Virtual Reality for Patient Informed Consent in Neurosurgery

Recruiting now · Not applicable

Conditions studied: VR-based Informed Consent

In brief

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.

Key facts

Study ID

NCT06627426

Run by

University Hospital, Basel, Switzerland

People needed

34

Starts

2024-10-22

Expected to finish

2025-10-15

Last updated by the study team

2025-02-11

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

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

Where it is running

• University Hospital Basel — Basel, Switzerland (enrolling)

Full record on ClinicalTrials.gov

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