AI helper (Tia Bete) on WhatsApp to assist with carb counting and insulin dosing for people with type 1 diabetes
Official title: Efficacy and Safety of an Artificial Intelligence Tool for Carbohydrate Counting (Tiabete) in Children and Adults With Type 1 Diabetes Mellitus
Run by University of Sao Paulo · NCT07150052 · Data updated 2026-11-12
This trial will test whether an AI tool delivered via WhatsApp can help children and adults with type 1 diabetes count carbohydrates and adjust insulin doses more accurately.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 6 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | University of Sao Paulo Academic / other |
| Locations | 1 site (São Paulo, São Paulo) |
| Status | Recruiting |
| Started | May 1, 2025 |
| Main results expected | October 2025 |
| Study ends | December 2026 |
| Registry record updated | September 2, 2025 |
| Trial ID | NCT07150052 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are people with type 1 diabetes aged 6 years and older (with caregiver support for children), on a basal-bolus regimen, with HbA1c 7.2–10.5% in the past six months, who use WhatsApp and can follow study instructions.
✕Probably not a fit
Patients who cannot use WhatsApp, are illiterate, cannot attend periodic clinic visits, or interact with the tool less than three days per week are unlikely to benefit from this intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, longitudinal interventional study testing the AI-based tool Tia Bete, which gives real-time carbohydrate-counting and insulin-dose recommendations via WhatsApp using personalized insulin-to-carbohydrate ratios and insulin sensitivity factors. Participants include children (6–18 years) with caregiver involvement and adults over 18 who are on a basal-bolus insulin regimen and have recent HbA1c between 7.2% and 10.5%. The protocol requires regular outpatient follow-up at the University of São Paulo and a minimum frequency of interaction with the tool during the study. Key exclusions include inability to use WhatsApp, illiteracy, failure to follow instructions, or interacting with the tool fewer than three days per week.
Why it matters
Potential benefit: If successful, the tool could improve carb-counting accuracy and lead to better daytime blood sugar control with fewer dosing errors.
How similar studies have gone: App- and AI-based carb-counting tools have shown promising improvements in meal dosing accuracy in some adult studies, but pediatric data and WhatsApp-delivered AI support remain limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of type 1 diabetes mellitus * children between 6 and 18 years old and their caregivers; and adults \> 18 years old. Glycated Hb between 7.2-10.5% in the last 6 months. Being on a basal-bolus regimen Participating in and understanding the guidelines on how to use the program to be tested in this study Agreeing to the free and informed consent form. Performing periodic monitoring at the DM outpatient clinic at HC-FMUSP Exclusion Criteria: * Not understanding the instructions. * Being illiterate * Not attending the visits proposed by the study * Not using the tool via WhatsApp. * Not accepting consent. * Interacting with the tool less than 3 days a week during the study period.
Where it's running
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University of Sao Paulo
São Paulo, São Paulo, Brazil Recruiting
Study contacts
- Study coordinator: Caroline Gb Passone, Endocrinologist
- Email: carol.passone@gmail.com
- Phone: +5511981467909
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.