breastfeeding.
Conditions
Interventions
Intervention 1: Intervention in the test group of problem solving skills by lecture method in six sessions of the first session. Familiarization and completion of demographic questionnaires, lactation
Lifestyle
In this study, the control group does not receive any intervention.
Intervention in the test group of problem solving skills by lecture method in six sessions of the first session. Familiarization and completion of demographic questionnaires, lactation, lactation self
Sponsors
Vice chancellor for research, Gonabad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Major entry into the study: first and secondarily pregnancy; having at least elementary education; lack of prediction of lactation premature delivery; Not having known known problems affecting breastfeeding for mother and fetus; having satisfaction to participate in a study; being exposed to psychological social stress ((serious illness or spouse, one's relatives' death, immigration, acute economic conditions, marital divorce and Accident)); Main departure conditions: Low birth weight and preterm labor; having a baby in conditions that cause lacrimation disorders such as cleft palate, lacrimal gastric ulcer and etc; fetal death or mother during the intervention; mother's being infected with known diseases The physical and mental impairment of lactation; the use of certain medications that are effective in breastfeeding (bromocriptine, primidone, doxorubicin, marbroate and other drugs that are contraindicated in breastfeeding); admission of breastfeeding in hospital or separation from mother during study; accidents Harsh and stressful (serious illness or spouse, one's close relatives, immigration, acute economic conditions, big differences in women Overshoot and accident) during the study; Breast problems in the breach of breastfeeding, absenteeism and more mother; desire to leave the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Breastfeeding self- efficacy. Timepoint: Before the intervention immediately after the intervention and 3 months later. Method of measurement: breastfeeding self-efficacy questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Exclusive breastfeeding. Timepoint: Before, immediately after intervention, one and three months later, delivery. Method of measurement: questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtefeh Abbazaadeh
Gonabad Medical Sciences
Outcome results
None listed