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NCT06771765Completed

Soup Meal Satiety Study

Satiety Promoting Effects of Chia and Hemp Seeds

Source: ClinicalTrials.gov · Last updated 22 Aug 2025

Brief summary (registry, in English)

This study will investigate food ingredients that may provide fullness to healthy adults after a meal. The ingredients will be incorporated into a lunch meal, and measures of hunger and fullness will be evaluated for several hours after the meal. Study subjects must be able to travel to the USDA Nutrition Center in Beltsville Maryland at scheduled times during the study for meals and study measures.

Status (registry)
Completed
Study type
Interventional
Enrollment
24 (actual)
First submitted
7 Jan 2025
Start date
18 Feb 2025
Primary completion date
2 May 2025
Lead sponsor
USDA Beltsville Human Nutrition Research Center
Diseases
Obesity
NCT number
NCT06771765

What you commit to

  • Study type: Interventional
  • Participants enrolled: 24
  • From 18 Feb 2025 to the primary completion date, 2 May 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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 (thus during the study period)
  • Use of certain medications or supplements (prescription or over-the-counter) that may interfere with the study objectives

Other illness

  • Known (self-reported) allergy or adverse reaction to study foods
  • Presence of diabetes, diverticulitis, colitis, celiac disease, Crohn's disease, irritable bowel syndrome, gastrointestinal disease, pancreatic disease
  • History of bariatric surgery or other weight control surgery
  • Other medical, psychiatric, or behavioral factors that in the judgment of the Principal Investigator may interfere with study participation or the ability to follow the intervention protocol

Age

  • Younger than 25 years

Other

  • 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 GI obstruction
  • 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)

Who the study is looking for

  • \-

Age in the registry: 25 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
U.S. Department of Agriculture, Beltsville Human Nutrition Research Center
Coordinator of this site? Confirm its status
BeltsvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.