Utilization of Virtual Reality to Increase Comfort and Reduce Procedural Distress During P
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 measu
| Condition(s) | Oncology Patients |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| 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. |
| Who can participate | Inclusion Criteria: * Patients \> 18 years of age * Signed Informed Consent Form * Patients Indicated for oncology treatment administration using subcutaneous port Exclusion Criteria: * Not signing of the Informed Consent Form * Patients \< 18 years of age * Patients unsuitable for subcutaneous port implantation |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | University Hospital Ostrava |
| Locations | Ostrava, Moravian-Silesian Region, Czechia |
| Start date | 2025-07-01 |
| NCT ID | NCT06927804 |
| Official listing | https://clinicaltrials.gov/study/NCT06927804 |