Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT07016880

Anxiety, Physiological Parameters, Patient Satisfaction and VR in Gynecological Oncology Surgery

Led by Hacettepe University · Updated on 2025-09-10

66

Participants Needed

1

Research Sites

52 weeks

Total Duration

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AI-Summary

What this Trial Is About

Surgical procedures often cause significant anxiety in patients, particularly among women undergoing gynecological oncology surgeries. Preoperative anxiety is a common and preventable condition that can negatively affect both physiological parameters and the overall surgical experience. It may lead to increased heart rate, elevated blood pressure, respiratory distress, and psychological discomfort, increasing the risk of complications during and after surgery. Women facing gynecological cancer surgery often experience heightened anxiety due to concerns about survival, loss of reproductive organs, body image changes, and sexual health. Virtual reality (VR) has emerged as a promising non-pharmacological approach for reducing preoperative anxiety. By immersing patients in a calming virtual environment that engages visual and auditory senses, VR helps promote relaxation, reduce stress, and enhance the patient's sense of control before surgery. It is safe, easy to implement, cost-effective, and does not have the side effects associated with medications. Although VR has demonstrated effectiveness in reducing anxiety in various surgical contexts-including orthopedic, colorectal, and minor gynecological procedures-its impact in gynecologic oncology surgery remains underexplored. This randomized controlled trial aims to evaluate the effect of a VR intervention on preoperative anxiety, physiological parameters (blood pressure, heart rate, respiratory rate, oxygen saturation), and patient satisfaction in women scheduled for gynecologic oncology surgery. Participants will be randomly assigned to either the intervention group (receiving VR) or the control group (receiving standard care). Anxiety and physiological measures will be evaluated before and after the respective intervention in both groups. Patient satisfaction will be assessed once, immediately after the intervention and before surgery. The primary objective is to assess whether VR effectively reduces preoperative anxiety and stabilizes physiological indicators. The secondary objective is to evaluate patient satisfaction with the preoperative experience. This study will contribute to the evidence base for using VR as a nursing-led, non-invasive strategy to enhance surgical care in gynecologic oncology.

CONDITIONS

Official Title

Anxiety, Physiological Parameters, Patient Satisfaction and VR in Gynecological Oncology Surgery

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of gynecological cancer
  • Awareness of gynecological cancer diagnosis
  • At least 18 years of age
  • Provided verbal and written informed consent
  • Able to communicate verbally and in writing in Turkish
  • No communication impairments such as visual, auditory, or cognitive problems
  • Scheduled for first surgical intervention related to gynecological oncology
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 2 or less
  • Planned surgery is a laparotomy
Not Eligible

You will not qualify if you...

  • History of recurrent gynecological cancer
  • Vision problems preventing use of VR goggles, including uncorrected vision impairment or wearing glasses
  • Conditions like migraines, vertigo, active nausea, vomiting, or frequent headaches
  • Sensitivity to motion sickness
  • Psychiatric diagnosis under any treatment
  • Withdrawal of consent during the study
  • Removal of VR headset during intervention
  • Development of medical complications during intervention

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Hacettepe University

Ankara, Turkey (Türkiye), 06100

Actively Recruiting

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Research Team

F

Fatma Uslu Sahan, Assoc Prof

CONTACT

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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