Comprehensive Post-Acute Stroke Services (COMPASS)
Primary Purpose
Stroke, Transient Ischemic Attack
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
COMPASS Intervention
Sponsored by
About this trial
This is an interventional health services research trial for Stroke focused on measuring Early Supported Discharge, Transitional Care, Post-acute Stroke Care, Pragmatic Trial, Recovery and Rehabilitation, Secondary Prevention
Eligibility Criteria
Inclusion Criteria:
- English and Spanish speaking stroke patients with diagnosis of ischemic stroke, hemorrhagic stroke or TIA who are discharged home from participating hospitals
- Must be 18 years of age and older at the time of the stroke
Exclusion Criteria:
- Excludes subdural or aneurysmal subarachnoid hemorrhage
Sites / Locations
- CHS Stanly
- Mission Hospital
- UNC Hospital
- CHS Carolinas Medical Center
- Novant Health Presbyterian Medical Center
- CHS Carolinas Medical Center-Mercy
- CHS University
- CHS Northeast
- Betsy Johnson Hospital
- Morehead Memorial Hospital
- Hugh Chatham Memorial Hospital
- Cape Fear Valley Medical Center
- Angel Medical Center
- Pardee Health
- Frye Regional Medical Center
- Novant Health Huntersville
- Onslow Memorial Hospital
- Ashe Memorial Hospital
- Vidant Duplin Hospital
- CHS Kings Mountain
- Lenoir Memorial Hospital
- Caldwell Memorial Hospital
- WFBH Lexington Medical Center
- CHS Lincoln
- Novant Health Matthews Medical Center
- CHS Union
- Carteret County General Hospital
- CHS Blue Ridge
- Northern Hospital of Surry County
- Wilkes Regional Medical Center
- FirstHealth Moore Regional
- Washington County Hospital
- UNC Rex Healthcare
- Duke Raleigh Hospital
- WakeMed Health and Hospital
- CHS Cleveland
- Alleghany County Memorial Hospital
- Blue Ridge Regional Hospital
- Vidant Edgecombe Hospital
- New Hanover Regional Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
Usual Care
COMPASS Intervention
Arm Description
Participating hospitals randomized to the usual care group will provide their usual, post-acute stroke care to their patients.
Participating hospitals randomized to the intervention will change the structure and process for delivery of post-acute stroke care.
Outcomes
Primary Outcome Measures
Stroke Impact Scale (SIS-16)
16-item survey to assess the difficulty level of performing basic physical activities; scores range from 0-100; higher scores correspond to more favorable outcomes
Secondary Outcome Measures
Modified Caregiver Strain Index
13-item survey to measure strain that caregivers may experience; scores range from 0-100; higher scores indicate more caregiver burden
Self-reported General Health
Self-reported general health is a single question to rate their general health. Responses on a 5-point Likert Scale (Excellent, Very Good, Good, Fair, or Poor) will be analyzed as a continuous variable. Scores range from 95-15 with a higher score indicating better health.
Modified Rankin Score
to measure the degree of disability or dependence; scores range from 0-6; higher scores correspond to less favorable outcomes
Number of Participants Physically Active and Not Physically Active
Participants are asked whether they walked continuously for at least 10 minutes on any of the last seven days, how many of those days they walked continuously for at least 10 minutes and how many minutes they walked, on average, each day. The physical activity endpoint will be self-reported total number of minutes walked during the past seven days.
Number of Participants With or Without Depression
Based on answers to Patient Health Questionnaire 2-Item (PHQ-2) which is a 2-item questionnaire to determine the frequency of depressed mood; scores range from 0-6; higher scores correspond to less favorable outcomes
Cognition (MoCA 5-min Protocol)
4-item questionnaire to determine vascular cognitive impairment; scores range from 0-30; higher scores are more favorable
Medication Adherence (Morisky Green Levine Scale-4)
4 items with yes/no response options; scores range from 0-4; higher scores correspond to less medication adherence
Number of Participants With or Without Falls
Participants are asked 4 questions to determine whether they have fallen (yes versus no) since hospital discharge, whether or not the fall resulted in a doctor/emergency room visit, whether they have fallen multiple times since discharge, and how many times they have fallen since discharge. Analysis of falls will be based on incidence of any fall since hospital discharge (no falls versus at least one fall).
