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Clinical Trials in China / NCT07499622
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Digital Health Intervention for Early Identification and Prevention of Gestational Diabetes Mellitus

NCT07499622 · tracked via the Priya Life Science China tracker
Sponsor
Peking University
Phase
Not applicable
Started
2026-06
Last updated
2026-03-30

Condition(s) studied

Gestational Diabetes Mellitus (GDM)

Investigational drug(s) / intervention(s)

Digital Health Lifestyle Intervention

Digital Health Lifestyle Intervention: Participants receive a digital health lifestyle intervention in addition to routine antenatal care. The intervention is delivered through a digital platform and includes online health education, individualized lifestyle guidance, self-management tools, health information delivery, and interactive consultation. The intervention focuses on gestational weight management, diet, physical activity, sleep, and early prevention of gestational diabetes mellitus among pregnant women identified as high risk.

Study summary

This study aims to develop and evaluate an early risk identification and digital health intervention strategy for gestational diabetes mellitus (GDM) among pregnant women in China. Gestational diabetes mellitus is a common pregnancy complication associated with adverse maternal and neonatal outcomes, including excessive gestational weight gain, macrosomia, cesarean delivery, and increased long-term risk of metabolic disorders in both mothers and offspring.

The study includes two components. First, retrospective multi-source clinical data from maternal health records will be used to develop and validate a risk prediction model for early identification of pregnant women at high risk of GDM. Second, pregnant women identified as high risk in early pregnancy will be enrolled in a multicenter randomized controlled trial and assigned to either a digital health intervention group or a usual care group. The intervention includes online health education, individualized lifestyle guidance, behavioral self-management tools, and interactive consultation through a digital platform. The primary outcome is the incidence of GDM diagnosed during pregnancy. Secondary outcomes include gestational weight gain, cesarean delivery, macrosomia, and other maternal and neonatal outcomes.

This study is expected to provide evidence for improving early risk assessment, intelligent warning, and prevention strategies for GDM in the context of maternal health management in China.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Pregnant women in early pregnancy (within 13 weeks and 6 days of gestation) * Planned delivery at a participating study hospital * Age 18 years or older * Singleton pregnancy * Identified as high risk for gestational diabetes mellitus by the study risk assessment model * Willing and able to provide informed consent Exclusion Criteria: * • Pre-pregnancy diabetes mellitus or overt diabetes diagnosed at the first antenatal visit (fasting blood glucose greater than or equal to 7.0 mmol/L) * Pre-existing hypertension, autoimmune disease, major infection, or severe liver or kidney disease * Use of medications that affect glucose metabolism, such as corticosteroids or metformin * Severe psychiatric disorders * Inability or unwillingness to comply with study procedures

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Beijing Tongzhou Maternal and Child Health Hospital Beijing Beijing Municipality
Weifang Maternal and Child Health Hospital Weifang Shandong

More Peking University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07499622 on ClinicalTrials.gov ↗ ← All trials in China