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Recruiting

NCT Number: NCT07525050

The Breakfast Study: How Different Aspects of Food Affect Eating

The purpose of this research study is to test how different aspects of food including food processing affect eating behaviors.

Recruiting

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Key information

Conditions

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

USDA ARS Grand Forks Human Nutrition Research Center

Grand Forks, North Dakota, 58203, United States

Location status: Recruiting

Location contact

Angela J Scheett, MPH, RDN

CONTACT

[email protected]

701-795-8386

About this study

The purpose of this project is to begin to address the current gap in research on ultra-processed foods (UPFs) and satiety with an acute feeding study that compares nutrient-dense meals containing mostly UPFs or "minimally processed" foods (MPFs) (mostly meaning ≥80% kcal) with similar food types and texture and macronutrient content to assess potential impacts on satiety, eating rate, food palatability, acceptance, and oral processing behaviors.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • do not have restrictive eating practices
  • regularly consume breakfast
  • able to understand and sign the consent form
  • have own transportation to the research center
  • not allergic to study foods or unwilling to eat them
  • willing to comply with study demands
  • able to read and understand English
  • available to attend two in-person visits on a weekday and/or Saturday morning from 7:15 a.m. to 12:15 p.m.

Exclusion criteria

  • taking statins, medication to lower blood pressure, anti-inflammatory, anti-diabetes, or weight-loss medications
  • pregnant, lactating, or planning to become pregnant
  • diagnosed with an eating disorder, hypothyroidism, or cancer
  • allergy to study foods or express unwillingness to consume them
  • have gained or lost more than 10 pounds in the last 3 months
  • regular participants in vigorous endurance or resistance exercise (e.g., marathons, endurance bike races, triathlons, CrossFit, powerlifting)

Treatment and study plan

UPF breakfast/MPF breakfast

Other

Participants will be provided with the UPF breakfast during the first study visit and the MPF breakfast during the second study visit

MPF breakfast/UPF breakfast

Other

Participants will be provided with the MPF breakfast during the first study visit and the UPF breakfast during the second study visit

Primary outcomes

  1. Difference in satiety as determined by visual analogue scales (VAS)

    Time frame: Day 1, Day 15

    Participants will complete visual analogue scales (VAS) on satiety measures during each study visit. VAS are represented by 100mm lines anchored at each end by descriptive extremes. For satiety, these extremes are statements about desire to eat (very weak; very strong), hunger (not hungry; as hungry as I've ever felt), fullness (not full; totally full), satisfied (completely empty; cannot eat another bite), prospective consumption (not at all; a large amount). Participants indicate via marks on the VAS line the extent to which they experience each sensation at a given timepoint. Measurements are tracked across time and plotted on a graph from baseline to the time preceding the next meal and the area under the curve above the baseline measurement is calculated.

Study contacts

Contact information is provided by the study sponsor or research team.

Julie Hess, PhD

CONTACT

[email protected]

701-795-8146

Sponsors and collaborators

Lead sponsor

USDA Grand Forks Human Nutrition Research Center

Fed

Collaborators

  • University of North Dakota

Registry information

Official study title

Impact of a Healthy Meal Containing Mostly Ultra-processed Foods Compared to a Healthy Meal With Less-processed Foods on Satiety and Eating Behaviors

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Apr 13, 2026
Registry last updated
Jun 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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