Evaluation after informed consent
- Conditions
- Indication various
- Registration Number
- DRKS00000743
- Lead Sponsor
- Studienzentrum des Universitätsklinikums Freiburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 41
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
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
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method How easy can clinicians appraise their patients regarding their reasons for or against participating in an actual clinical trial?<br>Data will be collect by a questionnaire. This questionnaire has to be filled in by clinicians and patients after informed consent.
- Secondary Outcome Measures
Name Time Method Is the concordance between reasons, patients have for or against participating in a clinical trial and reasons clinicians assume they have depending on<br>-how well the clinicians know the patients?<br>-the time clinicians are on duty?<br>-number of attending communication skills courses?<br><br>Data will collect by a questionnaire which clinicians have to fill in after informed consent.