CompletedNot Applicable

The Effect of Breastfeeding Education Given by Pecha Kucha Method

Turkey (Türkiye)75 participantsStarted 2024-07-11

Plain-language summary

To evaluate the effect of breastfeeding education given with Pecha Kucha method in the prenatal period on breastfeeding self-efficacy, infant feeding attitude and breastfeeding satisfaction in the postpartum period.

Who can participate

Age range

18 Years – 60 Years

Sex

FEMALE

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: * Volunteered to participate in the research, * To be able to speak and understand Turkish, * Over 18 years of age, * At least primary school graduate, * Gestational week 38 weeks and above * No chronic illness, * Pregnant women without communication barriers will be included in the study. Exclusion Criteria: * Have a medical indication that prevents breastfeeding, * Multiple pregnancies, * A person with a mental illness, * Not wanting to continue the research process, * The one who still hasn't given birth 2 weeks after the training, * Not having their baby with them after childbirth, * Pregnant women who cannot be reached during the follow-up period will be excluded from the study

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

Antenatal and Pospartum Breastfeeding Self-Efficacy Scale Short Form

Timeframe: 0,2 and 4 weeks

Trial details

NCT IDNCT06528782

SponsorSaglik Bilimleri Universitesi

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-09-11

View on ClinicalTrials.gov More Breast Feeding trials