Compass 3: A Novel Transition Program to Reduce Disability After Stroke
Recruiting now · Not applicable
Conditions studied: Stroke
In brief
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.
Key facts
- Study ID
- NCT07069660
- Run by
- Washington University School of Medicine
- People needed
- 520
- Starts
- 2025-09-29
- Expected to finish
- 2030-03-31
- Last updated by the study team
- 2026-02-13
Who can join
Age: 55 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Aged ≥55 years at the time of screening
- Acute stroke diagnosis (IS or ICH) verified by the stroke team or medical record
- Independent in activities of daily living (ADLs) prior to stroke (premorbid Modified Rankin Scale score ≤2)
- Plan to discharge to home from an IR
- Capable of giving informed consent which includes compliance with the requirements and duration of participation as listed in the Informed Consent Form (ICF).
You may not qualify if…
- Life expectancy <6 months
- Cognitive impairment that the participant's stroke team or a research team member believes impairs their ability to provide informed consent or make reasoned choice including the interpretation of the self-rated scales
- Any communication problem that would prevent study completion
- Residence in a congregate living facility
- Not eligible for a therapeutic pass
- Residence outside of the designated catchment area (specific catchment distance to be determined by each site)
- Site investigator's judgment that the participant would not be able to complete research procedures or interventions
- Participation in another research study that in the site investigator's judgment could interfere or conflict with this research study's assessments or interventions
Where it is running
- Washington University in St. Louis — St Louis, Missouri, United States (enrolling)
- University of Missouri — Columbia, Missouri, United States
Full record on ClinicalTrials.gov
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