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UPTAKE: Using Personalized Risk and Digital Tools to Guide Transitions Following Acute Kidney Events (UPTAKE-1)

Primary Purpose

Acute Kidney Injury

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Risk-guided transition of care intervention delivered through an integrated digital health strategy
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Acute Kidney Injury

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: (all of) Age ≥ 18 years old Hospitalized at site using AHS EHR Acute Kidney Injury (Stage 1-3) identified in hospital per KDIGO guideline criteria Exclusion Criteria: (any of) Already under nephrologist care (CKD, dialysis, or transplant program care prior to hospital discharge) Pre-hospitalization advanced CKD: eGFR<30 mL/min/1.73m2 Low risk (<1% risk) of death or advanced CKD (based on our CKD risk prediction model51) Non-Alberta resident (without registration for Alberta health care insurance coverage) Palliative goals of care (C1/C2 per AHS framework)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Intervention

    Usual Care

    Arm Description

    The proposed experimental intervention will incorporate our risk prediction model which will be used to guide the hospital to home transition of care for medium and high-risk groups of patients. Patients will receive transition of care plans that are tailored to their risk and embedded within standardized discharge pathways within the EHR. Documentation of AKI in the discharge summary Consult for medication reconciliation Information about AKI provided to patients through EHR Sick day guidance provided to patients through EHR Kidney function testing done on day of discharge Lab requisition provided for kidney function testing at 3 months for all patients Lab requisition provided for kidney function testing at 1 month for high risk patients Follow-up appointment booked with a study nephrologist within 3 months of discharge for high risk patients If patient known to have CKD prior to admission and meets CKD referral criteria, referral to nephrology

    The usual care group will not receive the risk-guided transition of intervention and will receive standard hospital discharge care in accordance with local health system standards (Alberta Health Services), and additional requisitions for kidney function testing at 90 days.

    Outcomes

    Primary Outcome Measures

    Primary effectiveness outcome
    The primary outcome of the study is major adverse kidney or CV events at 1 year, defined as the composite of death, kidney failure (receipt of maintenance dialysis or eGFR < 15 mL/min/1.73m2 for 4 weeks or more), or hospitalization with a most responsible diagnosis for heart failure, myocardial infarction, or stroke (based on validated ICD-10 coding algorithms)

    Secondary Outcome Measures

    Secondary Clinical Outcomes-Death
    Major adverse kidney or CV events at 1 year, defined as death
    Secondary Clinical Outcomes-Kidney Failure
    Major adverse kidney or CV events at 1 year, defined as kidney failure (receipt of maintenance dialysis or eGFR < 15 mL/min/1.73m2 for 4 weeks or more)
    Secondary Clinical Outcomes-Hospitalization for CV Events
    Major adverse kidney or CV events at 1 year, defined as hospitalization with a most responsible diagnosis for heart failure, myocardial infarction, or stroke (based on validated ICD-10 coding algorithms)
    Secondary Clinical Outcomes-All Cause Hospitalization or ED Visit
    All-cause hospitalization or ED visits within 30 and 90 days of discharge
    Patient Experience
    The Care Transitions Measure (CTM) will be used to assess the hospital to home transition experience from the patient perspective. All 15 items in the CTM-15 use a 4-point scale with responses ranging from "Strongly Disagree" to "Strongly Agree." The items are scored by summing the responses (between 1 and 4) followed by linear transformation to a 0-to-100 range. This score reflects the quality of the care transition with lower scores indicating a poorer quality transition and higher scores indicating a better transition.
    Implementation and Process of Care Outcomes
    The success of implementation of the proposed intervention will be evaluated based on metrics linked to the RE-AIM dimensions of our implementation plan. Implementation outcomes will include the proportion of eligible patients included in the study from each facility and the proportion who received each element of the transition of care intervention according to their risk status. We will evaluate the effect of the intervention on the proportion of patients who receive recommended kidney function monitoring (eGFR, albuminuria) at 30 and 90 days after discharge, guideline-indicated medication use for kidney disease and associated conditions (RAAS blockers, SGLT-2 inhibitors, and statin use), and the proportion of patients with sustained eGFR<30 mL/min/1.73m2 who are referred to nephrology and those that actually receive a nephrology consult within 1 year.

