Endpoit is binary outcome (approval/denial) to broad consent
Conditions
Interventions
Group 1: broad consent patient sample randomly selected by continuosly assigned number in order of attendance to the ED .
Patients will be consented to participate in the study verbally and then are i
Sponsors
Universitäts-Notfallzentrum
Eligibility
Sex/Gender
All
Age
18 Years to 120 Years
Inclusion criteria
Inclusion criteria: All adult emergency patients
Exclusion criteria
Exclusion criteria: Minors
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Informed broad consent success rate within the sample population in emergency patients. Stratified by the urgency, diagnosis, age, gender and the mode of consenting (direct, delayed, authorized person) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Ressources needed for obaining consent (staff, time) - Patient-reported reasons for consenting or declining the consent (nominal category) - staff-reported suspected reasons for consenting or declining the consent (nominal category) - Time to Contact (Arrival to contact with consenting office) - Time to Consent (Arrival to consent or decline) | — |
Countries
Germany
Contacts
Public ContactFelix Hans
Universitäts-Notfallzentrum
Outcome results
None listed