Skip to main content
OpenTrials
Completed

NCT Number: NCT02391610

The China-Anhui Birth Cohort Study (C-ABCS)

The China-Anhui Birth Cohort Study (C-ABCS) was set up to examine the delayed, cumulative and interactive effects of maternal environmental exposures on birth outcomes and children's development. The C-ABCS recruited pregnant women from six major cities of Anhui province, China, between November 2008 and October 2010. A range of data (including demographic, obstetric, occupational, nutritional and psychosocial factors) were collected by both interviews and laboratory tests. In each trimester, women's blood samples were drawn, and pregnancy complications were abstracted from physician's medical records. By the end of 2011, birth outcomes/birth defects were observed/identified by clinicians within 12 months after the delivery of 11 421 singleton live births of six cities and those outcomes among the remaining 2033 live births are still being observed. In addition, 4668 children from Ma'anshan city will be further followed up during the pre-school period till they reach adolescence to obtain the data on familial environmental exposures as well as children's physical, psychological, behavioural and sexual development. The interview data and information on laboratory examinations are available on request from archives in the Anhui Provincial Key Laboratory of Population Health & Aristogenics.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Having been lived in local city at least 6 months;
  • Establishing maternal card in the hospital for the first time;
  • Gestational week ≤ 16 weeks;
  • Willing to have antenatal checkups and childbirth in the hospital where they establish maternal cards.

Exclusion criteria

  • Women who have abnormities in speaking and can not complete the survey by themselves;
  • Women with mental disorders;
  • Women who plan to leave local places.

Treatment and study plan

No intervention

Other

Primary outcomes

  1. Pregnancy outcomes and birth defects

    Time frame: Up to 12 months of age

    By clinical diagnosis, including abortion/premature birth/prolonged pregnancy/fetal death/stillbirth/live birth, Low birthweight/macrosomia/small for gestation age/large for gestation age, Structural birth defects and functional birth defects

Secondary outcomes

  1. Children's physical development

    Time frame: At ages of 1.5-3 and 4.5-6 years

    Including body height/length, body weight, blood pressure, blood lipoid

  2. Psychological and behavioural development

    Time frame: At ages of 1.5-3 and 4.5-6 years

    cognition, behaviour and temperament

  3. Family environmental exposure

    Time frame: At ages of 1.5-3 and 4.5-6 years

    Eating patterns and parenting style.

  4. Mental health problems

    Time frame: At ages of 1.5-3 & 4.5-6 years

    Mental retardation, attention deficit hyperactivity, disorder, autism spectrum disorders.

  5. Sexual development indicators

    Time frame: At ages of 9-15 years for boys, and 8-14 years for girls

    Secondary sexual characters, Sexual hormones.

Sponsors and collaborators

Lead sponsor

Fangbiao Tao

Other

Registry information

Official study title

A Prospective Population-based Cohort Study That Recruited 16766 Pregnant Women From Six Major Cities of Anhui Province in China

Important dates

Study start
2008
Primary completion
2010
Study completion
2015
First posted
Mar 18, 2015
Registry last updated
Mar 18, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.