    Full Information

    First Posted
    March 22, 2023
    Last Updated
    October 9, 2023
    Sponsor
    University of Alberta
    Collaborators
    Canadian Institutes of Health Research (CIHR), Alberta Health services
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05806645
    Brief Title
    UPTAKE: Using Personalized Risk and Digital Tools to Guide Transitions Following Acute Kidney Events
    Acronym
    UPTAKE-1
    Official Title
    UPTAKE: Using Personalized Risk and Digital Tools to Guide Transitions Following Acute Kidney Events- A Pragmatic Randomized Controlled Trial in Connect Care
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 2, 2024 (Anticipated)
    Primary Completion Date
    September 2027 (Anticipated)
    Study Completion Date
    September 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Alberta
    Collaborators
    Canadian Institutes of Health Research (CIHR), Alberta Health services

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Nearly one in ten people who are hospitalized in Canada develop a complication with sudden loss of kidney function, called acute kidney injury (AKI). AKI may lead to other severe health problems after discharge home, such as kidney failure requiring dialysis treatment, heart failure, heart attacks, stroke, and even premature death. Discharge from hospital to home can be a difficult transition where there are often gaps in identification, communication, care coordination, education, and planning of care for AKI. The study team will co-design and evaluate a tailored post-discharge care plan that is based on the risk of later kidney problems and uses currently available, yet untapped digital innovation to improve the health and experience of people with AKI. This study will be built into Alberta's new provincial electronic health record (EHR). The plan is to use digital tools in the EHR to identify all people in Alberta hospitals that have had an AKI event and are at increased risk of long-term complications. Half will randomly be assigned to receive a tailored care plan based on their risk at hospital discharge while the other half will receive care as it is currently provided by their healthcare team. The electronic health system will automatically calculate a patient's risk and report this risk in their chart along with recommendations for care. The study team includes patients, healthcare providers, and health system decision makers needed to co-develop the proposed strategy and introduce the changes needed to deliver this intervention. The investigators will study whether this strategy can reduce health problems that may happen after AKI including death, need for dialysis, heart attacks, and stroke. The investigators will also determine if the approach improves patient experience during the transition from hospital to home. This study has the potential to revolutionize how we care for people that leave hospital after having AKI.
    Detailed Description
    Acute kidney injury (AKI) is common in hospitalized patients and associated with poor long-term outcomes including kidney failure, cardiovascular (CV) events, and death, with highest risk in older adults. The transition of hospitalized patients with AKI to home is challenging, with many care gaps. Identifying those at highest risk of adverse post-discharge outcomes and delivering interventions to reduce the risk of progressive kidney and CV disease via appropriate, acceptable, and efficient intervention strategies are needed. Our team has developed and externally validated a risk prediction model for hospitalized adults with AKI, which can estimate the risk of major adverse kidney and cardiovascular events and death. The investigators used this risk model to guide follow-up in a pilot trial for AKI survivors within Alberta (ClinicalTrials.gov: NCT02915575). The investigators have found that a risk-guided strategy to follow-up is a feasible approach to close gaps in care; however, larger studies are required to evaluate broader implementation, and impact on patient-centered outcomes, costs, and sustainability in a real-world setting. Alberta Health Services (AHS) is currently implementing a new province-wide clinical information system which provides a unique opportunity to use digital health technology to design and evaluate a risk-guided hospital-to-home transition of care intervention that builds upon previous work. OBJECTIVES AND METHODS: To co-develop a risk-guided intervention with patients, clinicians, and health system decision-makers to improve personalized transitions of care between hospital and home for survivors of AKI. The investigators will use a participatory research approach that engages patients and care providers to co-design an evidence-guided, experience-based intervention for AKI transitions in care. Qualitative methods will be used to identify and prioritize transition interventions aligned with patient risk of adverse post-discharge outcomes. To a) identify key service delivery supports required to integrate the AKI hospital to home transition of care intervention and b) establish usability and acceptability of the intervention within the electronic health record. With the support of the AHS and existing hospital to home transition initiatives, the investigators will work with key health system partners to integrate developed AKI transition of care intervention within the EHR. The investigators will use a mixed methods approach to identify barriers and enablers to implementation and establish usability and acceptability of the intervention. To evaluate the effectiveness of this intervention in a pragmatic clinical trial that will measure implementation success and impact on patient experience, outcomes, and costs. Using the EHR, hospitalized adults with AKI at increased risk of adverse long-term outcomes will be randomized to the risk-guided transition intervention or usual care. The risk-guided arm will receive the interventions identified in Objective 1 tailored to estimated risk from the prediction model. The primary outcome of the trial is the one-year risk of a composite of death, kidney failure, or major CV event. 6,046 patients are required to detect a 15% relative risk reduction of the primary outcome, with 90% power. Effects on patient experience, processes of care, implementation, and costs will also be evaluated.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Kidney Injury

