Fiber mHealth Intervention for Prediabetes
ConditionPrediabetes
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-39
SponsorUniversity of Oklahoma
About this trial
This is a single-arm feasibility trial to examine an mHealth intervention that combines high fiber education, home-delivered high fiber foods, and use of continuous glucose monitors.
Eligibility criteria
Qualifiers
Pre-diabetes based on HbA1c
Young adult, aged 18-39 years
Reside near Tulsa metro area
Ability to access/use a compatible smartphone
Disqualifiers
Suspected eating disorder
Current glucagon-like peptide-1 receptor agonist use
Food allergies or intolerances
Currently pregnant or breastfeeding
Trial design
Treatments tested in this trial
- GO-FAR
Treatment groups
80 Participants
are divided into 1 treatment groupLocations
1University of Oklahoma Health Campus74135, TulsaOklahoma, United States
Sponsors and collaborators
University of Oklahoma
Lead sponsor
Source ClinicalTrials.gov