RECRUITING

Transitional Care Program to Improve Risk Factors in Stroke Survivors

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

Improved Risk Factor Control Through a Transitional Care Program for Stroke Survivors

Quick Facts

Study Start:2024-08-16
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06657235

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:30 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 30 or above
  2. * Evidence of ischemic stroke documented on CT or MRI
  3. * Modified Rankin score of 3 or less
  4. * Admission for ischemic stroke at a participating site
  5. * Enrolled during their admission for ischemic stroke or within 24 hours of discharge
  6. * Stroke survivors previously admitted at the participating sites' inpatient stroke unit
  7. * Enrollment date between 1 and 6 months after discharge for inpatient admission for ischemic stroke
  1. * Participants determined to have hemorrhagic or periprocedural stroke based on hospital EMR review will be excluded.
  2. * Participants determined to have an ischemic stroke due to dissection based on hospital EMR review will be excluded.
  3. * 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
  4. * Participants with a diagnosis of dementia will be excluded.
  5. * Participants who cannot perform the following will be excluded:
  6. 1. offer a consistent choice about participating in the study
  7. 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.
  8. * Participants who are discharged to Long-term Acute Care Hospitals or Skilled Nursing Facilities because they are unable to meet the minimum threshold for daily rehabilitation therapy for an Acute Rehabilitation Facility will be excluded.
  9. * Participants who are unable to read or communicate fluently in English will be excluded.
  10. * Participants who do not have reliable internet access to complete telemedicine visits per self-report will be excluded.

Contacts and Locations

Study Contact

Andrea M Samayoa-Sosa
CONTACT
434-202-3450
admin@syntrillo.com

Study Locations (Sites)

MaineHealth Maine Medical Center Portland
Portland, Maine, 04102
United States
Sentara Norfolk General Hospital
Norfolk, Virginia, 23510
United States
Valley Health System
Winchester, Virginia, 22601
United States

Collaborators and Investigators

Sponsor: Syntrillo, Inc

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-08-16
Study Completion Date2025-12

Study Record Updates

Study Start Date2024-08-16
Study Completion Date2025-12

Terms related to this study

Keywords Provided by Researchers

  • transitional care program
  • secondary stroke prevention
  • stroke care

Additional Relevant MeSH Terms

  • Stroke, Ischemic