F05.0 F05.1
Conditions
Interventions
Group 1: Pre-intervention group (control group) = measurement of prevalence and incidence of delirium (without Intervention)
Group 2: Intervention group = Measurement of the effect of a systematic, da
Sponsors
UMM MannheimMedizinische Klinik IISektion Altersmedizin/Geriatrisches Zentrum
Eligibility
Sex/Gender
All
Age
65 Years to 105 Years
Inclusion criteria
Inclusion criteria: Patients aged 65 and over (with and without cognitive impairments/dementia); patients with and without delirium at admission, non-ethyltoxic genesis; acute geriatric treatment.
Exclusion criteria
Exclusion criteria: Patients with severely impaired communication skills; estimated hospital stay less than 48 hours.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Collection of primary endpoints of delirium-incidence and prevalence by secondary analysis of routine clinical data of each included patient treated in acute-geriatric ward in the pre-intervention phase (01.10.2018-28.02.2019) and in the intervention phase (01.06.2019-31.10.2019). | — |
Primary
| Measure | Time frame |
|---|---|
| Aim: Further development of interprofessional teamwork. T0= before the intervention phase (03(2019); T1= after the intervention phase 11/2019 using the Assessment of Interprofessional Team Collaboration Scale (AITCS-II). | — |
Countries
Germany
Contacts
Public ContactClaudia Eckstein
Universitätsmedizin Mannheim, II Medizinische Universitätsklinik, Sektion Altersmedizin,
Outcome results
None listed