The World Health Organization (WHO) states that peer support breastfeeding education programs are effective interventions for improving breastfeeding outcomes. In this context, the WHO's Global Strategy for Infant and Young Child Feeding recommends the implementation of "lay health worker peer counselors" and "mother-to-mother support groups" to promote and support breastfeeding. The tenth step of the Baby-Friendly Hospital Initiative also emphasizes the importance of mother-to-mother support as a successful intervention for breastfeeding. However, in our country, there have been limited studies and efforts to provide peer education and support for breastfeeding. Although various valuable studies using different educational techniques have been conducted to improve breastfeeding rates, the integration of these programs into routine clinical practice remains insufficient. This study aims to implement a peer interactive education program in postpartum rooms to bring experienced and inexperienced mothers together, as part of the hospital routine. The project will focus on the development and implementation of a peer interactive education program and will investigate its impact on the breastfeeding self-efficacy of primiparous mothers. The research follows a two-group pre-test and post-test design, is non-blind, and uses randomized controlled methodology. Initially, the hospital rooms will be rearranged to accommodate the implementation of the peer support breastfeeding education module. Researcher midwives will provide a brief training to experienced peer educator mothers who have previously breastfed.Afterwards, the peer education program will be conducted when the experienced mother and primiparous mother are together in the room. The study emphasizes improving early postpartum breastfeeding success and aims to make peer interaction a routine part of hospital practice. The feasibility of implementing peer education in hospitals will be evaluated, considering its simplicity and practicality. The impact of peer interactions on the mother's breastfeeding self-efficacy and attitudes towards breastfeeding will be assessed.

Overall, this research aims to improve breastfeeding rates by implementing peer support programs in hospital settings and evaluating the outcomes of peer interactions in terms of the mother's breastfeeding self-efficacy and attitudes towards breastfeeding.

Study Design: This project was planned as a two-group, non-blinded randomised controlled trial.

Ethical approval was obtained from the Medical Research Ethics Committee of a university for the conduct of the study (Date: 08.11.2022, Decision no: 22-11T/25).

Population and Sample of the Study: Mothers who were hospitalised in Izmir Democracy University Buca Seyfi Demirsoy Training and Research Hospital obstetrics and gynaecology ward, who met the inclusion criteria and volunteered to participate in the study will constitute the population of the study. A priori power analysis was performed using G.Power 3.1.9.2 package programme to determine the sample size. In the calculation made, with the assumption of 0.5 effect value for 80% power at 95% confidence interval, it was calculated as 128 women, 64 for the group in which peer supported breastfeeding education will be applied and 64 for the group in which standard education will be applied. In order to ensure homogeneity between the groups and to eliminate selection bias, the "block randomisation" method, one of the fixed probability randomisation methods, will be used in the study and women who meet the inclusion criteria will be distributed to the intervention and control groups.

Hypotheses of the study

1. H1: Breastfeeding self-efficacy of mothers who receive peer interaction after birth will be higher than the control group.
2. H1: The level of exclusive breastfeeding of mothers receiving peer interaction will be higher than that of mothers in the control group.

Mothers to provide peer support

• Multipar
• Mothers with successful breastfeeding experience (Exclusive breastfeeding of the previous baby for at least 6 months, continued breastfeeding at the age of 2 years or older)
• At least secondary education graduate
• Singleton birth
• Vaginal birth (due to rapid mobilisation after birth and quicker adaptation to daily activities)
• with a child aged 5 years and under (limit for the age of the previous child for the memory factor regarding breastfeeding experience)
• Breastfeeding self-efficacy scale score of 60 and above (out of a total score of 70)
• No known or diagnosed psychiatric health problem in medical history
• Women without any health problem that may prevent breastfeeding will be included.

Intervention-Control group mothers

• Primipar
• 18 years and over
• Singleton birth
• No known or diagnosed psychiatric health problem in medical history
• Women who do not have any health problems that may prevent breastfeeding will be included.

Baby

• Born between 37-42 weeks
• Birth weight ≥2.5 kg and ≤3.9 kg
• 1 and 5 minute Apgar scores ≥8
• Not referred to neonatal intensive care unit

Exclusion criteria for individuals/patients in the study:

• Under 18 years of age
• Non-literate in Turkish
• Has a psychiatrically diagnosed health problem
• Developing a health problem that may prevent breastfeeding
• Taking medication that may jeopardise breastfeeding
• Women who do not want to participate will not be included in the study.

Exclusion criteria

• Requesting a room change
• Not wanting to/wanting to stop peer interaction within the scope of the room arrangement
• After settling in the room, those who did not want to answer the data collection tools for any reason/left the data collection tools unfinished
• Mothers who could not be reached in the postnatal 1st month follow-up will be excluded from the study.

When the study is completed, the study protocol and data can be shared with other researchers.

When the work is completed

not yet identified

In order to eliminate selection bias in the study, "block randomisation" method, one of the fixed probability randomisation methods, will be used and women who meet the inclusion criteria will be distributed to the intervention and control groups.