Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorGuangzhou Women and Children's Medical Center
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 groupsSponsors and collaborators
Source ClinicalTrials.gov