No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
30 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
224 (estimated)
Sponsor
Syntrillo, Inc · Other
Who this trial is looking for
This trial is looking for people aged 30 or older who have had an ischemic stroke. Participants will track their health information and meet with healthcare providers to help manage their stroke risk factors.
Are You a Good Fit for This Trial?
You may be able to join if
I am 30 years old or older.
I have had an ischemic stroke based on CT or MRI.
My modified Rankin score is 3 or less.
I am being enrolled right after my hospital stay or 3-5 months later.
You may not be able to join if
I have had a hemorrhagic stroke.
I have dementia.
I cannot communicate fluently in English.
I do not have reliable internet access for telemedicine visits.
I am currently enrolled in another clinical study.
I do not live in Virginia, West Virginia, Tennessee, Oklahoma, Illinois, or Michigan.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The goal of this clinical trial is to evaluate whether our transitional care program helps stroke survivors better manage their risk factors for stroke to lower the risk of a repeat stroke. The main question it aims to answer is:
\- Does the program help participants meet the targets set by the American Heart Association clinical guidelines for control of risk factors associated with stroke?
Res…
The goal of this clinical trial is to evaluate whether our transitional care program helps stroke survivors better manage their risk factors for stroke to lower the risk of a repeat stroke. The main question it aims to answer is:
\- Does the program help participants meet the targets set by the American Heart Association clinical guidelines for control of risk factors associated with stroke?
Researchers will compare participants enrolled right after being discharged from the hospital to participants enrolled around 3-5 months after being discharged to examine whether timing differences in enrollment affect the efficacy of the program.
Participants will:
* Keep track of their medications, their exercise, and their health information using smart devices provided by the study
* Answer questions about their health and lifestyle
* Meet with our team of healthcare providers
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria:
All Cohorts:
* Age 30 or above
* Evidence of ischemic stroke documented on CT or MRI
* Modified Rankin score of 3 or less
Early Enrollment:
* Admission for ischemic stroke at a participating site
* Enrolled during their admission for ischemic stroke or within 24 hours of disc…
Inclusion Criteria:
All Cohorts:
* Age 30 or above
* Evidence of ischemic stroke documented on CT or MRI
* Modified Rankin score of 3 or less
Early Enrollment:
* Admission for ischemic stroke at a participating site
* Enrolled during their admission for ischemic stroke or within 24 hours of discharge
Late Enrollment:
* Stroke survivors previously admitted at the participating sites' inpatient stroke unit
* Enrollment date between 1 and 6 months after discharge for inpatient admission for ischemic stroke
Exclusion Criteria:
* Participants determined to have hemorrhagic or periprocedural stroke based on hospital EMR review will be excluded.
* Participants determined to have an ischemic stroke due to dissection based on hospital EMR review will be excluded.
* Participants who lack capacity determined by the care team during their hospitalization (for the early enrollment group) or their most recent clinical encounter (for the late enrollment group) will be excluded.
* Participants with a diagnosis of dementia will be excluded.
* Participants with acute subdural hemorrhage will be excluded.
* Participants with hemorrhagic stroke due to vascular abnormality (aneurysm or AVM) or trauma will be excluded.
* Participants who cannot perform the following will be excluded:
1. offer a consistent choice about participating in the study
2. demonstrate that they can comprehend and recall major features of the study including: participation is voluntary, the major procedures, the primary risk, and the primary benefit.
* Participants who are discharged to Long-term Acute Care Hospitals will be excluded.
* Participants who are unable to read or communicate fluently in English will be excluded.
* Participants who do not have reliable internet access to complete telemedicine visits per self-report will be excluded.
* Participants already enrolled in another clinical study which could impact the frequency of monitoring or care that participant receives.
* Participants who do not reside in Virginia, West Virginia, Tennessee, Oklahoma, Illinois, or Michigan will be excluded.
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