Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
PepsiCo Global R&D
Participant eligibility will be screened at visit 1. The study will be a single-arm intervention design. The study procedures will include a pre-study visit, a pre-intervention baseline data collection period, a 14 day intervention period, and an end of study visit.
Age
7–12
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Between the ages of 7-12 yrs.
Low fiber eater (\<14 g/d)
Accustomed to eating breakfast at home
Demonstrates spoken and written English literacy
Parent/or legal guardian has experience using a cell phone camera
Parent/or legal guardian is capable of emailing and texting photos by using cell phone features that enable this such as the select and attach option
Able to provide assent with parent and/or legal guardian after review of study protocol and procedures
Parent and/or legal guardian will also be required to provide consent on behalf of the child after reviewing study protocol and procedures
You may not be if
Use of enemas, laxatives, proton pump inhibitors, or antibiotics within the past 3 months
Use of fiber supplements such as fiber gummies (inulin/chicory root), or Metamucil or Citrucel
Use of vitamin/mineral supplements, multivitamins, or herbal supplements.
Participation in any other clinical trial up to 6 months before day 1 of participation in this study
History of medical or surgical events that may significantly affect the study outcomes including diagnosed gastric or digestive diseases
Not a regular breakfast eater at home
High-fiber eater (\>14 g of fiber per day)
Allergies to any of the ingredients in the test products
Children taking medication that affects appetite (i.e. certain ADHD medications that depress appetite)
Clareo Health | The Effect of Hot Cereal on Digestive Health in Children
