Shenzhen Birth Cohort Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age15-49
SponsorSun Yat-sen University

About this trial

The Shenzhen Birth Cohort Study was set up to investigate the effect of early life environmental exposures on short- and long-term health consequences in Shenzhen, China.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

1. Pregnant women plan to delivery and participate in child care in our hospital; 2. Pregnant women plan to reside in Shenzhen for at least 7 years; 3. Pregnant women who show interest in the study and agree to provide informed consent; 4. Gestational weeks are less than 20 weeks.Those who will agree that their neonatal will be included in the study and be followed up regularly in our child health clinic until an age of 7 years.

Disqualifiers

Pregnant women who have been pregnant for more than 20 weeks; refuse to participate; unable to guarantee delivery in our hospital or can't participate in child care in our hospital; mentally incapacitated and need guardians; or be unwilling to sign informed consent.

Trial population

Pregnant women attending their first routine antenatal examinations and their partners and offspring.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • No intervention

    Other intervention

    This cohort study have any no intervention.

Treatment groups

10,000 Participants
are divided into 1 treatment group
Group A: No treatment1 intervention

Trial outcomes

Primary outcomes

1

Fetal outcomes.

Including intrauterine growth retardation, abortion, stillbirth, live birth, preterm. birth, low birth weight, macrosomia and birth defects.

Time frame
At delivery.

Secondary outcomes

1

Maternal weight changes (kg).

Assess using electronic weighing machine.

Time frame
At pre-pregnancy period, 20 weeks of gestation, 28 weeks of gestation, the time before labor and 30 days after delivery.
2

Number of participant with gestational complications.

Including gestational hypertension and preeclampsia, and gestational diabetes mellitus.

Time frame
At delivery.
3

Number of participant with postnatal depression.

Assess using Edinburgh Postnatal Depression Scale (EPDS).

Time frame
At 30 days after delivery, 3 months, 6 months after delivery.
4

Physical development.

Including weight changes (kg) and height changes (cm).

Time frame
at age of 1 month, 3 months, 6months, 1 year, 3 years and 6 years.

Other outcomes

Sponsors and contacts

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