Breastfeeding, Exclusive Clinical Trial
Official title:
Development of Mobile Application Based Breastfeeding Education Program and Evaluation of the Program Effectiveness
Verified date | August 2022 |
Source | Istanbul University-Cerrahpasa |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Purpose of Research: The purpose of this research is to develop and evaluate the effectiveness of a mobile application-based breastfeeding education program. Research Hypotheses H1: Exclusive breastfeeding rate is higher for mothers in the experimental group than the mothers in the control group in the fourth postpartum week. H2: The mothers in the experimental group had higher scores on the Evaluation of Breastfeeding Problems in the fourth week after delivery than the mothers in the control group. H3: Exclusive breastfeeding rate is higher for the mothers in the experimental group than the mothers in the control group in the eighth postpartum week. H4: The mothers in the experimental group had higher scores on the Evaluation of Breastfeeding Problems at the eighth postpartum week than the mothers in the control group. In the first stage of the research, a mobile application-based breastfeeding education program was developed and piloted. In the second stage of the study, the mobile application-based breastfeeding education program was applied to the primiparous mothers in the experimental group for eight weeks, starting from the first day of postpartum.The control group received only routine health care. 617 / 5.000 Çeviri sonuçları Personal Information Form, Breastfeeding Evaluation Scale and Breastfeeding Problems Evaluation Scale were applied to the mothers in the Experimental and Control groups on the first postpartum day. - A mobile application was installed on the phones of the mothers in the experimental group and information was provided. The control group benefited only from routine nursing care. - Infants' Physical Development Monitoring Form, Breastfeeding Monitoring Form, Breastfeeding Problems Evaluation Scale will be applied to the mothers in the experimental and control groups in the fourth and eighth weeks postpartum. - Mobile Application Evaluation Form was also applied to the experimental group in the eighth week.
Status | Active, not recruiting |
Enrollment | 73 |
Est. completion date | August 1, 2022 |
Est. primary completion date | August 1, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years or older, - Primiparous, - Babies born at term (> 37 weeks of pregnancy or weight > 2500 g) and no health problems that prevent suckling - Planning to breastfeed, - Having a smart phone and effective usage skills, - Mothers who agreed to participate in the study for eight weeks were included in the sample. Exclusion Criteria: - Being the first born, - Having multiple pregnancy, - Having a physical and/or mental health problem - Having a risky newborn, - Having a history of breast surgery or breast reduction. The puerperant women eligible for inclusion in the sampling were assigned to the experimental and control groups by randomization. |
Country | Name | City | State |
---|---|---|---|
Turkey | Istanbul University-Cerrahpasa | Istanbul |
Lead Sponsor | Collaborator |
---|---|
Istanbul University-Cerrahpasa |
Turkey,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | breastmilk exclusive | rate of exclusive breastfeeding for eight weeks | postpartum 1st day- postpartum 8th week | |
Primary | breastfeeding problem | rate of breastfeeding problem eight weeks | postpartum 1st day- postpartum 8th week | |
Primary | baby's physical development | development of baby's weight, height and head circumference | postpartum 1st day- postpartum 8th week |
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