary intake of whole grain foods (less than 2 servings per day) and high energy from added sugar (greater than 10% energy).

Exclusion criteria

* 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. * smoker * intended weight loss or gain during the study period; intended change of activity level during the study period * use of blood thinners * prior gastrointestinal surgery.

Design outcomes

Primary

MeasureTime frameDescription
Glycemia12 weeksblood sugar

Secondary

MeasureTime frameDescription
Taste Hedonics12 weekspalatability
Energy Intake12 weekskcals
Appetite12 weeksingestive sensations measured by VAS ratings scale 1 (lowest) - 100 (highest)
Systolic and Diastolic Blood Pressure12 weeksmm mercury
Lipemia12 weeksBlood lipids
Body Weight12 weekspounds

Countries

United States

Contacts

Primary ContactJudy George, BS
georgej@purdue.edu4654946192
Backup ContactRichard Mattes, PhD
mattes@purdue.edu7654940662

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026