Self-reported Fatigue (PROMIS Fatigue Instrument)
4-question instrument to determine level of fatigue; higher scores correspond to less favorable outcomes; The total raw score is obtained by summing individual question scores and has a range of 4-20. For analysis, raw scores are translated into T-scores which range from 33.7 - 75.8. The T-score rescales the raw score into a standardized score with a mean of 50 and a SD of 10.
Satisfaction With Care
6 questions to determine satisfaction with care; scores range from 0-100; higher scores correspond to higher satisfaction of care
Number of Participants Who Do or Do Not Monitor Blood Pressure at Home
Participants are asked 2 questions to determine whether they monitor their blood pressure at home (yes or no) and, if they answer in the affirmative, how frequently (daily, weekly, and monthly). Home blood pressure monitoring was analyzed as a dichotomous endpoint (monitoring with any frequency versus no monitoring).
Self-reported Blood Pressure
1 question to determine self-reported blood pressure. Self-reported systolic and diastolic BP will each be analyzed as a continuous endpoint. In addition, self-reported systolic and diastolic BP will be used to create a dichotomous hypertension endpoint (systolic BP >= 140 versus systolic BP < 140).
Number of Subjects With Claims-based All-cause Hospital Readmissions
Number of Subjects With Claims-based All-cause Hospital Readmissions
Number of Subjects With Claims-based All-cause Hospital Readmissions
Number of Subjects With All-cause Mortality Using NC State Death Index
Deaths within 90 days of index discharge were ascertained from the North Carolina State Death Index as well as insurance claims beneficiary summary files (i.e. FFS Medicare). A death identified in either database is considered a death.
Number of Subjects With All-cause Mortality Using NC State Death Index & Fee-For-Service (FFS) Medicare
Deaths within 1 year of index discharge were ascertained from the North Carolina State Death Index as well as insurance claims beneficiary summary files (i.e. FFS Medicare). A death identified in either database is considered a death.
Number of Subjects With Claims-based Emergency Department Visits
Number of Subjects With Claims-based Admissions to Skilled Nursing Facilities (SNF) and Inpatient Rehabilitation Facilities (IRF)
Number of Subjects With Claims-based Use of Transitional Care Management Billing Codes
Full Information
NCT ID
NCT02588664
First Posted
October 23, 2015
Last Updated
May 17, 2021
Sponsor
Wake Forest University Health Sciences
Collaborators
University of North Carolina, Chapel Hill, Duke University, East Carolina University
1. Study Identification
Unique Protocol Identification Number
NCT02588664
Brief Title
Comprehensive Post-Acute Stroke Services
Acronym
COMPASS
Official Title
Early Supported Discharge for Improving Functional Outcomes After Stroke
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
July 25, 2016 (Actual)
Primary Completion Date
July 25, 2018 (Actual)
Study Completion Date
March 15, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
Collaborators
University of North Carolina, Chapel Hill, Duke University, East Carolina University
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 pragmatic study is to investigate whether implementation of a comprehensive post-acute stroke service model that integrates Early Supported Discharge (ESD) and Transitional Care Management (TCM) for stroke survivors discharged home improves functional outcomes post-stroke, reduces caregiver stress, and reduces readmission rates.
Detailed Description
Stroke mortality is 20-40% higher in North Carolina (NC) than in the overall United States. After discharge, stroke patients are at high risk for complications. Although a model of stroke post-care (early supported discharge) exists in Europe and Canada, it has not been adapted for and tested in the US, although patients and stakeholders attest that post-acute care does not meet their needs. Transitional care services from hospital to home are now reimbursed by Centers for Medicaid and Medicare Services (CMS), but only for 30 days after discharge. The study team proposed a pragmatic, cluster randomized trial of 41 NC hospitals to determine the effectiveness of COMprehensive Post-Acute Stroke Services (COMPASS), a patient-centered intervention uniting transitional care management services and elements of early supported discharge in stroke patients discharged directly home.
The study team will build on the successful North Carolina Stroke Care Collaborative (NCSCC) registry, a prospective stroke database in which 51 (of 113) hospitals in NC enroll patients. In preparation for COMPASS, the study team engaged these hospitals via webinars. Over 80% of NCSCC hospitals demonstrated an interest in participation and provided letters of support.
