Indication various
Conditions
Interventions
Group 1: Questionnaire for clinicians and patients
Sponsors
Studienzentrum des Universitätsklinikums Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Clinicians: - Persons who obtain informed consent - Written informed consent Patients: - Age = 18 years - Persons after a informed consent for an actual clinical trial - Persons with legal capacity who is able to understand the nature, significance and consequences of the communication study - Written informed consent
Exclusion criteria
Exclusion criteria: Clinicians: - Persons who are in a relationship of dependence with the investigator - Persons who had already participated in this study Patients: - Persons where a power-of-attorney for health care is to be given - Known or persistent abuse of medication, drugs or alcohol - Persons who are in a relationship of dependence with the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| How easy can clinicians appraise their patients regarding their reasons for or against participating in an actual clinical trial? Data will be collect by a questionnaire. This questionnaire has to be filled in by clinicians and patients after informed consent. | — |
Secondary
| Measure | Time frame |
|---|---|
| Is the concordance between reasons, patients have for or against participating in a clinical trial and reasons clinicians assume they have depending on - how well the clinicians know the patients? - the time clinicians are on duty? - number of attending communication skills courses? Data will collect by a questionnaire which clinicians have to fill in after informed consent. | — |
Countries
Germany
Contacts
Public ContactBirgit Grotejohann
Studienzentrum des Universitätsklinikums Freiburg
Outcome results
None listed