The Effect of Telephone Support for Breastfeeding Follow-up on Infantile Colic and Maternal Breastfeeding Self-efficacy
Breastfeeding, Exclusive, Infantile Colic, Self Efficacy
About this trial
This is an interventional supportive care trial for Breastfeeding, Exclusive
Eligibility Criteria
Inclusion Criteria:
- Having / had a new birth between the ages of 18-45
- Having his 1st or 2nd birth
- Agreeing to participate in the study voluntarily and obtaining consent form
- Having given birth to a healthy baby above 36 weeks of gestation
- Planning to breastfeed
- The baby does not need intensive care and does not develop any postpartum complications
- The baby does not have a vision and hearing problem, does not have a disease that may prevent breastfeeding
- The baby does not have a physical and psychological deficit
- The baby does not have a disease or an anatomical problem that will prevent breastfeeding
- Mother's ability to continue monitoring on the phone and to have a phone that can provide monitoring and video chat.
- No blood incompatibility between mother and baby.
Exclusion Criteria:
- Refusal to participate in the study
- Failure to continue monitoring by phone
- Mother's illiteracy
- Development of pathological jaundice in the baby
Sites / Locations
- Gülçin Özalp Gerçeker
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Study group/Telephone support for breastfeeding follow-up
Control Group
Study group: The women in the study group will be provided with a video call every day for the first week after discharge from the hospital, to provide consultancy to the mother on the matters she needs and to be recorded in the Baby Monitoring Form. The general appearance of the baby, observation during sucking, jaundice, drowsiness, reluctance to suck will be observed. The consultancy will be provided to the mother on these issues. In the following weeks, the consultancy will continue to be given to the study group by making a video talk one week apart. The researcher's phone will be given to the mothers in both groups and the incoming calls and their content will be recorded.
Control Group: No additional attempt or routine call will be made to mothers in the control group. The researcher's phone will be given to the mothers in both groups and the incoming calls and their content will be recorded. The control group will be called to fill in the scales for monitoring purposes.