Implementation and Effectiveness of Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship (ENCOMPASS)
Primary Purpose
Sepsis
Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sepsis Transition and Recovery (STAR) program
Usual care
Sponsored by
About this trial
This is an interventional health services research trial for Sepsis focused on measuring evidence based medicine, transition care, critical care, implementation science, pragmatic clinical trial
Eligibility Criteria
Inclusion Criteria:
- At least 18 years of age upon admission
Suspected infection
- Oral/parenteral antibiotic or bacterial culture order within 24 hours of emergency department presentation; and
- Evidence of systemic inflammatory response (i.e., at least two abnormal of temperature; heart rate; respiratory rate; and WBC count or bands)
- Evidence of organ dysfunction (i.e., at least two points on either Quick Sepsis-related Organ Failure Assessment or Sepsis-related Organ Failure Assessment risk tools)
- Deemed as high risk for 90-day readmission using risk-scoring models
- Not discharged at the time of patient list generation
Exclusion Criteria:
- Patients with a change in code status (i.e., do not resuscitate, do not intubate) within 24 hours after infection onset due to presumed limitation of aggressive treatment
- Patients who reside > 2.5 hours drive time from the treating hospital
- Patients actively enrolled in a different care management program at time of admission
- Patient has been randomized previously.
Sites / Locations
- Atrium Health
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Sepsis Transition and Recovery (STAR) Program
Usual Care
Arm Description
Virtual sepsis navigation delivered across the peri-hospital discharge interval
Standard of care received through Atrium Health facilities for patients hospitalized with sepsis. Aspects of usual care will be determined by treating clinicians independent of trial assignment.
Outcomes
Primary Outcome Measures
All-cause mortality and hospital readmission rate
Binary composite endpoint of mortality and hospital readmission assessed 90 days post index hospital discharge
Secondary Outcome Measures
Number of days alive and outside the hospital
Continuous composite endpoint of days alive and outside of the hospital assessed 90 days post index hospital discharge
All-cause mortality rate
Binary endpoint of all-cause mortality rate assessed 90 days post index hospital discharge
All-cause hospital readmission rate
Binary endpoint of all-cause hospital readmission rate assessed 90 days post index hospital discharge
Number of outpatient provider visits
Number of outpatient provider visits assessed 90 days post index hospital discharge
Number of emergency department visits
Number of emergency department visits assessed 90 days post index hospital discharge
Cause-specific hospital readmission rate
Binary endpoint of cause-specific readmission rate for infection, chronic lung disease, heart failure, acute renal failure, and ambulatory care sensitive conditions assessed 90 days post index hospital discharge
Full Information
NCT ID
NCT04495946
First Posted
July 7, 2020
Last Updated
October 6, 2023
Sponsor
Wake Forest University Health Sciences
Collaborators
National Institute of Nursing Research (NINR)
1. Study Identification
Unique Protocol Identification Number
NCT04495946
Brief Title
Implementation and Effectiveness of Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship
Acronym
ENCOMPASS
Official Title
Implementation and Effectiveness of Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship: A Hybrid Effectiveness-Implementation Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 1, 2020 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
April 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
Collaborators
National Institute of Nursing Research (NINR)
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
The purpose of this study is to evaluate if implementation of the Sepsis Transition and Recovery (STAR) program within a large healthcare system will improve outcomes for high-risk patients with suspected sepsis, while concurrently examining contextual factors related to STAR program delivery within routine care to generate knowledge of best practices for implementation and dissemination of post sepsis transitions of care. To address persistent morbidity and mortality for sepsis survivors, Atrium Health developed the Sepsis Treatment and Recovery (STAR) program which uses a nurse navigator to deliver a bundle of best-practice care elements for the delivery of longitudinal post-sepsis care for up to 90 days. These care elements are directed towards the specific challenges and sequelae following a sepsis hospitalization and include: 1) identification and treatment of new physical, mental, and cognitive deficits; 2) review and adjustment of medications; 3) surveillance of treatable conditions that commonly lead to poor outcomes including chronic conditions that may de-stabilize during sepsis and recovery; and 4) focus on palliative care when appropriate. ENCOMPASS (Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship) is an effectiveness-implementation hybrid type I trial, with the evaluation designed as a two-arm, pragmatic, stepped-wedge cluster randomized controlled trial conducted at eight regional hospitals in which each participating hospital begins in a usual care control phase and transitions to the STAR program intervention in a randomly assigned sequence. Patients are allocated to receive the treatment condition (i.e., usual care or STAR) assigned to their admission hospital at time of enrollment. ENCOMPASS will test the hypothesis that patients who receive care through the STAR program will have reduced mortality and hospital readmission assessed 90 days post index hospital discharge compared to patients who receive usual care.
