Functional decline, immobility, falls, delirium and rehospitalization
Conditions
Interventions
Group 1: Intervention group:
-risk screening
-individualized intervention consisting of up to six modules. (1) individualized health information, (2) delirium prevention, (3) mobility training, (4) c
Sponsors
Universitätsklinikum Freiburg
Eligibility
Sex/Gender
All
Age
70 Years to No maximum
Inclusion criteria
Inclusion criteria: acute inpatients = 70 years of age, increased risk for functional decline, immobility, falls, delirium, or rehospitalisation, informed consent
Exclusion criteria
Exclusion criteria: Patients receiving palliative care in the final phase.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurement time points: t0 (baseline), t1 (hospital discharge), t2 (after 6 months): (1) Mobility Mobilität (Short Physical Performance Battery (SPPB)) (2) activities of daily living (Barthel scale) | — |
Secondary
| Measure | Time frame |
|---|---|
| Measurement time points: t0 (baseline), t1 (hospital discharge), t2 (after 6 months): (3) falls (frequency and injuries/fractures) (4) Delir (3D-CAM) (5) cognition (Montreal Cognitive Assessment (MOCA)) (6) health-related quality of life (SF-12) (7) hand strength (dynamometer) (8) potentially inadequate medication (PIM) (STOPP/START) Measurement time point: t3 (two subsequent quarters after discharge): (9) Health economic evaluation of AOK routine data/ rehospitalisation | — |
Countries
Germany
Contacts
Public ContactFelix Kentischer
Universitätsklinikum Freiburg
Outcome results
None listed