Transitional Care Program to Improve Risk Factors in Stroke Survivors

Part of paid clinical trials in Winchester, Virginia.

Sponsor
Syntrillo, Inc
Study ID
NCT06657235
Status
Recruiting
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Conditions

  • Stroke, Ischemic

Eligibility Criteria

Sex
ALL
Age
30 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Transitional Care Program — OTHER
    Participants will receive personalized risk-factor management stroke care from a multidisciplinary team trained by our neurologists to understand the needs of stroke survivors and the nuances of stroke care. Risk factor data from in-home devices, health records, and self-reports will be collected along with functional status and behavioral data obtained through validated questionnaires and an occupational therapy evaluation. Syntrillo's neurology provider will review this data, assess the participant through a telemedicine encounter, and create a comprehensive secondary prevention plan to supplement the participant's care plan at discharge. Data generated through these clinical encounters will be de-identified and used for subsequent development of Syntrillo's stroke management technology.

Study Details

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

Key Dates

Start date
Aug 16, 2024
Status verified
May 2025
Primary completion
Dec 31, 2025
Completion
Dec 31, 2025

Study Design

Enrollment
224 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH

Arms

  • Experimental: Early Enrollment
    Participants enrolled around the time of discharge from the hospital immediately following an ischemic stroke.
  • Experimental: Late Enrollment
    Participants enrolled mainly between 3-5 months after their discharge from the hospital following an ischemic stroke.

Primary Outcome Measure

Increased compliance with therapeutic standards of care according to the American Heart Association (AHA) guidelines for secondary stroke prevention in early vs late group [ Time Frame: From enrollment to the end of the 6 month monitoring period ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Valley Health SystemWinchesterVirginia22601-

Find similar trials in Winchester, VA

By research site
Valley Health System· Winchester, VA

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