Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
FEMALE
Healthy Volunteers
ID06680141

The Effect of Virtual Reality Glasses Used Before Cesarean Section on Surgical Fear and Anxiety

Led by Ondokuz Mayıs University · Updated on 2025-01-22

120

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate how using virtual reality glasses before a cesarean section affects surgical fear and anxiety in women. The study compares two groups: one that uses virtual reality glasses and a control group to understand if the glasses influence anxiety and fear related to surgery. It focuses on women scheduled for their first cesarean section, without prior mental or physical illnesses, to see if this method helps reduce pre-surgery stress. Participants are divided randomly into two groups using block randomization. The virtual reality group wears glasses before surgery and watches a 30-minute video showing fetal development over nine months. The control group does not receive this intervention. Both groups have their surgical fear and anxiety levels recorded before and after the cesarean section using specific scales. During the study, women will complete questionnaires on their background and anxiety using the Surgical Fear Scale and the Spielberger State Anxiety Scale. Researchers will measure fear and anxiety levels 30 minutes before surgery and again after the cesarean section. By monitoring these changes, the study aims to assess whether virtual reality glasses can help lower surgical fear and anxiety. Participation involves informed consent and adherence to study procedures around the time of surgery.

CONDITIONS

Official Title

The Effect of Virtual Reality Glasses Used Before Cesarean Section

Who Can Participate

Age: 18Years - 60Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Will undergo a cesarean section for the first time
  • Are over the age of 18
  • Have no diagnosed mental illness
  • Have no diagnosed physical illness in themselves or their baby
  • Volunteer to participate in the study
Not Eligible

You will not qualify if you...

  • Have previously undergone a cesarean section
  • Are under the age of 18
  • Have a diagnosed mental illness
  • Have a diagnosed physical illness in themselves or their baby
  • Do not volunteer to participate in the study

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Ondokuz Mayis University

Samsun, Turkey (Türkiye), 55200

Actively Recruiting

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Research Team

S

Sümeyye BAL, Ph.D

S

Sümeyye BAL, Ph.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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