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Implementation and Effectiveness of Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship

Implementation and Effectiveness of Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship: A Hybrid Effectiveness-Implementation Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04495946
Acronym
ENCOMPASS
Enrollment
3894
Registered
2020-08-03
Start date
2020-07-01
Completion date
2024-04-01
Last updated
2025-09-19

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

Conditions

Sepsis

Keywords

evidence based medicine, transition care, critical care, implementation science, pragmatic clinical trial

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.

Interventions

BEHAVIORALSepsis Transition and Recovery (STAR) program

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.

BEHAVIORALUsual care

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.

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Pragmatic, stepped-wedge cluster randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. At least 18 years of age upon admission 2. Suspected infection 1. Oral/parenteral antibiotic or bacterial culture order within 24 hours of emergency department presentation; and 2. Evidence of systemic inflammatory response (i.e., at least two abnormal of temperature; heart rate; respiratory rate; and WBC count or bands) 3. 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) 4. Deemed as high risk for 90-day readmission using risk-scoring models 5. Not discharged at the time of patient list generation

Exclusion criteria

1. 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 2. Patients who reside \> 2.5 hours drive time from the treating hospital 3. Patients actively enrolled in a different care management program at time of admission 4. Patient has been randomized previously.

Design outcomes

Primary

MeasureTime frameDescription
All-cause Mortality and Hospital Readmission Rate90 daysCombined death or unplanned hospital readmission due to any cause, assessed 90 days after the index hospital discharge

Secondary

MeasureTime frameDescription
All-cause Mortality Rate90 daysPatients with date of death prior to 90 days post discharge documented in the electronic health record or in linked national death records
All-cause Hospital Readmission Rate90 daysAny hospital readmission, including both inpatient and observation status hospitalizations, assessed 90 days post index hospital discharge.
Number of Outpatient Provider Visits90 daysNumber of outpatient provider visits assessed 90 days post index hospital discharge
Number of Emergency Department Visits90 daysNumber of emergency department visits assessed 90 days post index hospital discharge
Cause-specific Hospital Readmission Rate90 daysAny hospital readmission due to sepsis or other infection conditions assessed 90 days post index hospital discharge
Inpatient Functional Assessment or Physical Therapy ConsultIndex hospital dischargeDocumented inpatient functional assessment or physical therapy consult completed and captured from electronic health records
Inpatient Mental Health AssessmentIndex hospital dischargeDocumented inpatient mental health assessment completed and captured from electronic health records
Number of Days Alive and Outside the Hospital90 daysThe total days alive without inpatient, observation, and emergency department care utilization beginning with the day of index hospital admission and ending 90 days after discharge or on the date of death if prior to 90 days.
Early Outpatient Provider Follow up7 days after dischargeThe completion of hospital follow-up visit with an outpatient provider within 7 days of hospital discharge captured from electronic health records
Outpatient Medication Reconciliation90 days after hospital dischargeCompletion of medication reconciliation in the electronic health record during the 90 days post hospital discharge
Palliative Care ConsultationIndex hospital dischargeDocumented completion of palliative care consult captured from electronic health records.
Completed Care PreferencesIndex hospital dischargeDocumented completion of patient care preferences form captured from electronic health records
Discharge to Hospice CareIndex hospital dischargeDischarge disposition of hospice care from initial sepsis hospitalization captured from electronic health records
Place of Death90 days after hospital dischargeIn-hospital, hospice, and home or other location of death captured from electronic health records
Count of Participants With Support Service Referrals90 days after hospital dischargeOutpatient rehabilitation or physical, occupational, or speech therapy during follow-up

Countries

United States

Participant flow

Recruitment details

This is a 36-month stepped-wedge cluster randomized trial. Each hospital begins enrolling patients under usual care and transitions to enrolling patients in STAR program one hospital at a time in a randomly determined sequence every 4 months. The randomization sequence was concealed to all hospitals until 1 month before each individual hospital transitioned to receive the STAR program. The trial was conducted at 7 hospitals in the Atrium Health system and one additional outside hospital.

Pre-assignment details

The outside hospital affiliated with a different health system withdrew from the trial after randomization but prior to receiving the intervention. The number of participants to start a Period is not equal to the number who completed the previous Period since this is a pragmatic trial with cross-sectional sampling of eligible patients in each step at each participating study site.

Participants by arm

ArmCount
Sepsis Transition and Recovery (STAR) Program
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.
2,122
Usual Care
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.
1,426
Total3,548

Baseline characteristics

CharacteristicTotalSepsis Transition and Recovery (STAR) ProgramUsual Care
Age, Continuous65.56 years
STANDARD_DEVIATION 15.19
65.65 years
STANDARD_DEVIATION 15.07
65.44 years
STANDARD_DEVIATION 15.37
Race (NIH/OMB)
American Indian or Alaska Native
12 Participants8 Participants4 Participants
Race (NIH/OMB)
Asian
30 Participants26 Participants4 Participants
Race (NIH/OMB)
Black or African American
867 Participants499 Participants368 Participants
Race (NIH/OMB)
More than one race
22 Participants12 Participants10 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
1 Participants1 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
48 Participants39 Participants9 Participants
Race (NIH/OMB)
White
2568 Participants1537 Participants1031 Participants
Sequential Organ Failure Assessment (SOFA) score4.637 units on a scale
STANDARD_DEVIATION 2.464
4.635 units on a scale
STANDARD_DEVIATION 2.521
4.647 units on a scale
STANDARD_DEVIATION 2.378
Sex: Female, Male
Female
1843 Participants1056 Participants787 Participants
Sex: Female, Male
Male
1705 Participants1066 Participants639 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
367 / 2,122292 / 1,426
other
Total, other adverse events
0 / 2,1220 / 1,426
serious
Total, serious adverse events
763 / 2,122478 / 1,426

Outcome results

Primary

All-cause Mortality and Hospital Readmission Rate

Combined death or unplanned hospital readmission due to any cause, assessed 90 days after the index hospital discharge

Time frame: 90 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramAll-cause Mortality and Hospital Readmission Rate1023 Participants
Usual CareAll-cause Mortality and Hospital Readmission Rate684 Participants
Secondary

All-cause Hospital Readmission Rate

Any hospital readmission, including both inpatient and observation status hospitalizations, assessed 90 days post index hospital discharge.

