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Clinical Trials in Turkey / NCT07518667
Starting soon Not applicable

Binaural Beat Music, Virtual Reality, and Hormones in Childbirth

NCT07518667 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-05
Last updated
2026-04-08

Condition(s) studied

BirthHormonesVirtual RealityMusic

Investigational drug(s) / intervention(s)

Virtual reality experienceBinaural Beats-Supported Music Group

Virtual reality experience: Meta Quest 3 virtual reality glasses will be used in the study. Video content was selected from literature. Participants will be shown a virtual reality video created from nature, lake, and ocean floor images. The video content will be pre-loaded onto the device's internal memory, enabling practical use in the delivery room without requiring an internet connection.

Binaural Beats-Supported Music Group: The Acemaşiran maqam was chosen for the binaural beats-supported music group, in accordance with the relevant literature. The music will be provided using binaural beats sound.

Study summary

This study aims to investigate the effects of Binaural Beats-supported music and virtual reality experience on the levels of oxytocin, prolactin, catecholamine, endorphin, prostaglandin E and cortisol, which are hormones that play an active role in birth, using the Elisa method. Additionally, the study will examine the effects of virtual reality experience and Binaural Beats-supported music during labor on labor pain and some birth outcomes (such as the presence of an episiotomy, the onset of labor, the duration of labor, and the newborn Apgar score).The randomized controlled study will consist of three groups: a virtual reality group, a Binaural Beats-supported music group, and a control group. The research will be completed with a total of 90 people, with 30 people in each group. The research will be conducted at the Maternity Ward of Istanbul Gaziosmanpaşa Training and Research Hospital. Ethics committee approval has been received for the research. Data collection has not yet begun. An application has been made to the hospital administration for institutional permission. The research will begin once the permissions are received.

Eligibility

Sex
FEMALE
Min age
20 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Able to speak Turkish and communicate verbally * No hearing or visual impairments * The pregnancy is at term (37-42 weeks of gestation) and labor has begun * Single fetus with cephalic presentation * No chronic disease * Not taking hormone therapy * Pregnant women who do not have any obstetric risks and are expected to give birth normally Exclusion Criteria: * Diagnosed with risky pregnancy * Complications during birth * Those with vision and hearing problems * Any pharmacological pain-reducing method applied * Cesarean section planned * Those who have experienced any alternative methods for preparing for birth or managing labor pain (such as yoga, meditation, breathing exercises, hypnosis)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul Medipol University Beykoz Istanbul

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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 NCT07518667 on ClinicalTrials.gov ↗ ← All trials in Turkey