Actively Recruiting
Compass 3: A Novel Transition Program to Reduce Disability After Stroke
Led by Washington University School of Medicine · Updated on 2026-02-13
520
Participants Needed
2
Research Sites
234 weeks
Total Duration
On this page
Sponsors
W
Washington University School of Medicine
Lead Sponsor
E
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study evaluates a program designed to help individuals transition from inpatient rehabilitation to home following an ischemic or hemorrhagic stroke. Half of the participants will receive a stroke education program while the other half will receive an environmental modifications program.
CONDITIONS
Official Title
Compass 3: A Novel Transition Program to Reduce Disability After Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 6553 years at the time of screening
- Acute stroke diagnosis (ischemic stroke or intracerebral hemorrhage) confirmed by medical team or records
- Independent in daily activities before the stroke (premorbid Modified Rankin Scale score 6542)
- Planning to be discharged to home from inpatient rehabilitation
- Able to give informed consent and comply with study requirements and duration
You will not qualify if you...
- Life expectancy less than 6 months
- Cognitive impairment that affects ability to provide informed consent or complete self-rated scales
- Communication problems preventing study completion
- Living in a congregate living facility
- Not eligible for a therapeutic pass
- Living outside designated catchment area
- Investigator's judgment that participant cannot complete study procedures or interventions
- Participation in another study that could interfere with this study's assessments or interventions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
University of Missouri
Columbia, Missouri, United States, 65211
Not Yet Recruiting
2
Washington University in St. Louis
St Louis, Missouri, United States, 63110
Actively Recruiting
Research Team
S
Susan Stark, PhD
CONTACT
B
Brianna Holden, OTR/L
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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