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AdvantAGE: Implementation and Evaluation of an Interprofessional Tranistional Care Model for Frail Older Adults

AdvantAGE: Implementation and Evaluation of an Interprofessional Transitional Care Model for Frail Older Adults at the University Department of Geriatric Medicine FELIX PLATTER

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06190288
Acronym
AdvantAGE
Enrollment
250
Registered
2024-01-05
Start date
2024-01-08
Completion date
2026-06-30
Last updated
2024-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Geriatric Care, Multimorbidity, Transitional Care

Keywords

Transitional Care, Frailty, Rehospitalisation, Geratric Care

Brief summary

This clinical trial at the University Department of Geriatric Medicine FELIX Platter in Basel, Switzerland, is designed to evaluate a new transitional care model aimed at helping frail older adults after they get discharged from the hospital. The AdvantAGE study aims to explore the following questions: * Does the new care model help reduce the number of patients who need to return to the hospital within 90 days? * How effective is the implementation of this care model? Participants in the trial will be followed by advanced practice nurses for up to 90 days after hospital discharge. The patients and their caregivers will receive support in coordinating care, managing medications, and learning to manage the patient's health conditions on their own. Additionally, they will have the opportunity to engage in discussions about advanced care planning.

Interventions

A newly developed care model to support frail older adults during their transition from hospital to home.

Sponsors

Health Department of the Canton of Basel-Stadt
CollaboratorOTHER_GOV
Thekla Brunkert
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Hybrid effectiveness-implementation study (type 1)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Currently admitted to the acute or rehabilitation ward of University Department of Geriatric Medicine * Reside in Basel-Stadt * Possess the ability to speak and comprehend the German language * Scheduled to be discharged to their home * 65 years or older * Identified by a clinician as having a high risk of deterioration due to frailty Additionally, participants must meet at least one of the following criteria: * diagnosed with a complex chronic disease requiring support in self-management and disease management, or * facing socially challenging situations such as living alone without a supportive network or lacking a GP, or * admitted for an acute illness with a brief hospital stay (e.g., infection, cardiac decompensation) and need support in self- and disease management, and continuity of the therapy plan, including close monitoring.

Exclusion criteria

* residing in a nursing home or being newly admitted to one * lacking informal caregivers and exhibiting severe cognitive impairment (MMS ≤23) * scoring \<50 on the motoric domain of the Functional Independence Measure (FIM) * having a psychiatric disorder that significantly impacts their ability to manage daily life at time of the discharge

Design outcomes

Primary

MeasureTime frameDescription
90-days rehospitalization rate90 days post-dischargeNumber of unplanned hospital admissions of any kind happening within 90 days after discharge

Secondary

MeasureTime frameDescription
Time to readmissionUp to 90 days post-dischargeNumber of days between hospital discharge and unplanned hospital admission
Number of emergency room visits90 days post-dischargeNumber of emergency room visits (with or without hospital admission) within 90 days after discharge
30-days rehospitalization rate30 days post-dischargeNumber of unplanned hospital admission of any kind happening within 30 days after discharge
Patient's health-related quality of lifeUp to 90 days post-dischargeThe EuroQoL-5D-5L is used to assess the health-related quality of life in patients at three time points. Prior to hospital discharge, 7 days and 90 days after hospital discharge or if the patient completed the intervention
Patient satisfaction questionnaireup to 90 days post-dischargeSatisfaction regarding intervention participation
Time to emergency room visitUp to 90 days post-dischargeNumber of days between hospital discharge and emergency room visit

Countries

Switzerland

Contacts

Primary ContactMario Ernst
mario.ernst@felixplatter.ch+41 61 326 44 81
Backup ContactIsabel Pfundstein
isabel.pfundstein@felixplatter.ch+41 61 326 44 81

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026