The main question of this pragmatic trial is: Does implementation of COMPASS for all stroke patients discharged directly home improve functional outcomes as measured by the Stroke Impact Scale-16 (SIS-16) at 90 days post-stroke? The primary aim is to: compare the COMPASS model versus usual care on stroke survivors' self-reported functional status at 90 days post-stroke. The secondary aims are to determine if the COMPASS model affects: (1) caregiver strain (Modified Caregiver Strain Index); (2) self-reported general health; (3) disability (Modified Rankin Score); (4) self-reported physical activity; (5) depression (PHQ-2); (6) cognition (MoCA 5-min protocol); (7) medication adherence (Morisky Green Levine Scale-4); (8) self-reported falls; (9) self-reported fatigue (PROMIS Fatigue Instrument); (10) satisfaction with care; (11) secondary prevention - home blood pressure monitoring; (12) self-reported blood pressure; (13-15) all-cause hospital readmissions at 30-days, at 90-days and at 1 year after index discharge; (16-17) mortality at 90-days and at 1 year after index discharge; (18-20) healthcare utilization (emergency department visits, admissions to skilled nursing facilities/inpatient rehabilitation facilities); and (21) use of transitional care management billing codes. This study will also evaluate the effectiveness of the COMPASS Intervention in key patient subgroups based on race, sex, age, diagnosis (stroke versus TIA), stroke severity, and type of health insurance.
English and Spanish-speaking patients ages 18 and older who are admitted to a participating hospital with a diagnosis of ischemic or hemorrhagic stroke or transient ischemic attack and discharged from acute care hospitalization to home will be included (about 6,000 patients/year).
Participating hospitals will be randomized (stratified by stroke volume and primary stroke center status) to receive COMPASS or usual care (control group) in Phase 1. In Phase 2, usual care hospitals will cross over to COMPASS, while the early intervention hospitals sustain the intervention using hospital-based resources.
The trial has three integrated intervention components: (1) COMPASS, which combines transitional care services provided by advanced practice providers (APPs) and early supported discharge services coordinated by the Post-Acute Coordinators (PAC); (2) COMPASS-funded post-acute care coordinators who will engage patient and stakeholder communities to improve post-acute stroke comprehensive stroke services; and (3) development of a stroke metrics scorecard for participating sites. Well-trained APPs and coordinators will have access to online learning and ongoing support/consultation from WFBH personnel and board-certified vascular neurologists.
The study team will assess 90-day and 1-year outcomes. Outcomes at 90-days will be assessed by telephone surveyors blinded to patient's group assignment. Patients will be informed about COMPASS in the hospital and can opt out of 90-day phone follow-up at any time. Those who agree to be surveyed will be asked to provide informed consent at the 90-day phone call to collect outcomes data.
This proposal is led by three highly experienced researchers as co-principal investigators. The team includes expertise in stroke care, large clinical trials, biostatistics, managing clinical registries, survey and acquisition of patient or proxy-reported outcomes, community-based practice improvement, building community coalitions to reduce readmissions, claims analyses, registry management, translating evidence into practice with large multi-site collaboratives, and engaging patients and stakeholders in research. The planning phase of this project has been guided by patients and stakeholders. Each community will form a community resource network to advise and support the implementation of COMPASS, provide feedback to the team, and help create sustainability. If the COMPASS model shows effectiveness, engaged patients and stakeholders will be key partners to disseminate and implement COMPASS throughout the state and beyond.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Transient Ischemic Attack
Keywords
Early Supported Discharge, Transitional Care, Post-acute Stroke Care, Pragmatic Trial, Recovery and Rehabilitation, Secondary Prevention
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
6024 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Participating hospitals randomized to the usual care group will provide their usual, post-acute stroke care to their patients.
Arm Title
COMPASS Intervention
Arm Type
Active Comparator
Arm Description
Participating hospitals randomized to the intervention will change the structure and process for delivery of post-acute stroke care.
Intervention Type
Other
Intervention Name(s)
COMPASS Intervention
Intervention Description
A Post-Acute Coordinator (PAC) will visit each patient prior to discharge from the hospital.
Patient will receive a follow-up telephone call two days after having been discharged.
7-14 days after discharge, the patient will attend post-acute stroke clinic visit and receive an assessment from an Advanced Practice Provider (APP), a brief patient-reported functional assessment to generate an individualized Care Plan, and referrals from an APP. The patient's primary caregiver will be assessed to ensure caregiver availability and ability to support the patient and the caregiver's ability to cope with the new challenges of caregiving.
Patient will receive a call at 30 and 60 days post-discharge for follow-up of functional status, recovery, risk factor management and their access or utilization of recommended services.
