Effect of Virtual Reality on Pain and Anxiety During Pap Smear Testing

Официальное название

The Effect of Virtual Reality Transition on Pain and Anxiety Experienced During Pap Smear Testing

Обзор

This randomized controlled pretest-posttest experimental study aims to evaluate the effect of virtual reality (VR) on pain and anxiety levels experienced during Pap smear sampling. Although cervical cancer is largely preventable through regular screening, many women avoid Pap smear testing due to anxiety, fear of pain, and discomfort during gynecological examinations. Innovative, non-invasive interventions are needed to improve women's screening experiences and participation rates. The study will be conducted in a gynecology outpatient clinic with 60 women aged 18-65 years who meet the inclusion criteria and provide informed consent. Participants will be randomly assigned to either the intervention group (VR headset during the procedure) or the control group (standard care). Women in the intervention group will watch a 360° relaxing nature video during the Pap smear procedure. Data will be collected using a Personal Information Form, the State Anxiety Inventory, and the Visual Analog Scale (VAS). The findings may support integrating VR into clinical practice to enhance patient comfort during screening procedures.

Подробное описание

This study was planned as a randomized controlled, pretest-posttest true experimental design to evaluate the effect of a virtual reality (VR) application on pain and anxiety levels experienced by women during Pap smear sampling. Although cervical cancer is preventable, it remains a significant cause of morbidity and mortality among women worldwide. Despite the availability of regular screening programs, many women are reluctant to undergo Pap smear testing due to factors such as pain, anxiety, and concerns about privacy during gynecological examinations. Therefore, there is a need for innovative and non-invasive methods to reduce negative experiences during the procedure.

The study will be conducted at the Gynecology and Obstetrics Outpatient Clinic of Gazimağusa Yaşam Hospital. The sample will consist of 60 women aged 18-65 years who meet the inclusion criteria and voluntarily agree to participate. Participants will be randomly assigned to either the intervention group (VR headset applied) or the control group (standard care) using a simple randomization method.

Women in the intervention group will watch a 360° relaxing nature video through a virtual reality headset during the Pap smear procedure. The control group will receive the standard clinical procedure. Data will be collected using a Personal Information Form, the State Anxiety Inventory, and the Visual Analog Scale (VAS). Anxiety levels will be assessed before and after the procedure, and pain levels will be evaluated after the procedure.

The findings are expected to demonstrate the effectiveness of virtual reality in reducing pain and anxiety during Pap smear procedures and to contribute to evidence-based practices aimed at increasing women's participation in cervical cancer screening programs.

Вмешательства

• Поведенческое Virtual Reality
  Participants will watch a 360° relaxing nature video through a VR headset during the Pap smear procedure.

Первичные конечные точки

• Pain level during Pap smear procedure [Срок оценки: Immediately after completion of the Pap smear procedure (within 5 minutes post-procedure).]
• State anxiety level [Срок оценки: Immediately before the procedure and immediately after the procedure.]

Критерии участия

Критерии включения

• Women aged 18-65 years
• Scheduled for a Pap smear procedure
• Able to communicate in Turkish
• Able to understand and complete the study questionnaires
• Willing to provide written informed consent
• No visual or hearing impairment preventing the use of a VR headset

Критерии исключения

• History of severe motion sickness or vertigo
• Diagnosed psychiatric disorder affecting anxiety assessment
• Use of anxiolytic or sedative medication within 24 hours prior to the procedure
• Presence of acute pelvic pain or active vaginal infection
• Previous participation in this study
• Any condition preventing safe use of a VR headset

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Простое слепое

Основная цель

Поддерживающая терапия

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07462039 · ETK-00-2025-0190

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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