Breastfeeding, Self Efficacy
Conditions
Keywords
Breastfeeding Roadmap
Brief summary
The effect of the breastfeeding roadmap used in primiparous mothers on breastfeeding self-efficacy perception and breastfeeding success will be evaluated.
Detailed description
The research was planned as a randomized controlled experimental study. Mothers who meet the inclusion criteria and agree to participate in the study will be assigned to the intervention and control groups according to the randomization list. A total of 74 primiparous mothers who gave birth, 37 in the intervention group and 37 in the control group, will be included in the study. In addition to the routine breastfeeding education given by the clinic's education nurse, the mothers in the intervention group will also receive a Breastfeeding Roadmap education poster prepared by the researchers, which will be hung on the wall of their rooms. The researcher will introduce the Breastfeeding Roadmap to the mothers and provide information on breastfeeding. Routine hospital breastfeeding education will receive to mothers in the control group after childbirth. Data Collection Pre-Test; Introductory Information Form, Breastfeeding Self-Efficacy Scale Short-Form, LATCH Breastfeeding Assessment Tool will be collected within the first hour after birth (before Breastfeeding Roadmap breastfeeding education and hospital routine breastfeeding education were implemented) Post-test; Breastfeeding Self-Efficacy Scale Short-Form, LATCH Breastfeeding Assessment Tool will be collected at least two hours before mothers are discharged from the hospital (the discharge period usually varies between 24 and 48 hours). At the end of the study, the results of the mothers in the experimental and control groups will be evaluated.
Interventions
OTHERBreastfeeding Education with Breastfeeding Roadmap
Information about the Breastfeeding Roadmap prepared by the researchers will be explained to the mothers in the intervention group and hung in poster rooms.
Sponsors
Selcuk University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Volunteer to participate in the study, * Primiparous, * Giving birth at 37 weeks of gestation or later, * No condition preventing breastfeeding, * No condition preventing breastfeeding in the baby, * At least primary school graduate, * Mothers aged 18 and over
Exclusion criteria
* Those who have given birth to multiple pregnancies, * Those who received general anesthesia for Caesarean section, * Those who have any chronic disease, diagnosed mental or psychiatric illness history, * Those who have a history of preeclampsia, eclampsia and gestational diabetes, * Those whose babies are in intensive care after birth
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Sociodemographic characteristics | Within the first hour after the mother's birth. | Comparison of sociodemographic characteristics of women before the intervention with the questionnaire |
| Breastfeeding Self-Efficacy Short Form Scale | Within the first hour after the mother's birth. | Mothers whose pre-test data are collected will be assigned to intervention and control groups (Pre-test). The scale consists of 14 items. It is scored between 1-5 and the lowest 14 and the highest 70 points can be obtained. The higher the score obtained from the scale, the higher the breastfeeding self-efficacy. |
| LATCH Breastfeeding Assessment Tool | Within the first hour after the mother's birth | Mothers whose pre-test data are collected will be assigned to intervention and control groups (pre-test). The scale consists of five evaluation criteria and each item is evaluated between 0-2 points. The score that can be obtained from the measurement tool can vary between 0-10. The higher the score obtained from the scale, the higher the breastfeeding success. |
Countries
Turkey (Türkiye)
Outcome results
None listed