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Clinical Trials in Turkey / NCT07415122
Starting soon Not applicable

The Effect of Mindfulness-Based Childbirth Education on Fear of Birth, Prenatal Stress, and Childbirth Self-Efficacy

NCT07415122 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-02-01
Last updated
2026-02-18

Condition(s) studied

Prenatal StressChildbirth Self-efficacyFear of Childbirth

Investigational drug(s) / intervention(s)

Mindfulness-based childbirth preparation education

Mindfulness-based childbirth preparation education: This intervention consists of a structured childbirth preparation education program that integrates mindfulness practices into routine antenatal education. The program includes breathing exercises, body awareness activities, mindful relaxation, and guided meditation. The intervention is delivered in group sessions by a trained midwife, with four sessions conducted over a two-week period. The content is designed to reduce fear of childbirth, decrease prenatal stress, and enhance childbirth self-efficacy.

Study summary

This randomized controlled trial aims to evaluate the effect of mindfulness practices integrated into childbirth preparation education on fear of childbirth, prenatal stress, and childbirth self-efficacy in pregnant women.Participants will be randomly assigned either to the childbirth education group with mindfulness practices or to the standard childbirth education/control group. Results will be evaluated using the prenatal self-assessment childbirth fear subscale, the perceived stress scale before childbirth, and the self-efficacy scale during labor before and after intervention.This study aims to provide evidence on whether mindfulness practices in childbirth preparation classes affect pregnant women's fear of childbirth, prenatal stress, and childbirth self-efficacy.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Pregnant women aged 18 years or older * Gestational age between 28 and 38 weeks * Primiparous (first pregnancy) * Able to understand and speak Turkish * No communication problems that would hinder participation * No high-risk pregnancy as determined by a physician * Able to read and write * Willing to participate in the study and providing informed consent Exclusion Criteria: * • Pregnant women with high-risk pregnancies (history of antepartum bleeding, intrauterine growth restriction, placenta previa, membrane rupture, preeclampsia, hypertension, diabetes, or other medical conditions, fetal anomalies, or any contraindication to normal vaginal delivery, substance or alcohol dependence) * pregnant women with a diagnosed psychiatric illness or who have undergone psychotherapy or medication treatment in the last six months, * pregnant women who have previously participated in childbirth preparation classes, * pregnant women with experience in yoga and meditation before or during pregnancy, * pregnant women with chronic illnesses, * pregnant women who are foreign nationals.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Samsun City Hospital Samsun Turkey (Türkiye)

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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 NCT07415122 on ClinicalTrials.gov ↗ ← All trials in Turkey