Design, Implementation and Evaluation of a plan for Labor and Normal Delivery.
Conditions
Interventions
Intervention 1: Intervention group: In the intervention group of the Department of Labor and Natural Birth, it will be performed by trained midwives based on the evidence-based designed program. Inter
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 49 Years
Inclusion criteria
Inclusion criteria: Consent to participate in the study primiparous women singleton pregnancy live fetus maternal age 15-49 years gestational age 37 to 42 weeks (based on the first day of the last menstrual period or first trimester ultrasound) cephalic presentation normal fetal heart rate (110 -160)
Exclusion criteria
Exclusion criteria: history of any incision on the uterus - detection of abnormal dimensions of the pelvis through vaginal examination and examination of ischial spines, obstetric conjugation, sacrum concavity, condition of pelvic wall(s) and pubic arch angle abnormal bleeding epidural anesthesia presence of any abnormalities in soft tissue or Bony birth canal (diagnosed through vaginal examination) having an abnormal fetus or intrauterine growth restriction indication for cesarean section (fetal distress, prolapse of the umbilical cord, diagnosis of absolute pelvic stenosis by the doctor) known medical diseases based on the patient's file including history or current suffering from any systemic disease such as diabetes, high blood pressure, heart disease, kidney disease, nervous disease, liver disease, digestive disease, respiratory disease, thyroid disease) Fetal membranes that have been ruptured for more than 8 hours High-risk pregnancy (preeclampsia, placenta previa, Placental abruption, chorioamnionitis, placenta accreta)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Type of delivery. Timepoint: after the study. Method of measurement: Questionnaire.;Satisfaction with childbirth. Timepoint: after the study. Method of measurement: Mackey questionnaire.;Childbirth Experience. Timepoint: after the study. Method of measurement: Childbirth Experience Questionnaire.;The pain of childbirth. Timepoint: During the study. Method of measurement: Visual Analogue Scale.;The length of labor stages. Timepoint: During the study. Method of measurement: Check list.;Apgar first and fifth minutes. Timepoint: After the intervention. Method of measurement: check list.;Hospitalization in the neonatal intensive care unit. Timepoint: After the intervention. Method of measurement: check list.;Postpartum bleeding. Timepoint: During the study. Method of measurement: check list.;Genital lacerations. Timepoint: During the study. Method of measurement: check list. | — |
Secondary
| Measure | Time frame |
|---|---|
| Early breastfeeding. Timepoint: During the study. Method of measurement: check list. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactmina iravani
Ahvaz University of Medical Sciences
Outcome results
None listed