Drug information presentation Not Applicable
Conditions
Interventions
Randomisation: each time a participant agreed to participate a random number is generated and the participant is allocated to the presentation format according to that number.
The stu
Sponsors
Martin Luther University Halle-Wittenberg
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Adults > 18 years who have their primary residence in Germany and belong to the panel
Exclusion criteria
Exclusion criteria: Does not meet inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Verbatim knowledge/risk perception, which is surveyed by 9 items coded 1 (correct answer) or 0 (incorrect answer), measured immediately after the intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Measured immediately after the intervention: 1. Readability/comprehensibility is measured by four questions using a four-point Likert scale 2. Acceptance is measured by three questions using a four-stage interval scale 3. Relevance refers to the importance of the information. This endpoint is measured with one question | — |
Countries
Germany
Outcome results
None listed