Winchester, VANCT06657235Now EnrollingIRB Ready

Stroke, Ischemic Clinical Trial in Winchester, VA

Access cutting-edge stroke, ischemic treatment through this clinical trial at a research site in Winchester. Study-provided care at no cost to qualified participants.

Sponsored by Syntrillo, Inc

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Expert Care in Winchester

Access stroke, ischemic specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related stroke, ischemic treatment provided free

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Check if you qualify for this stroke, ischemic clinical trial in Winchester, VA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Winchester

    Convenient for VA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Winchester site if eligible
  4. 4Begin participation

About This Stroke, Ischemic Study in Winchester

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

Sponsor: Syntrillo, Inc

Who Can Participate

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:
offer a consistent choice about participating in the study
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.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Winchester?

Yes, this clinical trial (NCT06657235) has an active research site in Winchester, VA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Stroke, Ischemic Treatment Options in Winchester, VA

If you're searching for stroke, ischemic treatment options in Winchester, VA, this clinical trial (NCT06657235) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Winchester research site is actively enrolling participants for this clinical trial. You'll receive care from experienced stroke, ischemic specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all stroke, ischemic clinical trials near you to find additional studies recruiting in your area.

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