Breastfeeding support program for first-time mothers
The Effect of an Interaction Model of a Client Health Behavior-Based Breastfeeding Support Program on Breastfeeding Self-Efficacy, Attitudes, and Problems in Primiparous Mothers: A Randomized Controlled Trial
This study is testing a new breastfeeding support program for first-time mothers to see if it helps them feel more confident and positive about breastfeeding compared to regular care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 45 (estimated) |
| Ages | 15 Years to 35 Years |
| Sex | Female |
| Sponsor | Pamukkale University Academic / other |
| Locations | 1 site (Denizli, Pamukkale) |
| Trial ID | NCT06446362 on ClinicalTrials.gov |
What this trial studies
This randomized controlled trial aims to evaluate the effects of a client health behavior interaction model-based breastfeeding support program on breastfeeding self-efficacy, attitudes, and challenges faced by first-time mothers. Participants will receive structured support and undergo assessments at various intervals to measure changes in their breastfeeding confidence and attitudes. The study will compare outcomes between mothers receiving the intervention and those receiving standard care, providing insights into the effectiveness of the program.
Who should consider this trial
Good fit: Ideal candidates for this study are primiparous mothers between 32 and 40 weeks of gestation who can communicate effectively and own a smartphone.
Not a fit: Patients who may not benefit include those with medical complications that hinder breastfeeding or infants with health issues.
Why it matters
Potential benefit: If successful, this program could significantly enhance breastfeeding self-efficacy and attitudes among first-time mothers, leading to improved breastfeeding practices.
How similar studies have performed: Other studies have shown positive outcomes with similar breastfeeding support approaches, indicating potential for success in this trial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Primiparous mothers * Gestational age between 32-40 weeks * Ability to communicate effectively * Ownership of a smartphone * Minimum education level: primary school graduate Exclusion Criteria: * Infants with health issues * Mothers with medical or pregnancy-related complications that hinder breastfeeding (e.g., heart disease, cancer, nephritis, active or untreated tuberculosis, HIV/AIDS, active herpes lesions on the breast, severe malnutrition) * Participants undergoing infertility treatment with IVF
Where this trial is running
Denizli, Pamukkale
- Pamukkale University Family Health Center — Denizli, Pamukkale, Turkey (Türkiye) (Recruiting)
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.