Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07247643

The Impact of Virtual Reality Glasses on Maternal Satisfaction and Postpartum Comfort in Cesarean Sections Performed Under Spinal Anesthesia

Due to the stressful nature of cesarean birth, it is important that the use of virtual reality (VR) glasses is both feasible and effective. While wearing VR glasses, the distraction effect can reduce women's focus on pain and the surgical procedure itself. Furthermore, VR applications have been shown to increase women's satisfaction with the birth experience. This study will be conducted as a randomized controlled trial. A total of 96 participants will be included, with 48 assigned to the intervention group and 48 to the control group. The intervention group will consist of women undergoing repeat cesarean section under spinal anesthesia. During the procedure, participants in the intervention group will watch nature videos with sound through VR glasses. The VR application will be paused when the baby is born to allow for initial neonatal care and skin-to-skin contact. After skin-to-skin contact has been established, the VR application will resume and continue until the completion of the suturing process. Subsequently, once the women are transferred to the ward, the "Personal Information Form," the "Postpartum Comfort Scale," and the "Cesarean Birth Satisfaction Scale for Women Under Spinal Anesthesia," developed by the researcher, will be administered at an appropriate time. This study is expected to support healthcare professionals in integrating VR technology into childbirth practices by providing insights into women's experiences with this intervention. In this way, the study aims to reduce negative emotions experienced during cesarean birth, support the postpartum recovery process, and enhance overall patient satisfaction. Moreover, the findings will contribute to improving the feasibility of digital innovations in healthcare, enhancing the quality of birth experiences, and strengthening the approach to patient-centered care.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Conditions

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Women aged 18-45 years

Undergoing elective repeat cesarean section under spinal anesthesia

Able to communicate in Turkish and provide informed consent

Singleton pregnancy

Exclusion criteria

Presence of obstetric or medical complications requiring general anesthesia

Emergency cesarean sections

Psychiatric or neurological disorders that may interfere with VR use

Contraindications to spinal anesthesia

Visual or hearing impairments preventing effective use of VR glasses

Treatment and study plan

(Intervention Group): Virtual Reality Glasses

Device

Participants in this group will undergo cesarean section under spinal anesthesia and, during the procedure, will watch immersive nature videos with sound through virtual reality (VR) glasses. The VR application will be paused at the time of birth to allow for initial newborn care and skin-to-skin contact, and then resumed until the completion of suturing. Standard perioperative care will also be provided.

Control Group

Other

Participants in this group will undergo cesarean section under spinal anesthesia and will receive routine perioperative care only, without the use of virtual reality.

Primary outcomes

  1. Cesarean Birth Satisfaction

    Time frame: Within 48 hours after cesarean delivery

    Women's satisfaction with their cesarean delivery experience will be assessed using the researcher-developed "Cesarean Delivery Satisfaction Scale for Women Under Spinal Anesthesia." It will be measured using a researcher-developed 11-item, 5-point Likert-type scale (scores range from 11 to 55), with higher scores indicating greater satisfaction.

Secondary outcomes

  1. Postpartum Comfort

    Time frame: Within 48 hours after cesarean delivery

    Women's postpartum comfort will be measured using the "Postpartum Comfort Scale." It uses a 5-point Likert-type scoring system. The lowest possible score is 34, and the highest is 170. Higher scores indicate greater comfort.

Sponsors and collaborators

Lead sponsor

Büşra Küçüktürkmen

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Nov 25, 2025
Registry last updated
Nov 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.