Status:
NOT_YET_RECRUITING
The Effect of Artificial Intelligence Supported and Nurse-Led Online Breastfeeding Counseling
Lead Sponsor:
Kafkas University
Conditions:
Artificial Intelligence
Nursing Caries
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
Breastfeeding is the gold standard in infant nutrition in the first 12 months of life (1). Breastfeeding self-efficacy perception is one of the most important factors affecting mothers\' breastfee...
Detailed Description
Breastfeeding positively affects mother-infant bonding (5). Breast milk is the healthiest food source for the nutrition and development of the newborn (6). Mortality and morbidity rates from infectiou...
Eligibility Criteria
Inclusion
- The pregnant woman is willing to participate in the research,
- The pregnant woman must have an informed written voluntary consent form,
- The pregnant woman is over 18 years of age,
- The pregnant woman speaks and understands Turkish,
- Having the pregnant woman\'s first baby (primiparous),
- The pregnant woman is planning to give birth in the hospital where she came for pregnancy check-up,
- The pregnant woman must have received breastfeeding training at the family health center to which she is affiliated.
- The baby does not have a disease that would prevent sucking (cleft palate, cleft lip, etc.),
- The baby is born older than the 37th week of pregnancy,
- The baby\'s birth weight is 2500 g and above, and the APGAR score is 7 and above at the 5th minute.
Exclusion
- The pregnant woman has mental retardation that affects her ability to understand and comprehend,
- Multiple pregnancy,
- The pregnant woman has gestational disorders such as preeclampsia, eclampsia and a history of gestational diabetes,
- The pregnant woman has a diagnosed psychiatric disorder,
- The pregnant woman receives support from a private breastfeeding consultant,
- Taking the baby to the neonatal intensive care unit after birth,
- The baby is born before the 37th week of pregnancy,
- Loss of communication with pregnant women who were contacted before birth, after birth,
- Pregnant women who do not use smartphones,
- Pregnant women who have an application installed on their phones but have never used the application until the birth,
- Pregnant women who were given an educational booklet but did not look at the booklet until the birth,
- Pregnant women who do not attend the 1.5-hour training or who have to leave the training halfway will be excluded.
Key Trial Info
Start Date :
September 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2025
Estimated Enrollment :
90 Patients enrolled
Trial Details
Trial ID
NCT06569017
Start Date
September 1 2024
End Date
December 1 2025
Last Update
August 23 2024
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