C61
Conditions
Interventions
Group 1: standard preoperative informed consent procedure
Group 2: additional multimedia support for preoperative informed consent procedure
Sponsors
Urologische Universitätsklinik Heidelberg
Eligibility
Sex/Gender
Male
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Every patient planned to undergo radical prostatectomy at the Department of Urology, Univerity of Heidelberg, as far as he is of full age and able to give informed consent.
Exclusion criteria
Exclusion criteria: Beeing not able or not willing to give informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| patient satisfaction measured in the evening before surgery following the informed consent procedure by standardised interview and self-designed questionnaire (27 items) | — |
Secondary
| Measure | Time frame |
|---|---|
| duration of informed consent procedure measured by stop watch during the informed consent procedure || fear level measured in the evening before surgery following the informed consent procedure by STAI-questionnaire || knowledge measured in the evening before surgery following the informed consent procedure by standardised interview and self-designed questionnaire (27 items) || feeling of security measured in the evening before surgery following the informed consent procedure by standardised interview and self-designed questionnaire (27 items) || confidence measured in the evening before surgery following the informed consent procedure by standardised interview and self-designed questionnaire (27 items) || clearness measured in the evening before surgery following the informed consent procedure by standardised interview and self-designed questionnaire (27 items) || patient's involvement measured in the evening before surgery following the informed consent procedure by COMRADE-questionnaire | — |
Countries
Germany
Contacts
Public ContactDr. phil. Johannes Huber
Urologische Universitätsklinik Heidelberg
Outcome results
None listed