Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
31 participants
OBSERVATIONAL
2012-07-31
2014-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Impact of a Satiating Diet in Obese Men With a Low Satiety Phenotype
NCT03128697
The Effect of Time-restricted Feeding on Physiological Function in Middle-aged and Older Adults
NCT02970188
The Relationship Between Blood Glucose and Satiety Ratings
NCT04183855
Effect of Food Form on Satiety and Gastric Emptying
NCT01102907
Hunger, Satiety, and Metabolic Responses to High-fat Meals of Varying Fatty Acid Composition
NCT02966444
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* non-smoking
* not taking steroid-based medications
* not planning to or currently attempting to gain or lose weight
* being willing to consent to study conditions
* healthy adults ages 25-45 years
* body mass index between 18-30 kg/m2.
* University of North Dakota students may participate but student status is not required.
Exclusion Criteria
* current or planned pregnancy
* lactation
* unmanaged hypertension (systolic \>160 mmHg or diastolic \> 100mmHg) and/or other cardiovascular, pulmonary, skeletal and metabolic diseases
* taking medications known to affect appetite, body composition, weight, or food intake
25 Years
45 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
USDA Grand Forks Human Nutrition Research Center
FED
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Susan K Raatz, PhD
Role: PRINCIPAL_INVESTIGATOR
USDA GFHNRC
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
USDA Human Nutrition Research Center
Grand Forks, North Dakota, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
GFHNRC504
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.