UPTAKE - Virtual Care: Virtual Home Hospital With Remote Monitoring to Reduce Acute Care Hospitalization
Acute Kidney InjuryMethod: Randomized Controlled Trial Study Duration: 3 Years Study Centre(s) University of Calgary and University of Alberta Objectives: To fill care gaps by implementing strategies to reduce length of hospital stay, readmission rates, and improve long-term outcomes after Acute Kidney Injury (AKI). Number of Participants: Three Hundred and fifty four (n=354) Diagnosis and Main Inclusion Criteria: Hospitalized adults with AKI at high risk of hospital readmission or death
Study Intervention: Multi-component Digital Health Solutions, including:
1. Computerized Clinical Decision Support (CDS) and
2. Virtual Care Delivered through Hospital at Home (VC) Duration of administration: Determined by the Patient's clinical team Reference therapy: Usual Care Statistical Analyses: Descriptive Analysis, Regression
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Participation Requirements
-
Sex:
ALL -
Eligible Ages:
18 and up
Participation Criteria
Inclusion Criteria:
* Age ≥ 18 years old.
* AKI identified in hospital using Kidney Disease Improving Global Outcomes (KDIGO) criteria17.
* Hospitalization \> 48 hours.
* LACE (L= Length patient Stay in the hospital, A= Acuity of Admission of patient in the hospital, C= Comorbidity and E= Emergency Visit.) Score 12 or higher.
* Meets all inclusion criteria of Virtual Home Hospital programs of Calgary and Edmonton zones.
Exclusion Criteria:
* Non-Alberta residents.
* Resides outside the catchment areas for the Calgary and Edmonton Virtual Home Hospital programs.
* C1 or C2 goals of care.
* Hospitalization \> 30 days.
* Will be discharged to long-term care.
* Kidney failure receiving dialysis.
* Already admitted in Virtual Home Hospital Program
Study Location
University of Alberta
University of AlbertaEdmonton, Alberta
Canada
Contact Study Team
University of Calgary
University of CalgaryCalgary, Alberta
Canada
Contact Study Team
- Study Sponsored By
- University of Calgary
- Participants Required
- More Information
- Study ID:
NCT06537453