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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02391610
Enrollment
16766
Registered
2015-03-18
Start date
2008-11-30
Completion date
2015-01-31
Last updated
2015-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Birth Defects, Children Development, Environmental Exposures, Other Pregnancy With Abortive Outcome

Keywords

birth cohort study, environmental exposures, birth defects, pregnant outcomes, children development

Brief summary

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.

Interventions

OTHERNo intervention

Sponsors

Fangbiao Tao
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
17 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

1. Having been lived in local city at least 6 months; 2. Establishing maternal card in the hospital for the first time; 3. Gestational week ≤ 16 weeks; 4. Willing to have antenatal checkups and childbirth in the hospital where they establish maternal cards.

Exclusion criteria

1. Women who have abnormities in speaking and can not complete the survey by themselves; 2. Women with mental disorders; 3. Women who plan to leave local places.

Design outcomes

Primary

MeasureTime frameDescription
Pregnancy outcomes and birth defectsUp to 12 months of ageBy 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

MeasureTime frameDescription
Children's physical developmentAt ages of 1.5-3 and 4.5-6 yearsIncluding body height/length, body weight, blood pressure, blood lipoid
Psychological and behavioural developmentAt ages of 1.5-3 and 4.5-6 yearscognition, behaviour and temperament
Family environmental exposureAt ages of 1.5-3 and 4.5-6 yearsEating patterns and parenting style.
Mental health problemsAt ages of 1.5-3 & 4.5-6 yearsMental retardation, attention deficit hyperactivity, disorder, autism spectrum disorders.
Sexual development indicatorsAt ages of 9-15 years for boys, and 8-14 years for girlsSecondary sexual characters, Sexual hormones.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026