Appetite Responses to Cereal Products
- Conditions
- Satisfaction, Consumer
- Interventions
- Other: Ready to Eat Cereal
- Registration Number
- NCT05855837
- Lead Sponsor
- General Mills
- Brief Summary
The purpose of this clinical trial is to investigate appetite responses to 2 cereal products in healthy adults.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 228
- Healthy adults 18-70 years old
- Habitual cereal consumers (at least several times per month)
- Body mass index 18.5-24.9 kg/m2 (based on self-reported weight and height
- Understand and willing to follow the study procedures
- Willing to drink skim milk
- Willing to maintain habitual diet, physical activity pattern, and body weight throughout the study
- Willing to abstain from strenuous exercise and consuming alcoholic drinks 24 hours before the test day
- Willing to provide Informed Consent to participate in the study
- Pregnant or lactating women, or women who are planning to become pregnant during the study
- Known food allergies, sensitivities, or intolerance to any food or food ingredients
- Participation in another clinical trial for food, investigational drug, nutritional supplement, or lifestyle modification
- Taking medication(s) that affect appetite, metabolism or blood pressure
- Presence of acute diseases or infection
- Presence or history of chronic diseases
- Diagnosed with an eating disorder
- Restraint eaters as determined by score >4 from the Dutch Eating Behavior Questionnaire
- Lost or gained 5 or more pounds in the past 3 months
- On a weight loss diet or undergoing intermittent fasting
- COVID-19 infection within the past 3 months
- Subjects who do not eat cereal products
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Cereal Product 1 Ready to Eat Cereal Ready to Eat Cereal Product 1 with 6 oz of skim milk Cereal Product 2 Ready to Eat Cereal Ready to Eat Cereal Product 2 with 6 oz of skim milk
- Primary Outcome Measures
Name Time Method Visual Analogue Scale for Desire to Eat 0-240 minutes 240 min Visual Analogue Scale for "how strong is your desire to eat right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more desire to eat. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.
Visual Analogue Scale for Fullness 0-240 minutes 240 min Visual Analogue Scale for "how full are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more fullness. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.
Visual Analogue Scale for Hunger 0-240 minutes 240 minutes Visual Analogue Scale for "how hungry are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more hunger. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.
Visual Analogue Scale for Satisfaction 0-240 minutes 240 min Visual Analogue Scale for "how satisfied are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more satisfaction. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.
Visual Analogue Scale for Satiation 0-240 minutes 0-240 min Visual Analogue Scale for "how satiated are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more satiation. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.
Visual Analogue Scale for Prospective Consumption 0-240 minutes 240 min Visual Analogue Scale for "how much do you think you can eat right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more prospective consumption. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Remote study, no physical facility
🇺🇸Minneapolis, Minnesota, United States