CompletedNot Applicable

Breastfeeding Education and Prenatal & Paternal Attachment

Turkey (Türkiye)101 participantsStarted 2025-01-01

Plain-language summary

This study is designed to evaluate the effect of breastfeeding education on prenatal attachment and paternal attachment among first-time parents. A total of 101 first-time parents (52 in the intervention group and 49 in the control group) will be recruited. Pregnant women will complete the Prenatal Attachment Inventory before and after the intervention, and expectant fathers will complete the Paternal Prenatal Attachment Inventory before and after the intervention. Participants will be selected using non-probability and snowball sampling methods, and the breastfeeding education will be delivered online via Google Meet. The study aims to assess whether structured breastfeeding education can influence prenatal and paternal attachment in first-time parents.

Who can participate

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria:• Primiparous pregnant women * Age 20 years or older * In the second or third trimester of pregnancy * Having internet access Exclusion Criteria Not being a primiparous pregnant woman * Under 20 years of age * Refusal or withdrawal from the education or data collection process * Withdrawal from the study before completing the education * Incomplete pre-test or post-test data * Non-compliance with the study protocol

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Prenatal Attachment

Timeframe: 4 Week

Trial details

NCT IDNCT07154459

SponsorGizem ÇITAK

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-04-01

View on ClinicalTrials.gov More Prenatal Attachment trials

Plain-language summary

Who can participate

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.