Primary Outcome Measure Information:
Title
Stroke Impact Scale (SIS-16)
Description
16-item survey to assess the difficulty level of performing basic physical activities; scores range from 0-100; higher scores correspond to more favorable outcomes
Time Frame
post-stroke day 90
Secondary Outcome Measure Information:
Title
Modified Caregiver Strain Index
Description
13-item survey to measure strain that caregivers may experience; scores range from 0-100; higher scores indicate more caregiver burden
Time Frame
post-stroke day 90
Title
Self-reported General Health
Description
Self-reported general health is a single question to rate their general health. Responses on a 5-point Likert Scale (Excellent, Very Good, Good, Fair, or Poor) will be analyzed as a continuous variable. Scores range from 95-15 with a higher score indicating better health.
Time Frame
post-stroke day 90
Title
Modified Rankin Score
Description
to measure the degree of disability or dependence; scores range from 0-6; higher scores correspond to less favorable outcomes
Time Frame
post-stroke day 90
Title
Number of Participants Physically Active and Not Physically Active
Description
Participants are asked whether they walked continuously for at least 10 minutes on any of the last seven days, how many of those days they walked continuously for at least 10 minutes and how many minutes they walked, on average, each day. The physical activity endpoint will be self-reported total number of minutes walked during the past seven days.
Time Frame
post-stroke day 90
Title
Number of Participants With or Without Depression
Description
Based on answers to Patient Health Questionnaire 2-Item (PHQ-2) which is a 2-item questionnaire to determine the frequency of depressed mood; scores range from 0-6; higher scores correspond to less favorable outcomes
Time Frame
post-stroke day 90
Title
Cognition (MoCA 5-min Protocol)
Description
4-item questionnaire to determine vascular cognitive impairment; scores range from 0-30; higher scores are more favorable
Time Frame
post-stroke day 90
Title
Medication Adherence (Morisky Green Levine Scale-4)
Description
4 items with yes/no response options; scores range from 0-4; higher scores correspond to less medication adherence
Time Frame
post-stroke day 90
Title
Number of Participants With or Without Falls
Description
Participants are asked 4 questions to determine whether they have fallen (yes versus no) since hospital discharge, whether or not the fall resulted in a doctor/emergency room visit, whether they have fallen multiple times since discharge, and how many times they have fallen since discharge. Analysis of falls will be based on incidence of any fall since hospital discharge (no falls versus at least one fall).
Time Frame
post-stroke day 90
Title
Self-reported Fatigue (PROMIS Fatigue Instrument)
Description
4-question instrument to determine level of fatigue; higher scores correspond to less favorable outcomes; The total raw score is obtained by summing individual question scores and has a range of 4-20. For analysis, raw scores are translated into T-scores which range from 33.7 - 75.8. The T-score rescales the raw score into a standardized score with a mean of 50 and a SD of 10.
Time Frame
post-stroke day 90
Title
Satisfaction With Care
Description
6 questions to determine satisfaction with care; scores range from 0-100; higher scores correspond to higher satisfaction of care
Time Frame
post-stroke day 90
Title
Number of Participants Who Do or Do Not Monitor Blood Pressure at Home
Description
Participants are asked 2 questions to determine whether they monitor their blood pressure at home (yes or no) and, if they answer in the affirmative, how frequently (daily, weekly, and monthly). Home blood pressure monitoring was analyzed as a dichotomous endpoint (monitoring with any frequency versus no monitoring).
Time Frame
post-stroke day 90
Title
Self-reported Blood Pressure
Description
1 question to determine self-reported blood pressure. Self-reported systolic and diastolic BP will each be analyzed as a continuous endpoint. In addition, self-reported systolic and diastolic BP will be used to create a dichotomous hypertension endpoint (systolic BP >= 140 versus systolic BP < 140).
Time Frame
post-stroke day 90
Title
Number of Subjects With Claims-based All-cause Hospital Readmissions
Time Frame
post-stroke day 30
Title
Number of Subjects With Claims-based All-cause Hospital Readmissions
Time Frame
post-stroke day 90
Title
Number of Subjects With Claims-based All-cause Hospital Readmissions
Time Frame
post-discharge year 1
Title
Number of Subjects With All-cause Mortality Using NC State Death Index
Description
Deaths within 90 days of index discharge were ascertained from the North Carolina State Death Index as well as insurance claims beneficiary summary files (i.e. FFS Medicare). A death identified in either database is considered a death.
