Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Counseling to improve breastfeeding support and outcomes

Official title: The Effect of the Theory-Based Breastfeeding Self-Efficacy Resources Developing Nurse Consultancy Program on Social Support Perception, Breastfeeding Self-Efficacy and Outcomes

Run by Ondokuz Mayıs University · NCT06266806 · Data updated 2026-11-12

This study tests whether a special counseling program can help pregnant women and their families feel more confident about breastfeeding and improve their breastfeeding success.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment100 (estimated)
SponsorOndokuz Mayıs University
Academic / other
Locations1 site (Kars, Center)
StatusRecruiting
StartedJuly 15, 2024
Main results expectedJune 30, 2025
Study endsJune 30, 2025
Registry record updatedMarch 20, 2025
Trial IDNCT06266806 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are pregnant women aged 18 and older, between 28-37 weeks of gestation, who are primiparous and have a supportive relative willing to participate.

Probably not a fit

Patients who may not benefit include those with medical conditions preventing breastfeeding or those who do not have adequate family support.

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

What this trial studies

This study examines the effects of a Nurse Consultancy Program designed to enhance breastfeeding self-efficacy among pregnant women and their family members. Participants will be randomly assigned to either an intervention group, receiving individual counseling based on Breastfeeding Self-Efficacy Theory and hypno-breastfeeding philosophy, or a control group. The intervention consists of five sessions totaling 7.5 hours, focusing on both the mother and her support network. The goal is to improve social support perception and breastfeeding outcomes through targeted education and support.

Why it matters

Potential benefit: If successful, this program could significantly enhance breastfeeding practices and outcomes for mothers and infants.

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

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Being 18 years or older,
* 28-37. be between weeks,
* Being primiparous,
* Having a healthy singleton pregnancy,
* Being at least a primary school graduate,
* Living with his/her spouse,
* There is a relative who will support the mother, whom she defines as a relative (spouse, the woman's mother, or mother-in-law), and this person also agrees to participate in the study,
* There is no condition that prevents breastfeeding for the mother and the baby (medication use, history of any psychiatric or chronic disease, history of any disease in the baby such as cleft palate-lip, etc.),

Exclusion Criteria:

* Not filling out the forms in the study or filling them incompletely,
* The participant wishes to leave the research,
* The emergence of a condition that prevents breastfeeding in the mother and baby,
* Moving from the city where the work is done or moving out of the town,
* Family support is for less than 1 month,

Where it's running

  • Kars Harakani State Hospital
    Kars, Center, Turkey (Türkiye)
    Recruiting

Study contacts

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.