Artificial Intelligence and Gestacional Diabetes

NCT07345143 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2026-01-15

No results posted yet for this study

Summary

Artificial intelligence (AI) technology can assist medical teams in remote monitoring and continuing education of women with gestational diabetes (GDM), potentially improving adherence to interventions and impacting outcomes. An AI remote monitoring model called "monitoring model for women with GDM using pharmacological therapy," created by the ChamouDr technical team, will be analyzed focusing on disease education, glycemic control monitoring, and therapeutic interventions. Women diagnosed with GDM are invited to participate in the study and sign a free and informed consent form. The AI tool is installed on the pregnant woman's cell phone, who receives instructions to collect capillary blood glucose 6 times a day according to the protocol, at home, and report the results via WhatsApp to the study tool. Algorithm generated by the AI model based on self monitoring of blood glucose (SMBG) informs about diabetes control in the last week. The dashboard is accessible via a web browser, and signals: in green and red for patients with satisfactory and unsatisfactory control, respectively. Thus, the AI model optimizes the team's time in analyzing and treating patients appropriately in a simple, cost-effective, and accessible way.

Conditions

  • Gestational Diabetes
  • Macrosomia, Fetal

Interventions

OTHER

monitoring model for women with gestacional diabetes using pharmacological therapy

Artificial Intelligence modell through WhatsApp® to remote monitoring gestacional diabetes in insulin treatment, focusing on disease education, glycemic control monitoring, and therapeutic interventions.

Sponsors & Collaborators

  • JOSE FERNANDO VILELA-MARTIN

    lead OTHER

Principal Investigators

  • José F Vilela-Martin, MD, PhD · Hospital de Base

  • Vanessa V Goulart, MD, MSc · Hospital de Base, Sao Jose do Rio Preto, Sao Paulo, Brazil

  • Ligia C Junqueira, MD · Hospital de Base, Sao Jose do Rio Preto, Sao Paulo, Brazil

  • Amanda T Lotierzo, MD · Hospital de Base, Sao Jose do Rio Preto, Sao Paulo, Brazil

  • Carolina C Amorim, MD · Hospital de Base, Sao Jose do Rio Preto, Sao Paulo, Brazil

  • Maria Amalia BC Cançado, MD · Hospital de Base, Sao Jose do Rio Preto, Sao Paulo, Brazil

  • Leticia A Mantoani, student · Hospital de Base, Sao Jose do Rio Preto, Sao Paulo, Brazil

  • Rodrigo F Zancaner · Chamoudr company

  • Rafael Beolchi · Chamoudr company

  • Lucas F Queiroz · Chamoudr company

  • Luciana N Cosenso-Martin, MD, PhD · Hospital de Base, Sao Jose do Rio Preto, Sao Paulo, Brazil

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-01
Primary Completion
2026-12-20
Completion
2027-12-20

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07345143 on ClinicalTrials.gov