Time Frame
post-stroke day 90
Title
Number of Subjects With All-cause Mortality Using NC State Death Index & Fee-For-Service (FFS) Medicare
Description
Deaths within 1 year of index discharge were ascertained from the North Carolina State Death Index as well as insurance claims beneficiary summary files (i.e. FFS Medicare). A death identified in either database is considered a death.
Time Frame
post-discharge year 1
Title
Number of Subjects With Claims-based Emergency Department Visits
Time Frame
post-discharge year 1
Title
Number of Subjects With Claims-based Admissions to Skilled Nursing Facilities (SNF) and Inpatient Rehabilitation Facilities (IRF)
Time Frame
post-discharge year 1
Title
Number of Subjects With Claims-based Use of Transitional Care Management Billing Codes
Time Frame
post-discharge day 14
Other Pre-specified Outcome Measures:
Title
Subgroup Analysis: Race
Description
Analyze the main endpoint of the study in white and non-white individuals
Time Frame
post-stroke day 90
Title
Subgroup Analysis: Sex
Description
Analyze the main endpoint of the study in female and male individuals
Time Frame
measured 90 days post-stroke
Title
Subgroup Analysis: Age
Description
Analyze the main endpoint of the study in <45; 45-<55; 55-<65; 65-<75; >=75 individuals
Time Frame
measured 90 days post-stroke
Title
Subgroup Analysis: Diagnosis (Stroke Versus TIA)
Description
Analyze the main endpoint of the study in stroke versus TIA individuals
Time Frame
measured 90 days post-stroke
Title
Subgroup Analysis: Stroke Severity
Description
Analyze the main endpoint of the study in NIHSS=0, NIHSS=1-4, NIHSS>4 individuals
Time Frame
measured 90 days post-stroke
Title
Subgroup Analysis: Type of Health Insurance
Description
Analyze the main endpoint of the study in insured and uninsured individuals
Time Frame
measured 90 days post-stroke
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
English and Spanish speaking stroke patients with diagnosis of ischemic stroke, hemorrhagic stroke or TIA who are discharged home from participating hospitals
Must be 18 years of age and older at the time of the stroke
Exclusion Criteria:
Excludes subdural or aneurysmal subarachnoid hemorrhage
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pamela Duncan, PhD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHS Stanly
City
Albemarle
State/Province
North Carolina
ZIP/Postal Code
28001
Country
United States
Facility Name
Mission Hospital
City
Asheville
State/Province
North Carolina
ZIP/Postal Code
28801
Country
United States
Facility Name
UNC Hospital
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27514
Country
United States
Facility Name
CHS Carolinas Medical Center
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28203
Country
United States
Facility Name
Novant Health Presbyterian Medical Center
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28204
Country
United States
Facility Name
CHS Carolinas Medical Center-Mercy
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28207
Country
United States
Facility Name
CHS University
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28265
Country
United States
Facility Name
CHS Northeast
City
Concord
State/Province
North Carolina
ZIP/Postal Code
28025
Country
United States
Facility Name
Betsy Johnson Hospital
City
Dunn
State/Province
North Carolina
ZIP/Postal Code
28334
Country
United States
Facility Name
Morehead Memorial Hospital
City
Eden
State/Province
North Carolina
ZIP/Postal Code
27288
Country
United States
Facility Name
Hugh Chatham Memorial Hospital
City
Elkin
State/Province
North Carolina
ZIP/Postal Code
28621
Country
United States
Facility Name
Cape Fear Valley Medical Center
City
Fayetteville
State/Province
North Carolina
ZIP/Postal Code
28304
Country
United States
Facility Name
Angel Medical Center
City
Franklin
State/Province
North Carolina
ZIP/Postal Code
28734
Country
United States
Facility Name
Pardee Health
City
Hendersonville
State/Province
North Carolina
ZIP/Postal Code
28791
Country
United States
Facility Name
Frye Regional Medical Center
City
Hickory
State/Province
North Carolina
ZIP/Postal Code
28601
Country
United States
Facility Name
Novant Health Huntersville
City
Huntersville
State/Province
North Carolina
ZIP/Postal Code
28078
Country
United States
Facility Name
Onslow Memorial Hospital
City
Jacksonville
State/Province
