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Clinical Trials in Turkey / NCT07496879
Enrolling by invitation Not applicable

QR-Based Virtual Tour and Childbirth Outcomes

NCT07496879 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-01
Last updated
2026-03-27

Condition(s) studied

Fear of ChildbirthPrimiparous WomenVaginal Birth RateChildbirth Readiness

Investigational drug(s) / intervention(s)

Virtual Delivery Room Tour via QR Codes

Virtual Delivery Room Tour via QR Codes: Three short videos via QR codes on admission, labor room, and postpartum care.

Study summary

Childbirth is a unique experience that affects maternal health physiologically, emotionally, and socially, and represents a crucial step in the transition to motherhood. Primiparous women often experience fear related to childbirth due to uncertainty about the process, pain, or possible complications. This randomized controlled trial aims to evaluate the effect of a QR code-based virtual tour of the delivery room on primiparous women's fear of childbirth, childbirth readiness, vaginal birth rate, and postpartum breastfeeding self-efficacy. Participants will be provided access to three virtual videos via QR codes, allowing them to explore the delivery room, understand the admission process, and learn about postpartum care. The study will assess outcomes using validated scales for childbirth fear, prenatal readiness, birth-related self-efficacy, and postpartum breastfeeding. By familiarizing participants with the delivery environment, this intervention aims to reduce fear, improve confidence and preparedness, and encourage vaginal delivery. The findings are expected to inform strategies to enhance maternal experiences, support national initiatives such as the Normal Birth Action Plan, and contribute to safer, more satisfying birth and breastfeeding outcomes.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Being literate * Being 18 years of age or older * Being primigravida * Being between 28-32 weeks of gestation * Owning a smartphone * Having internet access * Being able to speak and understand Turkish Exclusion Criteria: * Multiparity * High-risk pregnancy * Having a diagnosed psychiatric disorder Failure to complete the questionnaires during the study period Preterm birth or pregnancy loss before completion of the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Atatürk University - Faculty of Health Sciences, Department of Midwifery Erzurum Yakutiye

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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 NCT07496879 on ClinicalTrials.gov ↗ ← All trials in Turkey