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Correlation study of painless delivery on perinatal depression and progeny

Correlation study of painless delivery on perinatal depression and progeny

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069575
Enrollment
Unknown
Registered
2023-03-21
Start date
2023-03-21
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

Perinatal depression

Interventions

Pregnant women undergoing natural childbirth:N/A

Sponsors

Nanjing Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women of childbearing age (18 to 45 years) who intend to have a natural birth

Exclusion criteria

Exclusion criteria: A pregnant woman who intends to have a caesarean section has a definite diagnosis of a mental illness (e.g., schizophrenia, depression, anxiety, paranoia, mania, post-traumatic disorder and obsessive-compulsive disorder).

Design outcomes

Primary

MeasureTime frame
Edinburgh Postnatal Depression Scale, EPDS;Pittsburgh sleep quality index, PSQI;

Secondary

MeasureTime frame
General information of offspring (sex, length, birth weight, Apgar score, number of NICUs stay after birth, number of days, feeding method, whether there are other complications, etc.);

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