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Cardiac Care Bridge trial

Cardiac Care Bridge trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON24273
Enrollment
500
Registered
2017-04-06
Start date
2017-06-06
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Elderly, aged, older, geriatric, functional decline, functional loss, cadiovascular disease, heart failure, acute myocardial infarction, transitional care, disease management, case management, home-based cardiac rehabilitation, readmission, rehospitalization, mortality Ouderen, geriatrie, functionele achteruitgang, functieverlies, cardiovasculaire aandoeiningen, hartfalen, acuut myocardinfarct, transmurale zorg, diseasemanagement, casemanagement, hartrevalidatie, heropname, overlijden

Interventions

Patients admitted to the department of cardiology or cardiac surgery of > 70 years, at high risk of functional loss and admitted > 48 hours are eligible for inclusion. The program combines case manage

Sponsors

Academic Medical Center (AMC), Amsterdam, The Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - 70 years and older - Admitted patients to the departments of cardiology or cardiac surgery - Admission > 48 hours - High risk of functional decline according to the VMS screening-tool for frailty of the Dutch Safety Management Program (screening on ADL-functioning, fall risk, malnutrition and delirium): score >=2 in patients aged 70-79 years and score >= 1 in patients aged 80 years and older - Mini-Mental State Examination Score (MMSE) >= 15 - Per 28 February 2018, patients with an unplanned hospital admission in the previous six months are also eligible for inclusion (independent of the score on the VMS screening tool for frailty)

Exclusion criteria

Exclusion criteria: - Congenital heart disease - Terminal illness: defined as a life expectancy of less than three months, for example because of cancer or serious heart failure. - Transferred from or planned discharge to a nursing home - Planned discharge to another hospital not participating in this study - Unable to communicate in Dutch - Delirium as confirmed by the treating physician

Design outcomes

Primary

MeasureTime frame
The incidence of the composite end-point of first all-cause unplanned hospital readmission or mortality.

Secondary

MeasureTime frame
- The incidence proportion of the composite end-point of first all-cause unplanned hospital readmission or mortality - ADL-functioning and iADL-functioning - Functional capacity - Medication adherence - Anxiety - Depression - Health-related quality of life - Healthcare utilization - Caregiver burden

Contacts

Public ContactBianca Buurman

Postbus 22660

b.m.vanes@amc.nl+31 (0)20 5665991

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)