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Clinical Trials in Turkey / NCT07461428
Enrolling by invitation Not applicable

Evaluation of the Effectiveness of a Hypnobreastfeeding Education Program Based on the ınformation-Motivation-Behavioral Skills Model in Primiparous Women

NCT07461428 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-05-20
Last updated
2026-09-01

Condition(s) studied

HypnoBreastfeedingBreastfeeding EducationPregnancyHealthy

Investigational drug(s) / intervention(s)

breastfeeding education program based on hypnobreastfeeding philosophy

breastfeeding education program based on hypnobreastfeeding philosophy: Hypnobreastfeeding training and counseling will be provided by a researcher with certifications in Mindfulness and Self-Compassion Skills Development. The Hypnobreastfeeding Philosophy-Based Breastfeeding Training Program is planned for weeks 28-32 of pregnancy.The training will cover topics such as 'My dream breastfeeding, meeting information needs related to breastfeeding'. The first training session will last a total of 120 minutes.The second training session will be held in week 30 of pregnancy. In the second training session, topics such as mulberry meditation for conscious breastfeeding, affirmations for breastfeeding and Dr. Masaru Emoto's "The Effect of Thoughts on Water Molecules" experiment, emotional awareness exercise, Alfred and his shadow: a short film about emotions, feelings and emotions related to breastfeeding and the relationship between hormones and emotions: oxytocin and endorphin massage will be covered.

Study summary

This randomized controlled trial aimed to evaluate the effectiveness of an education program based on the Information-Motivation-Behavioral Skills (IMB) Model and grounded in the philosophy of hypnobreastfeeding provided to primiparous pregnant women.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * • Aged 18 years or older, * At least primary school graduates, * Between 27 and 28 weeks of gestation, * Primiparous, * Without high-risk pregnancies (e.g., gestational diabetes, epilepsy, preeclampsia, multiple pregnancy, etc.), * Without pre-existing health conditions prior to pregnancy (e.g., diabetes mellitus, hypertension, renal failure, epilepsy, etc.), * Without diagnosed psychiatric disorders (e.g., anxiety, mood disorders, depression, bipolar disorder, etc.), * Willing to participate voluntarily in the prenatal education program, * Not previously enrolled in a structured breastfeeding education program, * Turkish-speaking and without any communication barriers (e.g., cognitive, hearing, or visual impairments), * Not a member of a health sciences profession, and * Having access to the internet, a computer, or a smartphone. Exclusion Criteria: * • Incomplete completion of data collection forms, * Withdrawal from participation in the study, * Failure of pregnant women in the intervention group to fully participate in the educational program, * Lack of internet access, * Prior participation in a structured breastfeeding education program, * Discontinuation of breastfeeding by the mother after delivery, and * Any circumstances that would prevent the breastfeeding process or require mother and infant to be separated.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Ankara Yildirim Beyazit Üniversitesi Esenboğa Külliyesi Ankara Esenboğa
Sivas Cumhuriyet Üniversitesi Sağlik Hizmetleri Uygulama Ve Araşturma Hastanesi Sivas Merkez

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07461428 on ClinicalTrials.gov ↗ ← All trials in Turkey