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Appetite Responses to Cereal Products

G

General Mills

Status

Completed

Conditions

Satisfaction, Consumer

Treatments

Other: Ready to Eat Cereal

Study type

Interventional

Funder types

Industry

Identifiers

NCT05855837
2023/03/21

Details and patient eligibility

About

The purpose of this clinical trial is to investigate appetite responses to 2 cereal products in healthy adults.

Enrollment

228 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

228 participants in 3 patient groups

Cereal Product 1
Experimental group
Description:
Ready to Eat Cereal Product 1 with 6 oz of skim milk
Treatment:
Other: Ready to Eat Cereal
Cereal Product 2
Experimental group
Description:
Ready to Eat Cereal Product 2 with 6 oz of skim milk
Treatment:
Other: Ready to Eat Cereal
Control
No Intervention group
Description:
No intervention (i.e., no food provided)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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