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Clinical Trials in Turkey / NCT07080281
Active, not recruiting Not applicable

Evaluating the Effectiveness of Virtual Reality Application in Caesarean Section

NCT07080281 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-11-15
Last updated
2025-07-23

Condition(s) studied

Virtual Reality Pain DistractionBirth SatisfactionVital SignsAnxietyApgar ScoreVirtual Reality

Investigational drug(s) / intervention(s)

Oculus Meta Quest 2 All In-One model virtual reality glasses

Oculus Meta Quest 2 All In-One model virtual reality glasses: During the caesarean section, Meta Quest 2 All In-One model virtual reality glasses from Oculus were used for 15 minutes. In this virtual environment, the licensed product video "Breathe- Relax and Meditate" was watched via the "Meta Horizon" application.

Study summary

The aim of this study was to evaluate the effects of virtual reality intervention during cesarean delivery under spinal anesthesia on labor pain, anxiety, satisfaction and hemodynamic parameters in primiparous pregnant women.

The main questions it aims to answer are:

1. Is there a significant difference between the mean intraoperative pain scores of the pregnant women in the intervention group and those in the control group?
2. Is there a significant difference between the mean intraoperative anxiety scores of the pregnant women in the intervention group and those in the control group?
3. Is there a significant difference between the mean birth satisfaction scores of the pregnant women in the intervention group and those in the control group?
4. Is there a significant difference between the vital signs of pregnant women in the intervention group and those in the control group?
5. Is there a significant difference between the mean apgar scores of the pregnant women in the intervention group and those in the control group?

Eligibility

Sex
FEMALE
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 19 years of age and older, * Turkish speaking, * At least primary school graduate, * Between 37th and 42nd weeks of pregnancy, primiparous and with a single fetus, * No diagnosed psychiatric problem (anxiety disorder, bipolar disorder, schizophrenia, etc.), * No epilepsy diagnosis, * No hearing, vision or communication impairment, * Spinal anesthesia planned, * Pregnant women who volunteered to participate in the study were included. Exclusion Criteria: * Incomplete data collection forms, * Participant's refusal to participate in the study at any stage, * Use of general anesthesia/sedation during the cesarean section process, * Only for pregnant women in the intervention group; not fully participating in the virtual reality glasses training, not using the virtual reality glasses for the desired duration, or having side effects of the virtual reality glasses (dizziness, headache, sweating, nausea, vomiting or eye strain) are the exclusion criteria from the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Yildirim Beyazit University, Faculty Of Health Sciences Ankara Çubuk

More Ankara Yildirim Beyazıt University trials in Turkey

Other trials for the same condition

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 NCT07080281 on ClinicalTrials.gov ↗ ← All trials in Turkey