Clinical trial Recruiting at 1 site Interventional Ages 15 to 35 Women only

Breastfeeding support program for first-time mothers

Official title: 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

Run by Pamukkale University · NCT06446362 · Data updated 2026-11-12

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

Study typeInterventional
Ages15 Years to 35 Years
SexWomen only
Enrollment45 (estimated)
SponsorPamukkale University
Academic / other
Locations1 site (Denizli, Pamukkale)
StatusRecruiting
StartedDecember 1, 2024
Main results expectedSeptember 1, 2026
Study endsDecember 1, 2026
Registry record updatedNovember 19, 2024
Trial IDNCT06446362 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a 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.

Probably not a fit

Patients who may not benefit include those with medical complications that hinder breastfeeding or infants with health issues.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

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 gone: Other studies have shown positive outcomes with similar breastfeeding support approaches, indicating potential for success in this trial.

Who can join: the full rules

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 it's running

  • Pamukkale University Family Health Center
    Denizli, Pamukkale, Turkey (Türkiye)
    Recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.