Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
FEMALE
Healthy Volunteers
ID05503849

Born In Guangzhou Intervention Study Combining Dietary, Physical Activity, and Lifestyle Changes During Pregnancy to Improve Maternal and Infant Outcomes

Led by Guangzhou Women and Children's Medical Center · Updated on 2025-04-10

1160

Participants Needed

2

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a package of interventions combining diet, physical activity, and lifestyle changes during pregnancy to improve outcomes for mothers and their infants. This study focuses on pregnant women and aims to measure effects on pregnancy complications, child development, and maternal health over an extended period. The study is sponsored by Guangzhou Women and Children's Medical Center and involves behavioral intervention rather than drug treatment. Participants are randomly assigned to either a proactive management group receiving guidance on balanced diet, sufficient exercise, and lifestyle adjustments such as sleep and sun exposure, or to a group receiving standard prenatal care without extra intervention. The intervention is designed to begin before 20 weeks of pregnancy and continues through delivery and postpartum periods. During the study, mothers and children will undergo assessments including measurements of maternal weight change during pregnancy until one month postpartum, newborn size and skinfold thickness at birth, and long-term tracking of blood lipid, glucose, and insulin profiles up to six years after delivery. Child growth and neurological development are evaluated at multiple time points including six months, one year, three years, and six years of age. Maternal physical strength and body composition are also monitored around delivery. The study involves a double-blind design with long-term follow-up to monitor safety and effectiveness outcomes.

CONDITIONS

Brief Title

Born In Guangzhou Intervention Study

Who Can Participate

Age: 18Years - 50Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women attending prenatal care at Guangzhou Women and Children's Medical Center before 20 weeks' gestation
  • Pregnant women planning to deliver at Guangzhou Women and Children's Medical Center
  • Pregnant women intending to reside in Guangzhou for at least 3 years
  • Female participants aged 18 to 50 years
Not Eligible

You will not qualify if you...

  • Multiple pregnancies
  • Existing medical conditions such as uncontrolled diabetes, hypertension, thyroid disease, serious cardiovascular diseases, respiratory or systemic disorders
  • Use of drugs including aspirin, metformin, or low molecular weight heparin
  • Women with reading and/or writing difficulties
  • Women with serious mental disorders
  • Women with eating disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - Up to 20 weeks' gestation

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - From enrollment until delivery

Participants engage in lifestyle modifications during pregnancy, including balanced dietary intake, sufficient physical activity, and changes in lifestyle such as sleep and sun exposure.

Regular visits during pregnancy as part of proactive health management

Postpartum Follow-up

Duration - Up to 6 years postpartum

Participants are followed up after delivery to assess maternal and infant outcomes including maternal weight change, blood profiles, and child growth and development.

Follow-up visits at 1 month, 6 months, 1 year, 3 years, and 6 years postpartum

Trial Site Locations

Total: 2 locations

1

Fuying Campus, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China

Guangzhou, China

Actively Recruiting

2

Zhujiang new town campus, Guangzhou Women and Children's Medical Center, China

Guangzhou, China

Actively Recruiting

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Research Team

Q

Qiu Qiu, Dr.

S

Songying Shen, Msc.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Published Research Related To This Trial