Detailed Description
BACKGROUND
Sepsis is a common and life-threatening condition defined by organ dysfunction due to a dysregulated response to infection (Fleischmann, 2016). Aggressive early sepsis identification and treatment initiatives have decreased hospital mortality for patients with sepsis (Rhodes, 2017; Kaukonen, 2014). However, sepsis survivors continue to face challenges after the acute illness episode, experiencing new functional, cognitive, and psychological deficits, and high rates of hospital readmission and mortality in the 90-days after hospital discharge (Iwashyna, 2010; Borges, 2015; Annane, 2015; Prescott, 2015; Mayr, 2017). To address persistent morbidity and mortality for sepsis survivors, Atrium Health developed the Sepsis Treatment and Recovery (STAR) program which uses a nurse navigator to deliver a bundle of best-practice care elements for the delivery of longitudinal post-sepsis care for up to 90 days. These care elements are directed towards the specific challenges and sequelae following a sepsis hospitalization and include: 1) identification and treatment of new physical, mental, and cognitive deficits; 2) review and adjustment of medications; 3) surveillance of treatable conditions that commonly lead to poor outcomes including chronic conditions that may destabilize during sepsis and recovery; and 4) focus on palliative care when appropriate (Prescott, 2018) These care elements have good face-validity and have shown to be associated with improved outcomes for sepsis survivors in observational data (Taylor, 2020). However, they are not widely applied in real-world settings for this vulnerable population, likely hindered by a gap in understanding key contextual factors underlying how to best integrate this bundle of care elements into the complex and fragmented post-discharge setting (Brownson, 2012; Bodenheimer, 2008; Coleman, 2004; Kim, 2013)
RATIONALE
In randomized controlled trials (RCTs), successfully implemented care transition programs using nurse navigators have been shown to reduce hospital readmission and costs. To better enhance transitions of care for the highest risk, complex patients with suspected sepsis, the investigators propose extending this evidence using a nurse-facilitated care transition program for patients in the post-sepsis transition period to improve the implementation of recommended care practices and bridge care gaps. This approach, called the Sepsis Transition and Recovery (STAR) program, is the next step in the progression of the investigator team's work on improving discharge transitions and sepsis processes of care. A key aspect of this initiative includes the ability to identify sepsis survivors at the greatest risk for poor outcomes. For example, one-quarter of sepsis survivors account for three-quarters of hospital readmission and costs, indicating that identifying high-risk sepsis patients for targeted facilitation of best-practice care could efficiently impact quality and cost.
The STAR program uses near real-time risk modeling to identify high-risk patients and a centrally located nurse, virtually connected to participating hospitals, to coordinate the application of evidence-based recommendations for post-sepsis care, overcome barriers to recommended care, and bridge gaps in service that can serve as points of failure for complex patients. During hospitalization, high-risk patients enter into a transition pathway integrated within Atrium Health Hospital Medicine's Transition Services program and includes the following core components: i) Introduction to STAR process prior to discharge (confirm provider consults e.g., PT, ID, palliative); ii) Disease-specific education and discharge "playbook"; iii) Virtual hospital follow-up evaluation within 48 hours including medication reconciliation; iv) Second, post-acute virtual follow-up within 72-96 hours (symptom monitoring, confirm provider follow-up); v) Weekly contact with STAR team; vi) Referral to provider follow-up (e.g., primary care provider, transition clinic) as appropriate; vii) Coordinated transition to the next appropriate care location after 90 days from time of discharge. The STAR navigator also meets weekly with the Medical Director of the Atrium Health Transition Services program who provides additional clinical oversight of ongoing cases.