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    InvestigatorOutcomes Assessor
    Masking Description
    This is a waiver of consent trial, participants will be randomized to an enhanced discharge care pathway vs usual care in the electronic health record.
    Allocation
    Randomized
    Enrollment
    6046 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention
    Arm Type
    Experimental
    Arm Description
    The proposed experimental intervention will incorporate our risk prediction model which will be used to guide the hospital to home transition of care for medium and high-risk groups of patients. Patients will receive transition of care plans that are tailored to their risk and embedded within standardized discharge pathways within the EHR. Documentation of AKI in the discharge summary Consult for medication reconciliation Information about AKI provided to patients through EHR Sick day guidance provided to patients through EHR Kidney function testing done on day of discharge Lab requisition provided for kidney function testing at 3 months for all patients Lab requisition provided for kidney function testing at 1 month for high risk patients Follow-up appointment booked with a study nephrologist within 3 months of discharge for high risk patients If patient known to have CKD prior to admission and meets CKD referral criteria, referral to nephrology
    Arm Title
    Usual Care
    Arm Type
    No Intervention
    Arm Description
    The usual care group will not receive the risk-guided transition of intervention and will receive standard hospital discharge care in accordance with local health system standards (Alberta Health Services), and additional requisitions for kidney function testing at 90 days.
    Intervention Type
    Other
    Intervention Name(s)
    Risk-guided transition of care intervention delivered through an integrated digital health strategy
    Intervention Description
    The proposed experimental intervention will incorporate our risk prediction model which will be used to guide the hospital to home transition of care for medium and high-risk groups of patients. Patients will receive transition of care plans that are tailored to their risk and embedded within standardized discharge pathways within the electronic health record
    Primary Outcome Measure Information:
    Title
    Primary effectiveness outcome
    Description
    The primary outcome of the study is major adverse kidney or CV events at 1 year, defined as the composite of death, kidney failure (receipt of maintenance dialysis or eGFR < 15 mL/min/1.73m2 for 4 weeks or more), or hospitalization with a most responsible diagnosis for heart failure, myocardial infarction, or stroke (based on validated ICD-10 coding algorithms)
    Time Frame
    1 year
    Secondary Outcome Measure Information:
    Title
    Secondary Clinical Outcomes-Death
    Description
    Major adverse kidney or CV events at 1 year, defined as death
    Time Frame
    1 year
    Title
    Secondary Clinical Outcomes-Kidney Failure
    Description
    Major adverse kidney or CV events at 1 year, defined as kidney failure (receipt of maintenance dialysis or eGFR < 15 mL/min/1.73m2 for 4 weeks or more)
    Time Frame
    1 year
    Title
    Secondary Clinical Outcomes-Hospitalization for CV Events
    Description
    Major adverse kidney or CV events at 1 year, defined as hospitalization with a most responsible diagnosis for heart failure, myocardial infarction, or stroke (based on validated ICD-10 coding algorithms)
    Time Frame
    1 year
    Title
    Secondary Clinical Outcomes-All Cause Hospitalization or ED Visit
    Description
    All-cause hospitalization or ED visits within 30 and 90 days of discharge
    Time Frame
    30 and 90 days of discharge
    Title
    Patient Experience
    Description
    The Care Transitions Measure (CTM) will be used to assess the hospital to home transition experience from the patient perspective. All 15 items in the CTM-15 use a 4-point scale with responses ranging from "Strongly Disagree" to "Strongly Agree." The items are scored by summing the responses (between 1 and 4) followed by linear transformation to a 0-to-100 range. This score reflects the quality of the care transition with lower scores indicating a poorer quality transition and higher scores indicating a better transition.
    Time Frame
    1 year
    Title
    Implementation and Process of Care Outcomes
    Description
    The success of implementation of the proposed intervention will be evaluated based on metrics linked to the RE-AIM dimensions of our implementation plan. Implementation outcomes will include the proportion of eligible patients included in the study from each facility and the proportion who received each element of the transition of care intervention according to their risk status. We will evaluate the effect of the intervention on the proportion of patients who receive recommended kidney function monitoring (eGFR, albuminuria) at 30 and 90 days after discharge, guideline-indicated medication use for kidney disease and associated conditions (RAAS blockers, SGLT-2 inhibitors, and statin use), and the proportion of patients with sustained eGFR<30 mL/min/1.73m2 who are referred to nephrology and those that actually receive a nephrology consult within 1 year.
    Time Frame
    30 and 90 days after discharge, within 1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: (all of) Age ≥ 18 years old Hospitalized at site using AHS EHR Acute Kidney Injury (Stage 1-3) identified in hospital per KDIGO guideline criteria Exclusion Criteria: (any of) Already under nephrologist care (CKD, dialysis, or transplant program care prior to hospital discharge) Pre-hospitalization advanced CKD: eGFR<30 mL/min/1.73m2 Low risk (<1% risk) of death or advanced CKD (based on our CKD risk prediction model51) Non-Alberta resident (without registration for Alberta health care insurance coverage) Palliative goals of care (C1/C2 per AHS framework)
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Neesh Pannu
    Phone
    780 492 8519
    Email
    npannu@ualberta.ca
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Neesh Pannu
    Organizational Affiliation
    University of Alberta
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

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