This study does not investigate diseases. It is about patients who visit the emergency room due to various complaints.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Triage category 3–5 and MTS-indicator „Unwell Adult“ - Patient has not yet been in contact with the treating physician for his or her ED visit
Exclusion criteria
Exclusion criteria: - Incapable of giving consent (e.g., due to acute cognitive impairment, disturbance of consciousness, intoxication) - Medical transport or admission by emergency services or doctor's office - Insufficient German language skills for information and consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of the study is the patients’ subjective experience associated with the use of the digital demonstrator during waiting time in the emergency department. Specifically, the following aspects are assessed: Self-reflection on one’s own health status (based on TSRI), and perceived patient empowerment during waiting time (PEN-13). Data collection takes place during the quantitative evaluation phase (study phase 3). | — |
Secondary
| Measure | Time frame |
|---|---|
| - Subjective preparation for the medical consultation, assessed using open-ended questions inspired by patient-reported outcome measures (e.g. PROM-ED) - Understanding of emergency department processes, captured through structured open-ended questions - User acceptance and evaluation of the demonstrator, defined as the proportion of patients rating the tool as comprehensible, helpful, and meaningful (using UEQ-10, AttractDiff) - Assessment of information quality and potential clinical usefulness of the structured patient inputs from the perspective of physicians and nursing staff (qualitative evaluation in study phase 4) | — |
Countries
Germany
Contacts
Charité – Universitätsmedizin Berlin Notaufnahmen Campus Mitte und Campus Virchow Klinikum, Notfallmedizinische Versorgungsforschung