The ENCOMPASS (Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship) evaluation will examine if implementation of the STAR program within a large healthcare system will improve outcomes for high-risk sepsis patients. This cluster randomized program evaluation is designed to be a seamless part of routine care in a real-world setting to generate knowledge of best practices for implementation and dissemination of post-sepsis transitions of care.
INVESTIGATIONAL PLAN
Overall Study Design ENCOMPASS is an effectiveness-implementation hybrid type I trial. The evaluation component is designed as a two-arm, pragmatic, stepped-wedge cluster randomized controlled trial conducted at eight regional hospitals in which each participating hospital begins in a usual care control phase and transitions to the STAR program intervention in a randomly assigned sequence, with one of eight hospitals assigned to transition at each four-month interval (i.e., step). During the time that a hospital is allocated to usual care, all eligible patients will receive usual care. Once a hospital has been allocated to the STAR arm, all eligible patients will receive STAR during their index hospitalization and extending through 90 days from discharge or date of death. The ENCOMPASS trial will compare the effectiveness of the Sepsis Transition And Recovery (STAR) program versus usual care on post-sepsis care and patient outcomes. The STAR program is informed by existing evidence and designed using the Chronic Care Model to increase best-practice adherence and care coordination, resulting in improved transitions between hospitals and post-acute care during sepsis recovery.
ENCOMPASS will test the STAR program intervention within the course of providing usual care among a large and diverse population of post-sepsis patients admitted to eight hospitals within Atrium Health, one of the largest, vertically integrated health systems in the US. The eight acute care hospitals participating in this study use the same EHR, which connects across all points of care, including outpatient practices, urgent care locations, emergency departments and hospitals. Consistent with the pragmatic study design concept, eligibility criteria are broad, the sample size is large and diverse, and study procedures are embedded into the context of routine care. To be objective in patient selection and allow for program evaluation, a data driven approach will be used to identify patients as eligible for program referral. Each weekday morning actively admitted patients at eight study hospitals will be identified from the electronic health record and Enterprise Data Warehouse and output into daily eligibility lists based on the study's inclusion/exclusion criteria. Primary analyses will be conducted using an intent-to-treat approach such that all eligible patients will be included. Planned enrollment is 4032 patients and STAR program follow-up will be completed 90 days after hospital discharge. Outcomes data will be tracked for 90 days and captured from routinely collected data from the Atrium Health Enterprise Data Warehouse. Given this evaluation protocol relies on using evidence-based interventions, only utilizes data collected as part of routine care, and is minimal risk to patients, the institutional review board granted the request for waiver of informed consent.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis
Keywords
evidence based medicine, transition care, critical care, implementation science, pragmatic clinical trial
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Pragmatic, stepped-wedge cluster randomized controlled trial
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
4018 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sepsis Transition and Recovery (STAR) Program
Arm Type
Experimental
Arm Description
Virtual sepsis navigation delivered across the peri-hospital discharge interval
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Standard of care received through Atrium Health facilities for patients hospitalized with sepsis. Aspects of usual care will be determined by treating clinicians independent of trial assignment.
Intervention Type
Behavioral
Intervention Name(s)
Sepsis Transition and Recovery (STAR) program
Intervention Description
In the STAR program intervention, a centrally located nurse navigator facilitates the application of four evidence-based core components of post-sepsis care (i.e., review of medications, new impairments, comorbidities, and palliative care) to patients prior to and during the 90 days after hospital discharge. The STAR navigator will provide telephone and EHR-based support within the hospitalization and to patients across all discharge settings with remote monitoring at specified intervals following hospital discharge. Patients will continue to receive STAR directed services for 90 days following their discharge and then will be transitioned back to the next appropriate care location.
