RECRUITING

Soup and Bread Recipe Impacts on Ingestive Behavior

Conditions

Obesity &Amp; Overweight chia seeds satiety weight management

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Voluntary Intake of Seed Enhanced Lunch Foods

Quick Facts

Study Start:2025-08-05

Study Completion:2025-11-05

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT07146958

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.

Ages Eligible for Study:25 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
Age 18 years or older Willing and able to provide informed consent Able to understand and follow study procedures Stable medical condition	* 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 Principal Investigator may interfere with study participation or the ability to follow the study plan

Inclusion Criteria

Exclusion Criteria

Age 18 years or older
Willing and able to provide informed consent
Able to understand and follow study procedures
Stable medical condition

* 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 Principal Investigator may interfere with study participation or the ability to follow the study plan

Contacts and Locations

Study Contact

Rita Rawal, PhD

CONTACT

240-328-4779

Rita.Rawal@usda.gov

Principal Investigator

Janet Novotny, PhD

PRINCIPAL_INVESTIGATOR

United States Department of Agriculture (USDA)

Study Locations (Sites)

U.S. Department of Agriculture, Beltsville Human Nutrition Research Center

Beltsville, Maryland, 20705

United States

Collaborators and Investigators

Sponsor: USDA Beltsville Human Nutrition Research Center

Janet Novotny, PhD, PRINCIPAL_INVESTIGATOR, United States Department of Agriculture (USDA)

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 Registration Dates

Study Start Date2025-08-05

Study Completion Date2025-11-05

Study Record Updates

Study Start Date2025-08-05

Study Completion Date2025-11-05

Terms related to this study

Keywords Provided by Researchers

chia seeds
satiety
weight management

Additional Relevant MeSH Terms

Obesity &Amp; Overweight