|
Main
|
|
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
|
Register:
|
German Clinical Trials Register |
|
Last refreshed on:
|
8 April 2024 |
|
Main ID: |
DRKS00010654 |
|
Date of registration:
|
21/06/2016 |
|
Prospective Registration:
|
Yes |
|
Primary sponsor: |
|
|
Public title:
|
Patient satisfaction in the Emergency Department
|
|
Scientific title:
|
Patient satisfaction in the Emergency Department - HappiER |
|
Date of first enrolment:
|
01/07/2016 |
|
Target sample size:
|
3000 |
|
Recruitment status: |
Complete |
|
URL:
|
http://drks.de/search/en/trial/DRKS00010654 |
|
Study type:
|
observational |
|
Study design:
|
Allocation: ; Masking: ; Control: ; Assignment: ; Study design purpose: health services research
|
|
Phase:
|
|
|
|
Countries of recruitment
|
|
Germany
| | | | | | | |
|
Contacts
|
|
Name:
|
Martin
Kulla |
|
Address:
|
Oberer Eselsberg 40
89081
Ulm
Germany |
|
Telephone:
|
0049 151 65613966 |
|
Email:
|
martin.kulla@uni-ulm.de |
|
Affiliation:
|
Bundeswehrkrankenhaus UlmKlinik für Anästhesiologie, Intensivmedizin, Notfallmedizin und Schmerztherapie |
|
|
Name:
|
Martin
Kulla |
|
Address:
|
Oberer Eselsberg 40
89081
Ulm
Germany |
|
Telephone:
|
0049 151 65613966 |
|
Email:
|
martin.kulla@uni-ulm.de |
|
Affiliation:
|
Bundeswehrkrankenhaus UlmKlinik für Anästhesiologie, Intensivmedizin, Notfallmedizin und Schmerztherapie |
| |
|
Key inclusion & exclusion criteria
|
Inclusion criteria: INCLUSION CRITERIA (AND)
- Until April 2017: ambulant patient of the emergency department of the Bundeswehr Hospital Ulm, Germany
- Since April 2017: all atient of the emergency department of the Bundeswehr Hospital Ulm, Germany
- verbal agreement of all employees of the emergency department in the corresponding shift
- patient age > 15 years
- patient must understand the content and the propose of the study
- patient must be able to agree to the study
- written consent of the patient that he / she agrees to the study
Exclusion criteria: EXCLUSION CRITERIA (OR)
- refusal of the patient
- refusal of the employee of the emergency department
- patient is part of an other clinical trail
- cognitive deficits of the patient / patient is not able to understand the content of the study
- patient does not understand the Germany langue
- Until April 2017: patient is admitted to the hospital
Age minimum:
16 Years
Age maximum:
120 Years
Gender:
All
|
|
Health Condition(s) or Problem(s) studied
|
|
all not-admitted patients of an Emergency-Department
|
|
Intervention(s)
|
|
Group 1: After finishing their treatment, all patients of an Emergency Department are asked if they whant to be part of the study. If they agree, an independent investigator determins the patients satisfaction unsing a standardized questionary. Until April 2017 only ambulant (non-admitted) patients have been included. Since April 2017 all patients are included.
|
|
Primary Outcome(s)
|
|
Determination of patient satisfaction. An investigator uses a standardized questionary after the treatment in the ED is finished. The questionary contains of likert type questions as well as willingness to pay questions.
|
|
Secondary Outcome(s)
|
|
development of a prognostic model (score) to determine if a patient will be unhappy with the treatment in the ED
|
|
Source(s) of Monetary Support
|
|
Bundeswehrkrankenhaus UlmKlinik für Anästhesie und IntensivmedizinSektion Notfallmedizin
|
|
Bundesministerium für Verteidigung Sanitätsakademie der Bundeswehr Wehrmedizinische Sonderforschung Abteilung EProjekt ID: SoFo: 37K3-S-20 1618
|
|
Ethics review
|
Status: Approved
Approval date: 02/06/2016
Contact:
ethik-kommission@uni-ulm.de
Ethikkommission der Universität Ulm
+49-731-50022050
ethik-kommission@uni-ulm.de
|
|