Peking University Birth Cohort in Weifang (PKUBC-WF)

P

Peking University

Status

Not yet enrolling

Conditions

Anemia
Gestational Diabetes
Child Development
Health Problems in Pregnancy
Gestational Hypertension
Mother-Infant Interaction
Obesity
Pregnancy Outcomes
Preterm Birth

Treatments

Other: No Interventions

Study type

Observational

Funder types

Other

Identifiers

NCT06234332
PKUBC-WF

Details and patient eligibility

About

The PKUBC-WF is a prospective cohort study carried out in Weifang city of Shandong, China. The primary aim of this study is to investigate the short-term and long-term effects of pre-pregnant and prenatal exposure on maternal and child health. Data are collected regarding environmental, nutritional and lifestyle exposures as well as short-term and long-term health outcomes of mothers and their children from birth to before 18 years old. Biological samples including peripheral blood, urine, placenta, umbilical cord, cord blood, and faeces are also collected.

Full description

Maternal and child health is of great concern globally. Early life phase of a fetus and infant is a critical period for the development of health and disease in the whole life. Exposure of negative environmental, nutritional and lifestyle factors in pregnant women during this period can have adverse effects on fetal and infant. In addition, for mothers, complications during pregnancy could also have a negative effect on long-term health of mothers, such as diabetes, hypertension. Thus, the Peking University Birth Cohort in Weifang is primarily aimed to investigate the short-term and long-term effects of pre-pregnant and prenatal exposure on maternal and child health. Data are collected regarding environmental, nutritional and lifestyle exposures as well as short-term and long-term health outcomes of mothers, husbands and their children from birth to before 18 years old. Biological samples including peripheral blood, urine, placenta, umbilical cord, cord blood, and faeces samples are also collected.

Enrollment

2,800 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Pregnant woman

    1. Pregnant women, 6-13^+6 gestational weeks
    2. Resided in Weifang in the past half years and have no plan to move out after delivery
    3. Pregnant women who plan to have antenatal care and delivery in Weifang maternal&Child Hospital.
    4. Pregnant women who is willing to participate in this study with informed consent
  • Pregnant woman's husband

    1. His wife was eligible for enrollment
    2. He is the biological father of the child (his wife's current pregnancy)
    3. Pregnant women's husband who is willing to participate in this study with informed consent
  • Offspring 4. Children born to pregnant women who met the inclusion criteria after enrolling in this study.

    1. Before the age of 8 years, his/her mother provided written informed consent. 6. After 8 years old, he/she agreed to continue this study and signed the informed consent.

Exclusion criteria

  • Participants who cannot communicate normally.

Trial design

2,800 participants in 2 patient groups

Exposure group
Description:
Group with environmental, nutritional or lifestyle exposures
Treatment:
Other: No Interventions
Non-exposed group
Description:
Group without any environmental, nutritional and lifestyle exposures

Trial contacts and locations

1

Loading...

Central trial contact

Haijun Wang, Ph.D; Jue Liu, Ph.D

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems