any somatic condition for which VR is part of CAU to reduce pain or anxiety
Conditions
Interventions
Questionnaire for evaluating the user satisfaction and usability in virtual rehabilitation systems  
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
2 Years to 64 Years
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in the first phase of the current study, a subject must meet all of the following criteria: Age 6-18 at inclusionReceiving either outpatient or inpatient medical care at the hospital for any somatic conditionIndication of VR intervention as part of care as usual to reduce pain or anxietyInformed consent from patient and/or parents or legal representatives (depending on the age)
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in the first phase of the current study: Developmental delayAdmitted to the Intensive Care Unit (ICU) because of mechanical ventilation or sedation History of epilepsySevere visual impairmentHead wounds Not a native Dutch-speakerDeemed not fit to participate due to any reason (e.g. high anxiety or too much pain)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary objective: Primary outcome measure is a Dutch-translated version of the original English USEQ, adapted for use in a Dutch-speaking pediatric population. The USEQ is an English validated measurement for assessing usability and user satisfaction in virtual rehabilitation systems. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary objectives: What are the psychometric properties of a Dutch translation of the USEQ for measuring user satisfaction and usability in a Dutch-speaking pediatric population? | — |
Countries
Netherlands
Contacts
Public ContactS.E. Hoeks
Erasmus MC, Universitair Medisch Centrum Rotterdam
Outcome results
None listed