North Carolina
ZIP/Postal Code
28546
Country
United States
Facility Name
Ashe Memorial Hospital
City
Jefferson
State/Province
North Carolina
ZIP/Postal Code
28640
Country
United States
Facility Name
Vidant Duplin Hospital
City
Kenansville
State/Province
North Carolina
ZIP/Postal Code
28349
Country
United States
Facility Name
CHS Kings Mountain
City
Kings Mountain
State/Province
North Carolina
ZIP/Postal Code
28086
Country
United States
Facility Name
Lenoir Memorial Hospital
City
Kinston
State/Province
North Carolina
ZIP/Postal Code
28503
Country
United States
Facility Name
Caldwell Memorial Hospital
City
Lenoir
State/Province
North Carolina
ZIP/Postal Code
28645
Country
United States
Facility Name
WFBH Lexington Medical Center
City
Lexington
State/Province
North Carolina
ZIP/Postal Code
27292
Country
United States
Facility Name
CHS Lincoln
City
Lincolnton
State/Province
North Carolina
ZIP/Postal Code
28092
Country
United States
Facility Name
Novant Health Matthews Medical Center
City
Matthews
State/Province
North Carolina
ZIP/Postal Code
28105
Country
United States
Facility Name
CHS Union
City
Monroe
State/Province
North Carolina
ZIP/Postal Code
28112
Country
United States
Facility Name
Carteret County General Hospital
City
Morehead City
State/Province
North Carolina
ZIP/Postal Code
28557
Country
United States
Facility Name
CHS Blue Ridge
City
Morganton
State/Province
North Carolina
ZIP/Postal Code
28655
Country
United States
Facility Name
Northern Hospital of Surry County
City
Mount Airy
State/Province
North Carolina
ZIP/Postal Code
27030
Country
United States
Facility Name
Wilkes Regional Medical Center
City
North Wilkesboro
State/Province
North Carolina
ZIP/Postal Code
28659
Country
United States
Facility Name
FirstHealth Moore Regional
City
Pinehurst
State/Province
North Carolina
ZIP/Postal Code
28374
Country
United States
Facility Name
Washington County Hospital
City
Plymouth
State/Province
North Carolina
ZIP/Postal Code
27962
Country
United States
Facility Name
UNC Rex Healthcare
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27607
Country
United States
Facility Name
Duke Raleigh Hospital
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27609
Country
United States
Facility Name
WakeMed Health and Hospital
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27610
Country
United States
Facility Name
CHS Cleveland
City
Shelby
State/Province
North Carolina
ZIP/Postal Code
28150
Country
United States
Facility Name
Alleghany County Memorial Hospital
City
Sparta
State/Province
North Carolina
ZIP/Postal Code
28675
Country
United States
Facility Name
Blue Ridge Regional Hospital
City
Spruce Pine
State/Province
North Carolina
ZIP/Postal Code
28777
Country
United States
Facility Name
Vidant Edgecombe Hospital
City
Tarboro
State/Province
North Carolina
ZIP/Postal Code
27886
Country
United States
Facility Name
New Hanover Regional Medical Center
City
Wilmington
State/Province
North Carolina
ZIP/Postal Code
28401
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
De-identified data will be made available to researchers through the PCORI-Designated Repository in accordance with their Data Sharing Policy.
Citations:
PubMed Identifier
27125528
Citation
Condon C, Lycan S, Duncan P, Bushnell C. Reducing Readmissions After Stroke With a Structured Nurse Practitioner/Registered Nurse Transitional Stroke Program. Stroke. 2016 Jun;47(6):1599-604. doi: 10.1161/STROKEAHA.115.012524. Epub 2016 Apr 28.
Results Reference
background
PubMed Identifier
28649454
Citation
Gesell SB, Klein KP, Halladay J, Bettger JP, Freburger J, Cummings DM, Lutz BJ, Coleman S, Bushnell C, Rosamond W, Duncan PW. Methods guiding stakeholder engagement in planning a pragmatic study on changing stroke systems of care. J Clin Transl Sci. 2017 Apr;1(2):121-128. doi: 10.1017/cts.2016.26. Epub 2017 Feb 27.
Results Reference
background
PubMed Identifier
28716014
Citation
Duncan PW, Bushnell CD, Rosamond WD, Jones Berkeley SB, Gesell SB, D'Agostino RB Jr, Ambrosius WT, Barton-Percival B, Bettger JP, Coleman SW, Cummings DM, Freburger JK, Halladay J, Johnson AM, Kucharska-Newton AM, Lundy-Lamm G, Lutz BJ, Mettam LH, Pastva AM, Sissine ME, Vetter B. The Comprehensive Post-Acute Stroke Services (COMPASS) study: design and methods for a cluster-randomized pragmatic trial. BMC Neurol. 2017 Jul 17;17(1):133. doi: 10.1186/s12883-017-0907-1.
