The inclusion criteria for patients with a corresponding general medical disease spectrum in STATAMED are described in another sub-study (see DRKS00033096).
Conditions
Interventions
Group 1: In the course of implementing the intervention, the SOPs are reviewed twice during the project using scientific quality circles and then revised. Only during implementation will it become cle
all locations have at least 3 months of intervention behind them)
2. Revision/addition and roll-out of the revised SOPs: 12 months after the first transition phase (all locations have at least 6 month
5-10 participants per group). The following groups are planned:
• 2 groups each of STATAMED doctors
• 2 groups each of patient guides and flying nurses
• 4 groups of medical referrals
•
Sponsors
AOK Rheinland/Hamburg - Die Gesundheitskasse
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: In principle, people of all genders (male/female/male) and any ethnic background who are at least 18 years old can take part in the study. Participants belong to the following target groups within the framework of the qualitative sub-study: service providers in STATAMED facilities and providers at the respective evaluation sites, e.g. medical and nursing staff in STATAMED, patient guides, flying nurses, medical referrals, emergency services, nursing facilities, outpatient nursing services; employees of the affiliated ZNAs. After receiving comprehensive oral and written information about the nature, content and purpose of the study, the participants sign a written consent to participate in the study.
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoints of the evaluation of the main study (e.g. re-hospitalizations and length of inpatient stay) are being investigated by another cooperation partner (DRKS00033096) and are not part of this registered sub-study. Aim of the sub-study: The results of the data collection in this sub-study will be used to make a final revision of the SOPs and training materials. This means that at the end of the intervention, materials will be available that will enable the implementation of the STATAMED intervention at other locations. | — |
Secondary
| Measure | Time frame |
|---|---|
| The qualitative sub-study aims to provide insights into the following secondary endpoints: • Understanding and practical implementation of the STATAMED SOPs • Contents and structure of the SOPs | — |
Countries
Germany
Outcome results
None listed