Prenatal Education
Conditions
Interventions
This is a two-arm, randomized controlled clinical trial. The control group consisted of 66 pregnant women who answered a questionnaire, and the intervention group consisted of 67 pregnant women who an
however, during the study, three more participants were included, totaling 133. The sample size calculation was based on an estimated percentage of women with elective cesarean delivery in the interve
Sponsors
Faculdade de Medicina de Jundiaí
Faculdade de Medicina de Jundiaí
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Healthy pregnant women; in good overall health; who have opted for a cesarean section
Exclusion criteria
Exclusion criteria: Pregnant women with medical or obstetric indication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The expected result is that a healthy pregnant woman, after receiving clear information, will modify her opinion about choosing cesarean section as an option for delivery. | — |
Secondary
| Measure | Time frame |
|---|---|
| The expectation is that, with a better understanding of the factors influencing this choice, health policies and clinical practices can be adjusted to support more informed and safer childbirth choices. | — |
Countries
Brazil
Contacts
Public ContactRicardo Tedesco
Faculdade de Medicina de Jundiái
Outcome results
None listed