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Virtual Reality for Patient Informed Consent in Neurosurgery

Virtual Reality for Patient Informed Consent in Neurosurgery

Recruiting
18-75 years
All
Phase N/A

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Overview

The goal of this randomized controlled trial is to evaluate benefits of VR (virtual reality)-based patient informed consent in neurosurgery regarding subjective patient comprehension, patient-doctor relationship and anxiety.

Description

Additionally, the investigators aim to assess the cost-benefit radio as well as feasibility in a clinical routine setting. Considering the increasing patient participation in decision-making, VR could lead to better understanding of complex surgical procedures, improving the perioperative process for both, patient and surgeon, and reduce anxiety.

Eligibility

Inclusion Criteria:

  • Patients between the age of 18 and 75
  • Surgical clipping for intracranial aneurysm, resection of vascular malformations
  • Craniotomy and Resection of intracranial tumors that can be segmented for VR

Exclusion Criteria:

  • Visual or auditory impairment with no sufficient aid
  • Patient that had VR informed consent for surgery before
  • Psychiatric illness, cognitive impairment

Study details
    VR-based Informed Consent

NCT06627426

University Hospital, Basel, Switzerland

27 August 2025

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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