Health Trials

About this trial

The main objective of this study is to test the efficacy of an intervention package (dietary, physical and lifestyle modification) during pregnancy in improving the clinical outcomes of mother-infant dyads.

Eligibility criteria

Qualifiers

Pregnant women attending prenatal care at Guangzhou Women and Children's Medical Center (GWCMC) <20 weeks' gestation

Pregnant women plan to deliver at GWCMC

Pregnant women intend to reside in Guangzhou for at least 3 years

Disqualifiers

Multiple pregnancies

Existing medical conditions (uncontrolled diabetes, hypertension or thyroid disease; other serious cardiovascular diseases, respiratory or systematic disorders)

Use of drugs (aspirin, metformin, low molecular weight heparin)

Women with reading and/or writing difficulties

Trial design

Treatments tested in this trial

  • Lifestyle modification

Treatment groups

1,160 Participants
are divided into 2 treatment groups

Locations

2
Fuying Campus, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China Guangzhou China
Zhujiang new town campus, Guangzhou Women and Children&#39;s Medical Center, China Guangzhou China

Sponsors and collaborators

Guangzhou Women and Children's Medical Center

Lead sponsor

Source ClinicalTrials.gov