RecruitingNot ApplicableNCT06927804

Utilization of Virtual Reality to Increase Comfort and Reduce Procedural Distress During Port Insertion Into the Body

Utilization of Virtual Reality to Support Patient Comfort and Reduce Stress During the Implantation of a Subcutaneous Venous Port Prior to the Initiation of Oncological Treatment


Sponsor

University Hospital Ostrava

Enrollment

60 participants

Start Date

Jul 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This randomised controlled study evaluates whether virtual reality (VR) can support patient comfort and help reduce anxiety and stress during subcutaneous venous port implantation in adult oncology patients. Patients will be assigned to standard care or standard care with VR intervention. Subjective and objective measures of stress and discomfort will be collected, including the Visual Analog Scale (VAS) for self-reported procedural discomfort, physiological parameters (blood pressure, heart rate, variability), the STAI-6 questionnaire, and salivary cortisol. The study aims to explore the potential of VR as a non-pharmacological, immersive tool to improve procedural experience and reduce psychological distress in patients undergo-ing minor oncological procedures.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Patients \> 18 years of age
  • Signed Informed Consent Form
  • Patients Indicated for oncology treatment administration using subcutaneous port

Exclusion Criteria3

  • Not signing of the Informed Consent Form
  • Patients \< 18 years of age
  • Patients unsuitable for subcutaneous port implantation

Interventions

PROCEDUREStandard Care (in control arm)

Patients in this study arm will receive standard care, without the use of VR.

PROCEDUREVirtual reality intervention

A virtual reality device will be used in one study arm during the implantation of the subcutaneous port.


Locations(1)

University Hospital Ostrava

Ostrava, Moravian-Silesian Region, Czechia

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NCT06927804