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Prevention of induced abortion among postpartum women: a prevalence survey and intervention study in China

Prevention of induced abortion among postpartum women: a prevalence survey and intervention study in China

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023790
Enrollment
Unknown
Registered
2019-06-12
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

Postpartum contraceptive use and induced abortion

Interventions

Postpartum women:Questionnaire investigation, no intervention
Experimental group (randomly allocation):IEC, counseling, providing contraceptives
Control group (randomly allocation):Routine management

Sponsors

Shanghai Institute of Planned Parenthood Research
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 49 Years

Inclusion criteria

Inclusion criteria: 1. Pregnant women who voluntarily receive prenatal examination and delivery at the participating hospitals with gestational age 36 or more weeks; 2. Must sign the informed consent form and be willing to accept the prenatal and postnatal investigation and follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients with any serious health problems and/or mental disorders that may affect subjects' investigation and follow-up; 2. Have dysgraphia or language expression disorder.

Design outcomes

Primary

MeasureTime frame
indicence of induced abortion at 12 months after delivery;

Secondary

MeasureTime frame
prevalence of contraceptive use 12 months after delivery;incidence of unintended pregnancy 12 months after delivery;

Countries

China

Contacts

Public ContactDr Yan Che

Shanghai Institute of Planned Parenthood Research

cheyan2004@163.com+86 021 64042328

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 9, 2026