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Effects of prenatal anxiety on maternal and infant outcomes

Effects of prenatal anxiety on maternal and infant outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069464
Enrollment
Unknown
Registered
2023-03-17
Start date
2023-03-17
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Prenatal anxiety

Interventions

Group prenatal anxiety:No

Sponsors

Nanjing Maternal and child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Childbearing age (18 to 45 years); 2. Gestational age >= 37 weeks; 3. No history of organic disease, endocrine system disease, no history of mental illness; 4. Able to complete the questionnaire independently; 5. Pregnant women who volunteered to participate in this study planned caesarean section.

Exclusion criteria

Exclusion criteria: 1. Patients with consciousness disorder and communication difficulty; 2. People with a history of mental illness, personality disorder or intellectual disability; 3. Use antianxiety drugs and nerve blockers during pregnancy.

Design outcomes

Primary

MeasureTime frame
STAI score;

Secondary

MeasureTime frame
General information of pregnant women, intraoperative blood loss, postoperative VAS score, postoperative hospitalization days, general information of offspring (gender, length, birth weight, Apgar score, number of NICUs stay after birth, number of days, feeding method);

Countries

China

Contacts

Public ContactMing Jiang

Nanjing Maternal and child Health Care Hospital

njfyjiangming@163.com+86 13912961506

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026