Results Reference
background
PubMed Identifier
29373987
Citation
Johnson AM, Jones SB, Duncan PW, Bushnell CD, Coleman SW, Mettam LH, Kucharska-Newton AM, Sissine ME, Rosamond WD. Hospital recruitment for a pragmatic cluster-randomized clinical trial: Lessons learned from the COMPASS study. Trials. 2018 Jan 26;19(1):74. doi: 10.1186/s13063-017-2434-1.
Results Reference
background
PubMed Identifier
29572814
Citation
Bushnell CD, Duncan PW, Lycan SL, Condon CN, Pastva AM, Lutz BJ, Halladay JR, Cummings DM, Arnan MK, Jones SB, Sissine ME, Coleman SW, Johnson AM, Gesell SB, Mettam LH, Freburger JK, Barton-Percival B, Taylor KM, Prvu-Bettger J, Lundy-Lamm G, Rosamond WD; COMPASS Trial.. A Person-Centered Approach to Poststroke Care: The COMprehensive Post-Acute Stroke Services Model. J Am Geriatr Soc. 2018 May;66(5):1025-1030. doi: 10.1111/jgs.15322. Epub 2018 Mar 23.
Results Reference
background
PubMed Identifier
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Andrews JE, Moore JB, Weinberg RB, Sissine M, Gesell S, Halladay J, Rosamond W, Bushnell C, Jones S, Means P, King NMP, Omoyeni D, Duncan PW; COMPASS investigators and stakeholders. Ensuring respect for persons in COMPASS: a cluster randomised pragmatic clinical trial. J Med Ethics. 2018 Aug;44(8):560-566. doi: 10.1136/medethics-2017-104478. Epub 2018 May 2.
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Duncan PW, Abbott RM, Rushing S, Johnson AM, Condon CN, Lycan SL, Lutz BJ, Cummings DM, Pastva AM, D'Agostino RB Jr, Stafford JM, Amoroso RM, Jones SB, Psioda MA, Gesell SB, Rosamond WD, Prvu-Bettger J, Sissine ME, Boynton MD, Bushnell CD; COMPASS Investigative Team. COMPASS-CP: An Electronic Application to Capture Patient-Reported Outcomes to Develop Actionable Stroke and Transient Ischemic Attack Care Plans. Circ Cardiovasc Qual Outcomes. 2018 Aug;11(8):e004444. doi: 10.1161/CIRCOUTCOMES.117.004444.
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Bettger JP, Jones SB, Kucharska-Newton AM, Freburger JK, Coleman SW, Mettam LH, Sissine ME, Gesell SB, Bushnell CD, Duncan PW, Rosamond WD. Meeting Medicare requirements for transitional care: Do stroke care and policy align? Neurology. 2019 Feb 26;92(9):427-434. doi: 10.1212/WNL.0000000000006921. Epub 2019 Jan 11.
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Halladay J, Bushnell C, Psioda M, Jones S, Lycan S, Condon C, Xenakis J, Prvu-Bettger J; COMPASS Investigative Team. Patient Factors Associated With Attendance at a Comprehensive Postacute Stroke Visit: Insight From the Vanguard Site. Arch Rehabil Res Clin Transl. 2019 Dec 21;2(1):100037. doi: 10.1016/j.arrct.2019.100037. eCollection 2020 Mar.
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Gesell SB, Halladay JR, Mettam LH, Sissine ME, Staplefoote-Boynton BL, Duncan PW. Using REDCap to track stakeholder engagement: A time-saving tool for PCORI-funded studies. J Clin Transl Sci. 2020 Feb 6;4(2):108-114. doi: 10.1017/cts.2019.444. eCollection 2020 Apr.
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Lutz BJ, Reimold AE, Coleman SW, Guzik AK, Russell LP, Radman MD, Johnson AM, Duncan PW, Bushnell CD, Rosamond WD, Gesell SB. Implementation of a Transitional Care Model for Stroke: Perspectives From Frontline Clinicians, Administrators, and COMPASS-TC Implementation Staff. Gerontologist. 2020 Aug 14;60(6):1071-1084. doi: 10.1093/geront/gnaa029.
