Midwife’s supportive care and breastfeeding

INTERVENTION: Control group will receive usual labor and delivery care by staff midwives Experimental group will receive supportive care including physical, educational and emotional support during active phase of labor and also the first hours after delivery by the researcher Intervention 1: Experimental group will receive supportive care including physical, educational and emotional support during active phase of labor and also the first hours after delivery by the researcher. Intervention 2: Control group will receive usual labor and delivery care by staff midwives. Prevention CONDITION: Neonatal difficulty in feeding at breast Neonatal difficulty in feeding at breast. ; Neonatal difficulty in feeding at breast PRIMARY OUTCOME: Onset of lactogenesisII. Timepoint: One weekes after birth. Method of measurement: Questionnaire, checklist. SECONDARY OUTCOME: Exclusive breastfeeding. Timepoint: Six weekes after birth. Method of measurement: Cheklist of daily newborn feeding record. INCLUSION CRITERIA: INCLUSION CRITERIA: primigravida women, gestational age 38‐42 weeks, single foetus, live with cephalic presentation, cervical dilation 3‐4 cm, no medical and obstetric complications and no evidence of foetal distress. Exclusion criteria: Medical complications and congenital malformations in infant