Intervention Type
Behavioral
Intervention Name(s)
Usual care
Intervention Description
Hospitals and their patients will not have access to the STAR program. Patients will continue to receive usual care throughout their stay and discharge, consisting of: patient education and follow-up instructions at discharge, which are not specific to sepsis; routine recommendations for follow-up visits with primary care providers; arrangements for home health services or care management follow-up based on each patient's needs but not specifically tailored to the sepsis population; discharge to post-acute setting with no sepsis-specific follow-up. All aspects of usual care will be determined by treating clinicians independent of trial assignment.
Primary Outcome Measure Information:
Title
All-cause mortality and hospital readmission rate
Description
Binary composite endpoint of mortality and hospital readmission assessed 90 days post index hospital discharge
Time Frame
90 days
Secondary Outcome Measure Information:
Title
Number of days alive and outside the hospital
Description
Continuous composite endpoint of days alive and outside of the hospital assessed 90 days post index hospital discharge
Time Frame
90 days
Title
All-cause mortality rate
Description
Binary endpoint of all-cause mortality rate assessed 90 days post index hospital discharge
Time Frame
90 days
Title
All-cause hospital readmission rate
Description
Binary endpoint of all-cause hospital readmission rate assessed 90 days post index hospital discharge
Time Frame
90 days
Title
Number of outpatient provider visits
Description
Number of outpatient provider visits assessed 90 days post index hospital discharge
Time Frame
90 days
Title
Number of emergency department visits
Description
Number of emergency department visits assessed 90 days post index hospital discharge
Time Frame
90 days
Title
Cause-specific hospital readmission rate
Description
Binary endpoint of cause-specific readmission rate for infection, chronic lung disease, heart failure, acute renal failure, and ambulatory care sensitive conditions assessed 90 days post index hospital discharge
Time Frame
90 days
Other Pre-specified Outcome Measures:
Title
Cost-Effectiveness
Description
A comparison of the STAR and usual care strategies based on the incremental cost-effectiveness ratio (ICER). The ICER is defined as the difference in costs between interventions, divided by the difference in combined mortality and readmission rates
Time Frame
90 days, 1 year
Title
Qualitative assessment of the barriers to STAR program implementation
Description
Open-ended, qualitative assessment guided by the Consolidated Framework for Implementation Research to identify perceived barriers to implementing the STAR program into the peri-discharge setting. Themes will be categorized and reported as percentages of participants.
Time Frame
Pre-implementation, 8 months, 20 months, 32 months, 36 months (i.e., Post-implementation)
Title
Qualitative assessment of the facilitators to STAR program implementation
Description
Open-ended, qualitative assessment guided by the Consolidated Framework for Implementation Research to identify perceived facilitators to implementing the STAR program into the peri-discharge setting. Themes will be categorized and reported as percentages of participants.
Time Frame
Pre-implementation, 8 months, 20 months, 32 months, 36 months (i.e., Post-implementation)
Title
Number of eligible patients reached by STAR program
Description
Navigator use per eligible patients
Time Frame
8 months, 20 months, 32 months, 36 months (i.e., Post-implementation)
Title
Number of providers included in STAR program adoption
Description
Number of providers with patients enrolled
Time Frame
8 months, 20 months, 32 months, 36 months (i.e., Post-implementation)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
At least 18 years of age upon admission
Suspected infection
Oral/parenteral antibiotic or bacterial culture order within 24 hours of emergency department presentation; and
Evidence of systemic inflammatory response (i.e., at least two abnormal of temperature; heart rate; respiratory rate; and WBC count or bands)
Evidence of organ dysfunction (i.e., at least two points on either Quick Sepsis-related Organ Failure Assessment or Sepsis-related Organ Failure Assessment risk tools)
Deemed as high risk for 90-day readmission using risk-scoring models
Not discharged at the time of patient list generation
Exclusion Criteria:
Patients with a change in code status (i.e., do not resuscitate, do not intubate) within 24 hours after infection onset due to presumed limitation of aggressive treatment
Patients who reside > 2.5 hours drive time from the treating hospital
Patients actively enrolled in a different care management program at time of admission
Patient has been randomized previously.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc Kowalkowski, PhD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stephanie P Taylor, MD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Atrium Health
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28203
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
26414292
Citation
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Citation
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Implementation and Effectiveness of Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship
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