Actively Recruiting
Transitional Care Program to Improve Risk Factors in Stroke Survivors
Led by Syntrillo, Inc · Updated on 2025-06-03
224
Participants Needed
1
Research Sites
67 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Transitional Care Program to Improve Risk Factors in Stroke Survivors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 30 or above
- Evidence of ischemic stroke documented on CT or MRI
- Modified Rankin score of 3 or less
- For early enrollment: admission for ischemic stroke at a participating site and enrolled during admission or within 24 hours of discharge
- For late enrollment: stroke survivors admitted previously at participating sites and enrolled between 1 and 6 months after discharge
You will not qualify if you...
- Hemorrhagic or periprocedural stroke based on hospital records
- Ischemic stroke caused by dissection
- Lack of capacity to consent determined by care team
- Diagnosis of dementia
- Acute subdural hemorrhage
- Hemorrhagic stroke due to vascular abnormality (aneurysm or AVM) or trauma
- Inability to consistently choose participation or comprehend study features
- Discharge to Long-term Acute Care Hospitals
- Inability to read or communicate fluently in English
- No reliable internet access for telemedicine visits
- Enrollment in another clinical study affecting monitoring or care frequency
- Residence outside Virginia, West Virginia, Tennessee, Oklahoma, Illinois, or Michigan
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Valley Health System
Winchester, Virginia, United States, 22601
Actively Recruiting
Research Team
R
Research Coordinator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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