Cross-sector implementation of caregivers for people with dementia

Not Applicable

• Conditions: F00; F01; F02; F03; Dementia in Alzheimer disease; Vascular dementia; Dementia in other diseases classified elsewhere; Unspecified dementia

• Registration Number: DRKS00033281
• Lead Sponsor: Arbeitsgemeinschaft katholischer Krankenhäuser Saarland, Caritasverband für die Diözese Trier e. V.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-12-22
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 600

Inclusion Criteria

Dementia, place of residence in Saarland, benefit recipient according to § 45a/b SGB XI, insured be AOK Rheinland-Pfalz/Saarland or IKK Südwest

Exclusion Criteria

Delirum at hospital admission

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary endpoint is the absence of adverse events during an inpatient stay. This is checked by recording of adverse events in the hospital.

Secondary Outcome Measures

Name	Time	Method
Secondary endpoints are the burden of adverse events during the inpatient stay, as determined by a score, and the costs from the perspective of the statutory health and long-term care insurances in a period of 90 days after discharge. The occurrence of adverse events is recorded in the hospital. The costs are taken from the routine data of the insurances.