C00-C97
Conditions
Interventions
Group 1: Patients presented to the MTB also receive a patient protocol from the attending physician that is understandable to laypersons. It is aimed directly at the individual patient and explains th
Sponsors
Universitätsklinikum Essen, Westdeutsches Tumorzentrum
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: -The patient has a defined oncological disease/unique access diagnosis and is assigned to the MTB of the WTZ Essen -Documented patient consent to the MII Broad Consent -Sufficient ability to understand the written information
Exclusion criteria
Exclusion criteria: - incapacity to give consent - lack of declaration of consent in the MII Broad Consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim of the study is to gain insights into the following points (questionnaires for patients) and evaluation of feedbacks by patients: - Need, acceptance and reception (by patients themselves and by their social environment) - Comprehensibility and clarity, - Appreciation and attention, - Scope, type and depth of information and - Empowerment / self-efficacy In addition, the treating physicians are asked about their experiences with MyCODE using a questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcome | — |
Countries
Germany
Contacts
Public ContactIna Pretzell
Universitätsklinikum Essen, Westdeutsches Tumorzentrum
Outcome results
None listed