Virtual Reality for Patient Informed Consent in Neurosurgery
Recruiting
N/A
Interventional Study
VR-based Informed Consent
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 75
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 34 (estimated)
- Sponsor
- University Hospital, Basel, Switzerland · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
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
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Contacts