Effects of consultation based on Bristol tool on breast-feeding
Not Applicable
- Conditions
- Breast- feeding disorders among mothers undergoing Cesarean section.Other and unspecified disorders of breast associated with childbirth
- Registration Number
- IRCT2017041810426N16
- Lead Sponsor
- Hamadan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
Cesarean section delivery; primiparous; literacy; Residency in Hamadan city; Having a mobile number for follow-ups; Singleton birth and term delivery. Exclusion criteria: Inability to do breastfeeding according to physician’s approval; Problems after cesarean section such as bleeding and anesthesia related problems; Underlying disease in mother such as cardiac, pulmonary, chronic and infection diseases; Addiction; Neonatal abnormality and diseases.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mother's self-efficacy in breastfeeding. Timepoint: 2 hours after delivery, second day after delivery, 7 to 10 days after delivery, one month after delivery and four months after delivery. Method of measurement: Breastfeeding Self-Efficacy.
- Secondary Outcome Measures
Name Time Method Maintaining of exclusive breastfeeding. Timepoint: 2 hours after delivery, second day after delivery, 7 to 10 days after delivery, one month after delivery and four months after delivery. Method of measurement: Breast-feeding checklist.