A Study to Evaluate the Effects of a Prebiotic Soda on Glycemic Control in Adults
ConditionBlood Glucose Control
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-70
SponsorOlipop, PBC
About this trial
The main objective of this study is to evaluate the chronic effects of replacing traditional non-diet soda with a prebiotic soda on biomarkers associated with glycemic control in adults with glucose dysregulation who are habitual consumers of traditional soda.
Eligibility criteria
Qualifiers
Able to provide informed consent
Willing to comply with all study procedures
Male or female, ages 30 - 70 years old
Habitual consumers of traditional non-diet soda (average intake 2 - 3 servings (24-36 fl. oz)/daily in a typical month, representing usual dietary pattern)
Disqualifiers
Inability to consume a standard 12 fl. oz. carbonated beverage twice daily
Currently engaged or planning to be on an intensive weight loss regimen program
Extreme dietary habits in the judgement of the Investigator or has been diagnosed with an eating disorder
Habitual use of fiber supplements, inulin-based supplements, acacia fiber, glucomannan, prebiotic supplements, or probiotic supplements within 30 days of study enrollment
Trial design
Treatments tested in this trial
- Prebiotic Soda
- Active Control
Treatment groups
224 Participants
are divided into 2 treatment groupsSponsors and collaborators
Olipop, PBC
Lead sponsor
People Science
Collaborator
Source ClinicalTrials.gov