Improving breastfeeding self-efficacy in new mothers
TheEffect of a Solution-FocusedApproach on Breastfeeding Self-efficacy: A RandomizedControlledStudy
This study is testing a new way to help new mothers feel more confident about breastfeeding by focusing on their past successes and positive experiences.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 75 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | Female |
| Sponsor | Eskisehir Osmangazi University Academic / other |
| Locations | 1 site (Eskisehir, Eskişehir) |
| Trial ID | NCT05663567 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a solution-focused approach to enhance breastfeeding self-efficacy among postpartum mothers. It employs a single-blind, randomized controlled design with pre-test and post-test assessments. The intervention aims to address mothers' concerns about breastfeeding through structured sessions that highlight their past achievements and positive experiences. The goal is to improve psychosocial health and alleviate anxiety related to breastfeeding and infant feeding.
Who should consider this trial
Good fit: Ideal candidates are Turkish-speaking, literate, primiparous women who have recently given birth and plan to breastfeed.
Not a fit: Patients who do not wish to breastfeed or have medical conditions preventing breastfeeding will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly boost new mothers' confidence in breastfeeding, leading to better health outcomes for both mothers and infants.
How similar studies have performed: Previous studies utilizing solution-focused approaches have shown promising results in similar contexts, suggesting potential effectiveness in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Over 18 years old, literate, * Can speak Turkish, * Primiparous and at term and healthy delivery (38-42 weeks, 2500-4000g born, 5th minute APGAR score of 7 and above, no known congenital disease), * Women who do not have a chronic disease that prevents breastfeeding in their baby or in themselves * Does not have a systemic disease, * Those who have never received a planned breastfeeding training before, * Having a healthy pregnancy, * Planning to breastfeed, * Women who have internet access, devices with internet usage (smartphone, computer, tablet, etc.), who have Zoom and Google Meet video conferencing applications on these devices. * Women who can be reached within one week at the latest after giving birth Exclusion Criteria: * Women who do not want to breastfeed * Women who have a disability to breastfeed * Expressing that they cannot continue to work until the end, * Women who did not participate and did not answer the post-test of the questionnaires.
Where this trial is running
Eskisehir, Eskişehir
- Eskisehir Osmnagazi Universty — Eskisehir, Eskişehir, Turkey (Recruiting)
Study contacts
- Principal investigator: özlem CAGAN, PHD — ocagan@ogu.edu.tr
- Study coordinator: Esra Nur Kabakci, Phd
- Email: esranurkabakci@gmail.com
- Phone: 02222393750
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.