NCT06266806 The Effect of Breastfeeding Counseling on Social Support Perception, Breastfeeding Self-Efficacy and Outcomes
| NCT ID | NCT06266806 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Ondokuz Mayıs University |
| Condition | Breastfeeding, Exclusive |
| Study Type | INTERVENTIONAL |
| Enrollment | 100 participants |
| Start Date | 2024-07-15 |
| Primary Completion | 2025-06-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 100 participants in total. It began in 2024-07-15 with a primary completion date of 2025-06-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The purpose of this study is to examine the effects of the Breastfeeding Self-Efficacy Resources Development Nurse Consultancy Program (EMÖZGEDAP), based on Dennis's Breastfeeding Self-Efficacy Theory along with the hypno-breastfeeding philosophy given to mothers and family relatives, on social support perception, breastfeeding self-efficacy and outcomes. The study will involve pregnant women and close others assigned randomly to the intervention (n=50) or control (n=50) groups in a state hospital in Turkey. Individual counseling will be provided to the intervention group within the scope of the EMÖZGEDAP, based on Denis's Breastfeeding Self-Efficacy theory and hypnobreastfeeding philosophy. EMÖZGEDAP, which will be applied to pregnant women and their family relatives, will consist of 5 sessions lasting 7.5 hours (2 sessions with the woman and her family relatives, two sessions with the woman alone, and one with her family relatives alone). The Antenatal Breastfeeding Self-Efficacy Scale will be evaluated before the counseling program is given in the antepartum period. Breastfeeding and Nutrition Results, Postpartum Breastfeeding Self-Efficacy Scale, Breastfeeding Self-Efficacy Scale for Fathers, Assessment Scale for Perceived Support of Close Others in Relation to Breastfeeding Self-Efficacy and Scale of Perception of Close Others' Support For Breastfeeding Self-Efficacy will be evaluated at the 1st, 3rd, and 6th months postpartum.
Eligibility 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,
Contact & Investigator
Özen KULAKAÇ, Professor
STUDY DIRECTOR
Ondokuz Mayıs University
Frequently Asked Questions
Who can join the NCT06266806 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Breastfeeding, Exclusive. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06266806 currently recruiting?
Yes, NCT06266806 is actively recruiting participants. Contact the research team at humeyra.tulek@gmail.com for enrollment information.
Where is the NCT06266806 trial being conducted?
This trial is being conducted at Kars, Turkey (Türkiye).
Who is sponsoring the NCT06266806 clinical trial?
NCT06266806 is sponsored by Ondokuz Mayıs University. The principal investigator is Özen KULAKAÇ, Professor at Ondokuz Mayıs University. The trial plans to enroll 100 participants.