None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The subjects of this study are pregnant women who are scheduled for epidural anesthesia with a non-administrative method that does not include a narcotic analgesic (fentanyl state) during delivery and are expected to have a normal vaginal delivery under medical interventions such as administration of uterine contractions (oxytocin). The specific selection criteria are those who are more than 37 weeks pregnant and have healthy fetuses with parietal fetuses, those who are expected to have a normal vaginal delivery by an obstetrician, and those who do not fall under the prohibition in the Physical Activity Readiness Medical Examination for Pregnancy (PARmed-X).
Exclusion criteria
Exclusion criteria: Exclusion criteria are those who have been diagnosed with amniotic fluid hyperplasia, amniotic fluid hyperplasia, those who have one or more exercise contraindications, and those who regularly participate in exercise programs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| labor time; type of delivery;Apgar scores of newborns;neonatal oxygen therapy;birth satisfaction | — |
Countries
Korea, Republic of
Contacts
Dong-eui University