Transitional Care Program to Improve Risk Factors in Stroke Survivors (NCT06657235)
Improved Risk Factor Control Through a Transitional Care Program for Stroke Survivors
🩺 Plain-English Summary (8th-Grade Level)
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
Who can join: Review the eligibility criteria below.
Location: Valley Health System — Winchester, Virginia
Age range: 30 Years
🧪 Interventions in This Study
- Transitional Care Program (OTHER)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Valley Health System — Winchester, Virginia
📞 Contact the Study Coordinator
Phone: (434) 202-3450
Email: admin@syntrillo.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Stroke, Ischemic
- Determinants of the Effectiveness of Robot-assisted Hand Movement Training — Irvine, California
- Visual Rehabilitation After Occipital Stroke — Rochester, New York
- Pathophysiology and Risk of Atrial Fibrillation Detected After Ischemic Stroke — London, Ontario
- The REACTplusNMES Trial: A Double-blinded RCT — Chicago, Illinois
- DELTA (Detecting and Predicting Atrial Fibrillation in Post-Stroke Patients) — Atlanta, Georgia
Explore by condition: All Stroke, Ischemic clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.