Self Efficacy Clinical Trial
Official title:
The Effect of Telephone Support for Breastfeeding Follow-up on Physiological Jaundice, Exclusive Breastfeeding in the First Six Months, Infantile Colic, Maternal Breastfeeding Self-efficacy, and Breastfeeding Success
NCT number | NCT04632888 |
Other study ID # | 5762-GOA |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 14, 2020 |
Est. completion date | May 30, 2021 |
Verified date | February 2022 |
Source | Dokuz Eylul University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study was planned to examine the effect of telephone support for breastfeeding follow-up on physiological jaundice, exclusive breastfeeding in the first six months, infantile colic, maternal breastfeeding self-efficacy, and breastfeeding success.
Status | Completed |
Enrollment | 70 |
Est. completion date | May 30, 2021 |
Est. primary completion date | May 30, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
Turkey | Gülçin Özalp Gerçeker | Izmir |
Lead Sponsor | Collaborator |
---|---|
Dokuz Eylul University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | breastfeeding success | LATCH Breastfeeding Assesment Scale: It is a measurement tool developed to evaluate breastfeeding. It was created to diagnose breastfeeding, to identify problems, to determine training accordingly, to create a common language among health professionals and to be used in studies. This measurement tool consists of the English initials of five evaluation criteria. Each item is scored between 0-2 points. The highest score is 10. | until discharge from the hospital an average 2 week | |
Primary | Infantile Colic | Infantile Colic Scale: It was developed to diagnose and evaluate colic. The validity and reliability study of the scale was done in Turkey. 12 Scale items are graded with Likert type scoring ranging from 1 to 6. | until discharge from the hospital an average 24 week | |
Primary | Maternal Breastfeeding Self-Efficacy | Breastfeeding Self-Efficacy Scale-Short Form: It is a 33-item scale to evaluate breastfeeding self-efficacy levels of mothers. Later, a 14-item short form of the scale was developed in 2003. It is applied more easily and evaluates self-efficacy correctly. Breastfeeding Self-Efficacy Short Form Scale is a 5 point Likert type scale. | until discharge from the hospital an average 24 week | |
Primary | rate of physiological jaundice | physiological parameter of jaundice | until discharge from the hospital an average 2 week | |
Primary | rate of exclusive breastfeeding | exclusive breastfeeding for 6 months | until discharge from the hospital an average 24 week |
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