- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07451119
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
- Name: Shanon Casperson, PhD
- Phone Number: 701-795-8497
- Email: shanon.casperson@usda.gov
Study Locations
-
-
North Dakota
-
Grand Forks, North Dakota, United States, 58203
- Recruiting
- USDA Grand Forks Human Nutrition Research Center
-
Contact:
- Angela J Scheett, MPH, RDN
- Phone Number: 701-795-8386
- Email: angela.scheett@usda.gov
-
-
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.