Phase
Condition
N/ATreatment
Ready-to-eat beef in frozen, 5-oz packages
Ready-to-eat beef in frozen, 1-oz packages
Clinical Study ID
Ages 19-24 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Provision of signed and dated informed consent form
Stated willingness to comply with all study procedures and lifestyle considerationsand availability for the duration of the study
Males and females; Age 19-24
Willingness to adhere to the ready-to-eat beef intervention regimen
Enrolled at University of Nebraska-Lincoln
BMI between 18.5 and 39.9
Not pregnant or nursing
No history of cognitive or metabolic diseases indicated by diagnosis, includingneurodegenerative disease, stroke, Type 1 and 2 diabetes, metabolic syndrome,cardiovascular disease, liver disease, kidney disease, and cancer
No history of eating or anxiety disorders
Willing to discontinue dietary supplement use throughout the duration of the study,if they are consuming supplement at the time of the registration
No known contraindication to MRI scans as determined by the MRI screening surveyquestions
Exclusion
Exclusion Criteria:
Current use of medications that may affect their responses to dietary intervention,such as amphetamines, antidepressants, anti-diabetic medications, laxatives,antibiotics, statins and diuretics.
Known intolerance or allergy to beef
Current use of nicotine products, including vaping
Previous use of nicotine products, including vaping, within the recent 6 months atthe time of pre-screening
Study Design
Study Description
Connect with a study center
University of Nebraska-Lincoln
Lincoln, Nebraska 68588
United StatesSite Not Available
University of Nebraska-Lincoln
Lincoln 5072006, Nebraska 5073708 68588
United StatesActive - Recruiting

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