Actively Recruiting
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
Eligibility Criteria
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
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
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Trial Site Locations
Total: 1 location
1
Ondokuz Mayis University
Samsun, Turkey (Türkiye), 55200
Actively Recruiting
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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