Clinical Trial

Evaluating the Effectiveness of Virtual Reality Application in Caesarean Section

Active, Not Recruiting
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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?
Trial Details
NCT Number NCT07080281
Lead Sponsor Ankara Yildirim Beyazıt University
Conditions Virtual Reality Pain Distraction, Birth Satisfaction, Vital Signs, Anxiety, Apgar Score, Virtual Reality
Enrollment 55 participants
Start Date 2024-11-15
Primary Completion 2025-06-01 (estimated)
Study Completion 2025-07-15 (estimated)
Updated on ClinicalTrials.gov 2025-07-23