None listed
Conditions
Interventions
Group 1: The control group will receive the prevalent way of informing before a CT-scan, which contains a text and a medical questionnaire printed on paper and the following conversation with a doctor
Sponsors
Universitätsklinikum Ulm, Kliniken am oberen Eselsberg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The participant must be able to give his consent and must be able to write. The participation is voluntary.
Exclusion criteria
Exclusion criteria: Incapacitated persons or persons, who cannot write
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| questionnaire-based, case-control study, which deals with the comparison between the prevalent and a digital, video-based way of informing about the CT-scan. The quesionnaire for patients records satisfaction, understanding of the CT-scan and openness for increasing digitalization. The quesionnaire for informing doctors records satisfaction. | — |
Secondary
| Measure | Time frame |
|---|---|
| time mesuring to record the average time the doctor needs to inform patients in the control grop and in the experimental group. | — |
Countries
Germany
Contacts
Public ContactAndrea Nedelcu
Klinik für Diagnostische und Interventionelle Radiologie Universitätsklinikum Ulm
Outcome results
None listed