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Problem Solving Problems in Breastfeeding

Phase 2
Conditions
breastfeeding.
Registration Number
IRCT2017070334872N1
Lead Sponsor
Vice chancellor for research, Gonabad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
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

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Breastfeeding self- efficacy. Timepoint: Before the intervention immediately after the intervention and 3 months later. Method of measurement: breastfeeding self-efficacy questionnaire.
Secondary Outcome Measures
NameTimeMethod
Exclusive breastfeeding. Timepoint: Before, immediately after intervention, one and three months later, delivery. Method of measurement: questionnaire.
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