The Effect of Virtual Reality Glasses Used Before Cesarean Section

Ondokuz Mayıs University

Status: Enrolling

Conditions: Anxiety

Treatments: Other: Virtual reality glasses

Study type: Interventional

Funder types: Other

Identifiers

NCT06680141

2022/260

Details and patient eligibility

About

The aim of this study is to determine the effect of Virtual Reality Glasses Used Before Cesarean Section on Surgical Fear and Anxiety

Full description

Hypotheses 01; there was no difference between the Surgical Fear and Anxiety score of the Virtual Reality Glasses group and the control group.

The study will be carried out in two different groups. The practice will start with meeting the women whom will go to cesarean section in the hospital. After the women are evaluated in terms of eligibility criteria for the research, the women who are eligible will be informed about the research and written informed consent will be obtained from the women who accept. The random distribution of women to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups.

Virtual Reality Glasses Group; the intervention will be given glasses before the surgery and will be shown a video (30 minutes) of the 9-month fetal development process. Among the women who were admitted for a planned caesarean section, those who met the criteria would first be given the Informed Consent Form and a data collection form including sociodemographic characteristics, surgical fear scale, Spielberg State-Trait Anxiety Scale, and then randomization would be applied.

control group; the first surgical fear scale, anxiety scores will be recorded. After cesarean section anxiety scores will be recorded.

Enrollment: 120 estimated patients

Sex: Female

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 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

Exclusion criteria

• 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. -

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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120 participants in 2 patient groups

Virtual Reality Glasses

Experimental group

Description:

Among the women who have been admitted for a planned caesarean section, the Informed Consent Form and the Data Collection Form including Sociodemographic Characteristics, Surgical Fear Scale, Spielberg State-Trait Anxiety Scale will be applied to the women who meet the criteria and randomization will be applied. After randomization, they will be divided into a virtual reality glasses application group and a control group. All women will be applied the Spielberg State-Trait Anxiety Scale and Surgical Fear Scale in the patient room before and after the SGG application. The experimental group will be shown a video (30 minutes) of the 9-month fetal development process, with glasses on before going to surgery.

Treatment:

Other: Virtual reality glasses

control

No Intervention group

Description:

Participants in the control group received standard care (verbal information about procedure and a short written information about the procedure) and no intervention will perform