Peer support program for new mothers to improve breastfeeding
The Effect of Peer Interaction on Breastfeeding Self-Efficacy of Primiparas Sharing the Same Room With Mothers With Successful Postpartum Breastfeeding Experience; Randomised Controlled Study
This study tests whether pairing new mothers with experienced moms for support can help them breastfeed better than just standard education.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 128 (estimated) |
| Ages | 18 Years to 49 Years |
| Sex | Female |
| Sponsor | Ege University Academic / other |
| Locations | 1 site (Izmir) |
| Trial ID | NCT06277856 on ClinicalTrials.gov |
What this trial studies
This study implements a peer interactive education program in postpartum rooms, pairing experienced mothers with new mothers to enhance breastfeeding outcomes. It is designed as a randomized controlled trial with two groups: one receiving peer support and the other receiving standard education. The study aims to assess the impact of peer interaction on breastfeeding self-efficacy and exclusive breastfeeding rates among participants. Ethical approval has been obtained, and a power analysis determined a sample size of 128 women for the trial.
Who should consider this trial
Good fit: Ideal candidates include first-time mothers aged 18 and over who have had a singleton vaginal birth and no health issues preventing breastfeeding.
Not a fit: Patients who may not benefit include those with psychiatric health problems or those who have had complications during childbirth that affect breastfeeding.
Why it matters
Potential benefit: If successful, this program could significantly improve breastfeeding rates and self-efficacy among new mothers.
How similar studies have performed: Previous studies have shown that peer support programs can effectively improve breastfeeding outcomes, indicating a promising approach.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Izmir
- Ege University — Izmir, Turkey (Recruiting)
Study contacts
- Principal investigator: Aysun Eksioglu, Assoc Prof — Ege University
- Study coordinator: Aysun Ekşioğlu, Midwife
- Email: aysun.basgun@ege.edu.tr
- Phone: +905054993214
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.