Post-Stroke Sensory Reweighting on Walking and Balance Outcomes (NCT06727097)
Tracking the Development and Influence of Post-Stroke Sensory Reweighting on Walking and Balance Outcomes
🩺 Plain-English Summary (8th-Grade Level)
The primary objective of this proof-of-concept study is to longitudinally track the development of post-stroke sensory reweighting (PSR), identify associated structural neuroanatomical correlates, and investigate their relationship to walking and fall outcomes.
Who can join: Review the eligibility criteria below.
Location: University of Cincinnati College of Medicine — Cincinnati, Ohio
Age range: 18 Years
🧪 Interventions in This Study
- Posturography (DIAGNOSTIC_TEST)
- Walking Speed (DIAGNOSTIC_TEST)
- Instrumented 7M Timed UP and GO (DIAGNOSTIC_TEST)
- Fall Event Records (OTHER)
- MRI (3T) (DIAGNOSTIC_TEST)
📋 "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)
- University of Cincinnati College of Medicine — Cincinnati, Ohio
📞 Contact the Study Coordinator
Phone: (513) 558-2919
Email: awosikoe@ucmail.uc.edu
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 Ischemic Stroke
- OsciPulse D-dimer Pilot Trial — Philadelphia, Pennsylvania
- Memantine for Enhanced Stroke Recovery — Salt Lake City, Utah
- Sleep for Stroke Management and Recovery Trial — Birmingham, Alabama
- Left Atrial Appendage Exclusion for Prophylactic Stroke Reduction Trial — Huntsville, Alabama
- A Safety and Tolerability Study of Neural Stem Cells (NR1) in Subjects With Chronic Ischemic Subcortical Stroke (ISS) — Stanford, California
- VNS-REHAB At-Home - Post-Market Study for Using the Vivistim System® at Home — Chicago, Illinois
Explore by condition: All Ischemic Stroke 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.