Making Meals With Pulses

April 22, 2026 updated by: Shanon Casperson, USDA Grand Forks Human Nutrition Research Center

Understanding the Representation of Pulses and Pulse-based Food Products in the Diet of American Non-Vegetarian Consumers

The goal for this study is to determine how Americans use beans, peas, and lentils (also called pulses) as part of a meal. The researchers will investigate food choices when getting a meal or dish ready that is made of more than two foods. Secondly, they will determine how study participants feel about eating pulses.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The goal for this study is to determine how Americans view whole pulses and pulse-based food products as part of the meal/dish structure. The experimental approach researchers will use to address this goal is a meal/dish-composition computer task to investigate spontaneous food choices when other protein foods, vegetables, and grains are provided as meal/dish component options. For each meal or dish composition that pulses are chosen as a component, participants will be asked if the pulse/pulse-based food product was chosen as a substitute for another food.

Study Type

Observational

Enrollment (Estimated)

76

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • North Dakota
      • Grand Forks, North Dakota, United States, 58203
        • Recruiting
        • USDA Grand Forks Human Nutrition Research Center
        • Contact:

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.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Community sample

Description

Inclusion Criteria:

  • able to understand and sign the consent form
  • able to provide own transportation to research center
  • non-smoking or does not use other tobacco products, including e-cigarettes
  • not planning to or currently attempting to gain or lose weight
  • free of any major medical or psychiatric condition that would interfere with participation
  • physically able to do the computer tasks
  • cook meals a minimum of three times per week for own self and/or household

Exclusion Criteria:

  • more than a 2 kg change in body weight within the past 3 months
  • participation in a weight loss diet/exercise program
  • diagnosed eating disorder
  • allergies or severe dislike for the foods used to complete the task
  • had bariatric surgery
  • cannot read or understand English

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
What foods are chosen to create a meal
Time Frame: 30 minutes
Record which foods are chosen by participants when asked to create a meal under different scenarios.
30 minutes
What food is chosen first to create a meal
Time Frame: 30 minutes
Record what food is chosen first by participants when asked to create a meal under different scenarios.
30 minutes
Frequency of pulses chosen to create a meal
Time Frame: 30 minutes
The number of times participants choose pulses when creating a meal under different scenarios.
30 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Shanon Casperson, PhD, USDA Grand Forks 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 Major Dates

Study Start (Actual)

March 30, 2026

Primary Completion (Estimated)

December 1, 2027

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

February 27, 2026

First Submitted That Met QC Criteria

February 27, 2026

First Posted (Actual)

March 5, 2026

Study Record Updates

Last Update Posted (Actual)

April 28, 2026

Last Update Submitted That Met QC Criteria

April 22, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • GFHNRC344

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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