breastfeeding routin care. Routine postpartum follow-up
Conditions
Interventions
Intervention 1: The control group received two sessions of breastfeeding educational routine care in the health center (before and after delivery). Intervention 2: Interventional group received more t
Prevention
The control group received two sessions of breastfeeding educational routine care in the health center (before and after delivery).
Interventional group received more than routine care two sessions of breastfeeding education before and after delivery from a peer that qualified and full experienced two years of successful breastfee
Sponsors
School of Nursing and Midwifery, Tehran University of Medical Science
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: nulliparous pregnant women; 35-36 weeks gestation (nine months); singleton pregnancy; not having a physical or mental illness; lack of special treatment Interested in participating in a study; the absence of structural defects in the breast; not smoking and alcohol and drug abuse; lack of pregnancy and childbirth complications (hemorrhage and preeclampsia, etc.); have a healthy baby without any congenital defects Exclusion criteria: having a premature baby; needs special care after birth
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Breastfeeding self-efficacy. Timepoint: two months after ending intervention. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Outcome results
None listed