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Transitional CareAdvantAGENCT06190288

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

A study testing Transitional care model in people with Transitional Care and Multimorbidity, run by Thekla Brunkert at 1 site in Switzerland.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 65 years and older
Conditions the study is for
Transitional Care, Multimorbidity, Geriatric Care
What is being tested?
Transitional care model
Could I receive a placebo?
No, everyone receives an active treatment
How many people
250 participants
Where
1 siteSwitzerland
Study dates
8 Jan 2024to 30 Jun 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 years and older
  • All sexes
  • No healthy volunteers
  • Older adult

Who may be able to join

  • 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
Show all 10Show fewer
  • 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.

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Switzerland1 site, 1 recruiting
  • Universitäre Altersmedizin FELIX PLATTER

    Basel, 4055

    Mario Ernst, MSc, +41613264481, mario.ernst@felixplatter.ch

    Recruiting

Other trials in Switzerland

About this study

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

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.

Being tested
Transitional care model
Keywords
Transitional Care, Frailty, Rehospitalisation, Geratric Care
Medical subject headings
Frailty

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Transitional care modelOther

    Also called AdvantAGE

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

Study groups in NCT06190288
Study groupRoleWhat they receive
Intervention groupExperimentalThe intervention includes five core elements provided by a multiprofessional team: (1) continuous support for patients and caregivers; (2) care coordination with primary care providers;(3) visits at patients' homes; (4) medication- and self-management with patients and caregivers; and (5) proactive advanced care planning. Patients will receive specialized support including home visits up to 90 days after hospital discharge.
Receives: Other: Transitional care model

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 90-days rehospitalization rate

    Number of unplanned hospital admissions of any kind happening within 90 days after discharge

    Measured: 90 days post-discharge

Secondary outcomes (6)
  1. 30-days rehospitalization rate

    Number of unplanned hospital admission of any kind happening within 30 days after discharge

    Measured: 30 days post-discharge

  2. Time to readmission

    Number of days between hospital discharge and unplanned hospital admission

    Measured: Up to 90 days post-discharge

  3. Number of emergency room visits

    Number of emergency room visits (with or without hospital admission) within 90 days after discharge

    Measured: 90 days post-discharge

  4. Time to emergency room visit

    Number of days between hospital discharge and emergency room visit

    Measured: Up to 90 days post-discharge

  5. Patient's health-related quality of life

    The 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

    Measured: Up to 90 days post-discharge

  6. Patient satisfaction questionnaire

    Satisfaction regarding intervention participation

    Measured: up to 90 days post-discharge

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Jan 2024
  2. Study start8 Jan 2024
  3. Primary completion30 Jun 2026 (estimated)
  4. Study completion30 Jun 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Model description
Hybrid effectiveness-implementation study (type 1)
Masking
None (open label)
Enrolment
250 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06190288
Sponsor's protocol ID
02072
Acronym
AdvantAGE
Status last verified
Feb 2024
First submitted
19 Dec 2023
Last updated
2 Feb 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Brunkert T, Pfundstein I, Nickel CH, Lampert ML, Trutschel D, Mauthner O. AdvantAGE: Implementation and Evaluation of an Interprofessional Transitional Care Model for Frail Older Adults-Protocol of an Effectiveness-Implementation Hybrid Study. J Adv Nurs. 2025 Aug;81(8):5130-5142. doi: 10.1111/jan.16745. Epub 2025 Jan 26.

    PubMed 39865439

Questions about this trial

What is this clinical trial studying?

A study testing Transitional care model in people with Transitional Care and Multimorbidity, run by Thekla Brunkert at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 2 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Mario Ernst (+41 61 326 44 81, mario.ernst@felixplatter.ch), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

90-days rehospitalization rate (time frame: 90 days post-discharge). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06190288, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Feb 2024.

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