no disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Operators who are certified IR/IOs, performing interventional vascular and oncology procedure - Operators that are 18 years of age or older, or of legal age to give informed consent per state or national law. - Procedures taken place in the angiography suite, with the same criteria as for the normal procedures that are not limited to standard angiographic I/O procedures and Image-Guided drainages using ultrasound or fluoroscopy. - Patients elected for the procedures described, that are able to give informed consent per state or national law.
Exclusion criteria
Exclusion criteria: - Operator or subject is Philips employee or their family members residing with this Philips employee. - Operators that wear normal eye wear that do not fit underneath the AR HMD. - Operators that are color blind and or have strabismus as eye deficiencies. - All vulnerable subjects such as subjects lacking the capacity to provide consent, patients in emergency situations, pregnant or breast feeding women, or any other subject who meets an exclusion criteria, according to applicable national laws, if any.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Meaningfulness: The operator will rate the meaningfulness on a 11 point Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Usability: The operator will rate the usability of the Azurion AR. It will be assessed by using the System Usability Score (SUS). - Image quality: The operator will rate the image quality of the virtually presented medical images on a 5 point Likert Scale. - Ergonomics: The operator will indicate to what extend he/she is affected by 17 prompted symptoms using the visual fatigue questionnaire. - Workload: The operator will fill out a task load questionnaire, the raw version of the NASA Task Load Index (TLX) to assess the workload on six subscales with 21 gradations. | — |
Contacts
Philips Medical Systems Nederland B.V.