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Gesell SB, Coleman SW, Mettam LH, Johnson AM, Sissine ME, Duncan PW. How engagement of a diverse set of stakeholders shaped the design, implementation, and dissemination of a multicenter pragmatic trial of stroke transitional care: The COMPASS study. J Clin Transl Sci. 2020 Nov 5;5(1):e60. doi: 10.1017/cts.2020.552.
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Pastva AM, Coyle PC, Coleman SW, Radman MD, Taylor KM, Jones SB, Bushnell CD, Rosamond WD, Johnson AM, Duncan PW, Freburger JK; COMPASS Investigative Team. Movement Matters, and So Does Context: Lessons Learned From Multisite Implementation of the Movement Matters Activity Program for Stroke in the Comprehensive Postacute Stroke Services Study. Arch Phys Med Rehabil. 2021 Mar;102(3):532-542. doi: 10.1016/j.apmr.2020.09.386. Epub 2020 Oct 22.
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Duncan PW, Bushnell C, Sissine M, Coleman S, Lutz BJ, Johnson AM, Radman M, Pvru Bettger J, Zorowitz RD, Stein J. Comprehensive Stroke Care and Outcomes: Time for a Paradigm Shift. Stroke. 2021 Jan;52(1):385-393. doi: 10.1161/STROKEAHA.120.029678. Epub 2020 Dec 22.
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Bayliss WS, Bushnell CD, Halladay JR, Duncan PW, Freburger JK, Kucharska-Newton AM, Trogdon JG. The Cost of Implementing and Sustaining the COMprehensive Post-Acute Stroke Services Model. Med Care. 2021 Feb 1;59(2):163-168. doi: 10.1097/MLR.0000000000001462.
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Gesell SB, Bushnell CD, Jones SB, Coleman SW, Levy SM, Xenakis JG, Lutz BJ, Bettger JP, Freburger J, Halladay JR, Johnson AM, Kucharska-Newton AM, Mettam LH, Pastva AM, Psioda MA, Radman MD, Rosamond WD, Sissine ME, Halls J, Duncan PW. Implementation of a billable transitional care model for stroke patients: the COMPASS study. BMC Health Serv Res. 2019 Dec 19;19(1):978. doi: 10.1186/s12913-019-4771-0.
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Duncan PW, Bushnell CD, Jones SB, Psioda MA, Gesell SB, D'Agostino RB Jr, Sissine ME, Coleman SW, Johnson AM, Barton-Percival BF, Prvu-Bettger J, Calhoun AG, Cummings DM, Freburger JK, Halladay JR, Kucharska-Newton AM, Lundy-Lamm G, Lutz BJ, Mettam LH, Pastva AM, Xenakis JG, Ambrosius WT, Radman MD, Vetter B, Rosamond WD; COMPASS Site Investigators and Teams.. Randomized Pragmatic Trial of Stroke Transitional Care: The COMPASS Study. Circ Cardiovasc Qual Outcomes. 2020 Jun;13(6):e006285. doi: 10.1161/CIRCOUTCOMES.119.006285. Epub 2020 Jun 1.
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34730000
Citation
Bushnell CD, Kucharska-Newton AM, Jones SB, Psioda MA, Johnson AM, Daras LC, Halladay JR, Prvu Bettger J, Freburger JK, Gesell SB, Coleman SW, Sissine ME, Wen F, Hunt GP, Rosamond WD, Duncan PW. Hospital Readmissions and Mortality Among Fee-for-Service Medicare Patients With Minor Stroke or Transient Ischemic Attack: Findings From the COMPASS Cluster-Randomized Pragmatic Trial. J Am Heart Assoc. 2021 Dec 7;10(23):e023394. doi: 10.1161/JAHA.121.023394. Epub 2021 Nov 3.
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34657341
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Rosamond WD, Kucharska-Newton AM, Jones SB, Psioda MA, Lutz BJ, Johnson AM, Coleman SW, Schilsky SR, Patel MD, Duncan PW. Emergency department utilization after hospitalization discharge for acute stroke: The COMprehensive Post-Acute Stroke Services (COMPASS) study. Acad Emerg Med. 2022 Mar;29(3):369-371. doi: 10.1111/acem.14401. Epub 2021 Nov 1. No abstract available.
Results Reference
derived
Links:
URL
https://www.nccompass-study.org/
Description
COMPASS Study website
Available IPD and Supporting Information:
Available IPD/Information Type
Full Data Package
Available IPD/Information URL
https://www.pcori.org/about-us/governance/policy-data-management-and-data-sharing
Learn more about this trial
Comprehensive Post-Acute Stroke Services
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