Delivery. Single spontaneous delivery
Conditions
Interventions
Intervention 1: Intervention group: The subjects in this group will receive evidence based care during normal labor and delivery. Intervention 2: Control group: This group will be received routine car
Intervention group: The subjects in this group will receive evidence based care during normal labor and delivery
Control group: This group will be received routine care of hospital during normal labor and delivery
Sponsors
Isfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: intend to participation in study; low risk pregnant women; maternal age 18-35 years old; single pregnancy; gestational age 38-42 weeks; vertex presentation; spontaneous labor pain; vaginal dilatation between 3 and 4 centimeter; mother BMI 19.8-26 kg/m2; estimated fetal weight 2500-4000 gr. Exclusion criterion: unwillingness or reject of participation in study
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of active phase and second stage of labor. Timepoint: Cervix dilatation from 4 centimeter to 10 centimeter for active phase of labor and cervix dilatation from 10 centimeter to delivery of newborn for second stage of labor. Method of measurement: Clinical examination/ Measurement by digital chronometer / record in check list.;Labor Pain intensity. Timepoint: Measurement severity of pain during first and second stage of labor. Method of measurement: By visual analog scale/ record in check list.;Frequency use of oxytocin during normal labor. Timepoint: During first and second stage of normal labor. Method of measurement: Observation / record in check list.;Frequency use of routine episiotomy. Timepoint: Before of delivery. Method of measurement: Observation and record in check list.;Post partum hemorrhage. Timepoint: After childbirth. Method of measurement: Measurement of HG and HCT level by blood sampling 12 and 24 h after childbirth.;Spontaneous tears in perinea and vagina. Timepoint: After of delivery. Method of measurement: Observation / clinical examination/ record in check list.;Method of delivery. Timepoint: After of delivery. Method of measurement: Observation and record in check list.;Mother’s satisfaction of delivery. Timepoint: Before discharging of hospital. Method of measurement: Macky satisfaction questionnaire.;Apgar score. Timepoint: 1 and 5 minute after of delivery. Method of measurement: Observation and record in check list.;Frequency newborn admission to neonatal ward or NICU. Timepoint: After of delivery. Method of measurement: Observation and record in check list.;Breast feeding during 30 min after birth. Timepoint: during30 min after birth. Method of measurement: Observation and record in check list.;Average time of admission to discharge of mother. Timepoint: Of admission time to discharge. Method of measurement: Measurement by Digital chronometer / record in check list. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMina Iravani
Isfahan University of Medical Sciences, Nursing and Midwifery School
Outcome results
None listed