NCT06657235Recruiting
Transitional Care Program to Improve Risk Factors in Stroke Survivors
Improved Risk Factor Control Through a Transitional Care Program for Stroke Survivors
Source: ClinicalTrials.gov · Last updated 3 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 224 (estimated)
- First submitted
- 15 Oct 2024
- Start date
- 16 Aug 2024
- Primary completion date
- Dec 2025
- Lead sponsor
- Syntrillo, Inc
- Diseases
- Stroke
- NCT number
- NCT06657235
What you commit to
- Study type: Interventional
- Planned participants: 224
- From 16 Aug 2024 to the primary completion date, Dec 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- 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 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.
Other
- 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 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.
Who the study is looking for
- 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
Age in the registry: 30 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Valley Health System Coordinator of this site? Confirm its status | Winchester | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.