Soup and Bread Recipe Impacts on Ingestive Behavior (NCT07146958) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Soup and Bread Recipe Impacts on Ingestive Behavior
United States24 participantsStarted 2025-08-05
Plain-language summary
The goal of the study is to determine the likability of seeds incorporated into lunch foods. The study will provide a better understanding of ways to make recipe alterations that may promote health and fullness.
Who can participate
Age range
25 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
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Exclusion Criteria:
* Younger than 25 years
* Known (self-reported) allergy or adverse reaction to study foods
* Women who have given birth during the previous 12 months or who are pregnant/lactating or who plan to become pregnant over the upcoming 6 months (which will overlap with the study period)
* Presence of diabetes, diverticulitis (inflammation of the large intestine), colitis (inflammation of the colon), celiac disease, Crohn's disease, irritable bowel syndrome, gastrointestinal disease, pancreatic disease
* History of bariatric surgery or other weight control surgery
* Removal of a portion of the stomach or gastrointestinal tract
* Actively trying to gain or lose weight at the time of the study recruitment or planning to gain or lose weight during the study periods
* Diminished sense of taste and/or smell
* Anorexia Nervosa and/or Bulimia
* Smoking, vaping, or use of tobacco products in the past 3 months
* Suspected or known physiological/mechanical gastrointestinal (GI) obstruction
* Use of certain medications or supplements (prescription or over-the-counter) that may interfere with the study objectives
* Unable or unwilling to give informed consent or communicate with study staff
* Self-report of alcohol or substance abuse within the past 12 months and/or current treatment for these problems (long-term participation in Alcoholics Anonymous is not an exclusion)
* Other medical, psychiatric, or behavioral factors that in the judgment of the …
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Lunch food intake
Timeframe: 30 minutes after the start of the intervention
2
Feelings of hunger
Timeframe: 30 minutes post treatment
3
Feelings of satisfaction
Timeframe: 30 minutes post intervention
4
Feelings of fullness
Timeframe: 30 minutes post intervention
5
Ability to consume more food
Timeframe: 30 minutes post intervention
6
Desire to eat something sweet
Timeframe: 30 minutes post intervention
7
Desire to eat something salty
Timeframe: 30 minutes post intervention
8
Desire to eat something savory
Trial details
NCT IDNCT07146958
SponsorUSDA Beltsville Human Nutrition Research Center