RecruitingNot ApplicableNCT07204470
The Effects of Four Instant Maize Porridges on Satiety Measures
Sponsor
PepsiCo Global R&D
Enrollment
50 participants
Start Date
Jul 21, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
This study is designed to test the hypothesis that whole-grain forms of maize meal enhance and prolong satiety post-meal consumption.
Eligibility
Min Age: 18 YearsMax Age: 35 Years
Inclusion Criteria7
- Availability to participate on the test days
- Interest and consent to participate in the study
- Participants must be willing to fast 10 hours overnight before the test breakfast meal (only water allowed)
- Products and meals high in fiber, alcohol and strenuous exercise should be avoided 24 hours before the test
- Age 18-35 years
- Healthy BMI: 18.5-24.9 kg/m2
- Equal split, males and females
Exclusion Criteria13
- Pregnancy; breast-feeding
- History of gastrointestinal disease having an impact on food absorption or digestion; anorexia nervosa or bulimia nervosa
- Anaemia
- Hypoglycaemia
- Cardiovascular disease; elevated plasma glucose; unstable thyroid function
- Abnormal/irregular menstrual cycle
- Substance abuse
- Being on medication which influences appetite
- Depression; smoking
- Participation in any weight altering program; weight gain or loss \> 5 kg in 3 months prior to enrolment
- History of intestinal discomfort when consuming relatively small (e.g., \<10g) amounts of non-digestible fibres
- Any known food allergies or intolerances such as wheat or soy; special diets prescribed by medical practitioner
- Any intensive physical training program
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Interventions
OTHERBreakfast cereal standardised to an isocaloric intake of approximately 350 kcal, consume entire portion within 15 minutes witnessed. No other food may be consumed during the 4 hour test period.
Cereal is in porridge form. One 350 ml bottle of water provided for the 4 hour test period 7:00-11:00 a.m.. Control dinner meal consumed the prior evening, then fast 10 hours overnight before visiting the test facility on four test days one week apart.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07204470
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