Using virtual reality to improve aneurysm surgeries and patient communication

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study evaluates the impact of virtual reality (VR) on aneurysm surgeries by focusing on two main areas: VR-assisted clip planning and VR-assisted patient-informed consent. The study aims to assess how VR can enhance clinical outcomes, improve patient safety, and reduce surgery times, while also examining its effects on patient comprehension, anxiety, and the patient-doctor relationship. By leveraging VR technology, the research seeks to promote shared decision-making and patient-centered care in neurosurgery. The feasibility and cost-benefit ratio of these VR applications will also be analyzed.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* The patient is able to give written consent (or written consent by legal representative)
* Preoperative imaging demonstrating intracranial pathology
* Cognitively able to provide answers for the questionnaires

Exclusion Criteria:

* No informed consent
* Adult patients without the power of judgement

Where it's running

• University Hospital Basel
  Basel, Switzerland Recruiting

Study contacts

• Principal investigator: Attill Saemann, MD — University Hospital, Basel, Switzerland
• Study coordinator: Attill Saemann, MD
• Email: neurochirurgie@usb.ch
• Phone: +41 61 265 71 24

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.