University of Sao Paulo
São Paulo, 04026-001, Brazil
Location status: Recruiting
Location contact
CAROLINE PASSONE
CONTACT
CAROLINE PASSONE
PRINCIPAL_INVESTIGATOR
CONTACT
NCT Number: NCT07150052
IntroductionType 1 Diabetes Mellitus (T1DM) requires lifelong exogenous insulin therapy, along with self-management strategies, such as carbohydrate counting, to appropriately adjust insulin doses in response to meals. However, many patients face challenges in adhering consistently to carbohydrate counting, compromising glycemic control and increasing the risk of diabetes-related complications. Emerging technologies, such as artificial intelligence (AI), hold significant potential for optimizing disease management by enhancing the accuracy and efficiency of self-care practices. ObjectiveThe primary aim of this study is to evaluate the efficacy and safety of the AI-based tool Tia Bete, designed to assist patients with T1DM in carbohydrate counting and insulin dose adjustment. The tool provides real-time recommendations based on personalized insulin-to-carbohydrate ratios, insulin sensitivity factors, and individualized glycemic goals. MethodsThis is a prospective, longitudinal study involving 40 patients with T1DM, stratified into two cohorts: 20 children and adolescents (6-18 years) and 20 adults (>18 years), recruited at the Hospital das Clínicas, University of São Paulo (HCFMUSP). Participants will be assessed before and after six months of using the Tia Bete tool. Glycemic control will be evaluated using parameters such as glycated hemoglobin (HbA1c), time in range, and the incidence of hypoglycemia and hyperglycemia. Quality of life and satisfaction with the tool will also be assessed. Overview of the AI Tool Launched in June 2024, Tia Bete is an AI-based digital solution designed to facilitate glycemic control and improve quality of life for patients with T1DM. By offering real-time assistance with carbohydrate counting and insulin dose recommendations, the tool aims to enhance patient autonomy while enabling flexible treatment adherence in collaboration with their multidisciplinary healthcare team. Results and ConclusionsPreliminary data indicate high engagement, with over 35,000 active users interacting with the platform at least four times per week. Initial findings suggest significant improvements in glycemic control, as well as increased confidence in carbohydrate counting and insulin dose adjustments. The dissemination of this project is crucial for advancing T1DM care, offering a scalable, accessible, and effective technological solution. Final results are expected by October 2025.
Interested in participating?
Request Info6 year and older
All sexes
Interventional
Not applicable
São Paulo, 04026-001, Brazil
Location status: Recruiting
CAROLINE PASSONE
CONTACT
CAROLINE PASSONE
PRINCIPAL_INVESTIGATOR
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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
AI-based tool Tia Bete, designed to assist patients with T1DM in carbohydrate counting and insulin dose adjustment. The tool provides real-time recommendations based on personalized insulin-to-carbohydrate ratios, insulin sensitivity factors, and individualized glycemic goals.
Time frame: 6 months
Participants will be assessed before and after six months of using the Tia Bete tool. Glycemic control will be evaluated using :
Time frame: 6 months
Participants will be assessed before and after six months of using the Tia Bete tool. Glycemic control will be evaluated using :
Time frame: 6 months
Diabetes-specific health-related quality of life will be assessed with validated, age-appropriate instruments: the Pediatric Quality of Life Inventory (PedsQL) 3.0 Diabetes Module for children/adolescents (<18 years) and the Brazilian abridged version of the Diabetes Quality of Life Measure (DQOL-Brazil-8) for adults (≥18 years). Scores for both instruments range from 0 (lowest possible quality of life) to 100 (highest); higher scores indicate better quality of life.
Time frame: 6 months
Participant satisfaction with the intervention will be assessed using the Satisfaction Form with the Tia Bete Tool. The instrument yields a total score from 4 (minimum possible satisfaction) to 30 (maximum possible satisfaction); higher scores indicate greater satisfaction with the tool.
Contact information is provided by the study sponsor or research team.
University of Sao Paulo
Other
Acronym: Tiabete
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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