Time frame: 90 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramAll-cause Hospital Readmission Rate763 Participants
Usual CareAll-cause Hospital Readmission Rate478 Participants
Secondary

All-cause Mortality Rate

Patients with date of death prior to 90 days post discharge documented in the electronic health record or in linked national death records

Time frame: 90 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramAll-cause Mortality Rate367 Participants
Usual CareAll-cause Mortality Rate292 Participants
Secondary

Cause-specific Hospital Readmission Rate

Any hospital readmission due to sepsis or other infection conditions assessed 90 days post index hospital discharge

Time frame: 90 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramCause-specific Hospital Readmission Rate370 Participants
Usual CareCause-specific Hospital Readmission Rate222 Participants
Secondary

Completed Care Preferences

Documented completion of patient care preferences form captured from electronic health records

Time frame: Index hospital discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramCompleted Care Preferences526 Participants
Usual CareCompleted Care Preferences309 Participants
Secondary

Count of Participants With Support Service Referrals

Outpatient rehabilitation or physical, occupational, or speech therapy during follow-up

Time frame: 90 days after hospital discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramCount of Participants With Support Service Referrals594 Participants
Usual CareCount of Participants With Support Service Referrals374 Participants
Secondary

Discharge to Hospice Care

Discharge disposition of hospice care from initial sepsis hospitalization captured from electronic health records

Time frame: Index hospital discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramDischarge to Hospice Care97 Participants
Usual CareDischarge to Hospice Care69 Participants
Secondary

Early Outpatient Provider Follow up

The completion of hospital follow-up visit with an outpatient provider within 7 days of hospital discharge captured from electronic health records

Time frame: 7 days after discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramEarly Outpatient Provider Follow up468 Participants
Usual CareEarly Outpatient Provider Follow up348 Participants
Secondary

Inpatient Functional Assessment or Physical Therapy Consult

Documented inpatient functional assessment or physical therapy consult completed and captured from electronic health records

Time frame: Index hospital discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramInpatient Functional Assessment or Physical Therapy Consult1768 Participants
Usual CareInpatient Functional Assessment or Physical Therapy Consult1196 Participants
Secondary

Inpatient Mental Health Assessment

Documented inpatient mental health assessment completed and captured from electronic health records

Time frame: Index hospital discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramInpatient Mental Health Assessment2048 Participants
Usual CareInpatient Mental Health Assessment1385 Participants
Secondary

Number of Days Alive and Outside the Hospital

The total days alive without inpatient, observation, and emergency department care utilization beginning with the day of index hospital admission and ending 90 days after discharge or on the date of death if prior to 90 days.

Time frame: 90 days

ArmMeasureValue (MEAN)
Sepsis Transition and Recovery (STAR) ProgramNumber of Days Alive and Outside the Hospital72.2 Days
Usual CareNumber of Days Alive and Outside the Hospital71.9 Days
Secondary

Number of Emergency Department Visits

Number of emergency department visits assessed 90 days post index hospital discharge

Time frame: 90 days

ArmMeasureValue (MEAN)
Sepsis Transition and Recovery (STAR) ProgramNumber of Emergency Department Visits0.50 count of visits
Usual CareNumber of Emergency Department Visits0.46 count of visits
Secondary

Number of Outpatient Provider Visits

Number of outpatient provider visits assessed 90 days post index hospital discharge

Time frame: 90 days

ArmMeasureValue (MEAN)
Sepsis Transition and Recovery (STAR) ProgramNumber of Outpatient Provider Visits3.0 count of visits
Usual CareNumber of Outpatient Provider Visits3.6 count of visits
Secondary

Outpatient Medication Reconciliation

Completion of medication reconciliation in the electronic health record during the 90 days post hospital discharge

Time frame: 90 days after hospital discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramOutpatient Medication Reconciliation1590 Participants
Usual CareOutpatient Medication Reconciliation866 Participants
Secondary

Palliative Care Consultation

Documented completion of palliative care consult captured from electronic health records.

Time frame: Index hospital discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramPalliative Care Consultation430 Participants
Usual CarePalliative Care Consultation234 Participants
Secondary

Place of Death

In-hospital, hospice, and home or other location of death captured from electronic health records

Time frame: 90 days after hospital discharge

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Sepsis Transition and Recovery (STAR) ProgramPlace of DeathIn hospital deaths204 Participants
Sepsis Transition and Recovery (STAR) ProgramPlace of DeathHospice deaths69 Participants
Sepsis Transition and Recovery (STAR) ProgramPlace of DeathHome or other deaths94 Participants
Usual CarePlace of DeathIn hospital deaths150 Participants
Usual CarePlace of DeathHospice deaths67 Participants
Usual CarePlace of DeathHome or other deaths75 Participants

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026