Status:
COMPLETED
Protein Quality on Appetite Control, Reward-driven Eating, & Subsequent Food Intake
Lead Sponsor:
University of Missouri-Columbia
Conditions:
Appetite and General Nutritional Disorders
Eligibility:
All Genders
18-30 years
Phase:
NA
Brief Summary
To determine whether the consumption of a beef-rich lunch improves appetite control, satiety, and energy intake regulation while reducing food reward and food cravings compared to the consumption of a...
Detailed Description
A randomized, crossover design, acute study was completed in 21 healthy adults (age 23 ±1 y; BMI: 23.8 ± 0.6 kg/m2) to compare 400 kcal lunch meals varying in protein quality. Two separate comparisons...
Eligibility Criteria
Inclusion
- Age range 18-30 y
- Normal to Overweight (BMI: 18-29.9 kg/m2)
- No metabolic, psychological, or neurological diseases/conditions
- Not currently/previously on a weight loss or other special diet (in the past 6 months)
- Not a vegetarian
- Right-handed (necessary for the fMRI analyses)
- Not pregnant
- Meets the MU-Brain Imaging Center Screening Criteria
- Have not given blood (for the American Red Cross in the past 6 months)
Exclusion
- Age \>30 y and \<18y
- Under Weight or Obese (BMI: \<18 kg/m2 or \>29.9 kg/m2)
- Clinically diagnosed with diabetes (Type I or Type II), having an eating disorder, or having any other metabolic, psychological, or neurological diseases/conditions that would influence the study outcomes.
- Currently/previously on a weight loss or other special diet (in the past 6 months)
- Left-handed
- Claustrophobic (≥ 2 past bouts of claustrophobia when exposure to small spaces)
- Do not meet the fMRI criteria established by the MU-BIC (regarding metal implants, etc.)
- Pregnant
- Does not meeting the MU-Brain Imaging Center screening criteria
- Have given blood (for the American Red Cross) in the past 6 months or plan to give blood in the following 6 months
Key Trial Info
Start Date :
May 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2014
Estimated Enrollment :
21 Patients enrolled
Trial Details
Trial ID
NCT02285907
Start Date
May 1 2012
End Date
March 1 2014
Last Update
May 15 2019
Active Locations (1)
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1
University of Missouri
Columbia, Missouri, United States, 65211