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Successful breastfeeding with inverted nipples

Phase 2
Conditions
Breast-feeding problems.
Neonatal difficulty in feeding at breast
Registration Number
IRCT201512078170N9
Lead Sponsor
Vice Chancellor for Research, Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
99
Inclusion Criteria

Aged between 18-40; willingness of women to participate at study; ability to read and write Persian; infant birth weight between 2000 and 4000 gr; mothers with flat or inverted nipple problem; phone number for follow-up
Exclusion criteria:Using pumps; caps or any other devices to facilitate breastfeeding; mothers' infants with physiological; anatomical and other abnormalities no able to feed orally; history of physical and mental illness of the mother (epilepsy; gastrointestinal disorders; cardiovascular; kidney); having stressful accidents 1 month ago such as divorce; death of family members; using effective drugs during breastfeeding (to increase and decrease milk and hormones); presence of a disease or disorder affecting the attachment of the baby on mother

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The number of infants’ breast-feeding. Timepoint: 1, 7, 15. Method of measurement: Device for weight gain.;Comparing the number of infants’ breast-feeding during 1, 7 and 15 days at massage group. Timepoint: 1 , 7 and 15. Method of measurement: Calculating the number of infants’ breast-feeding and device for weight gain.;Comparing the number of infants breast-feeding during 1, 7 and 15 days at 3 groups. Timepoint: 1, 7 , 15. Method of measurement: Calculating the number of infants’ breast-feeding and device for weight gain.
Secondary Outcome Measures
NameTimeMethod
Mother-infant bounding. Timepoint: Day 1 and 15 after intervention. Method of measurement: Maternal-fetal bounding scale.;Determining the frequency of adverse events in mother and infant at groups of study. Timepoint: 1-14 after intervention. Method of measurement: Self- designed check List.
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