πŸ›οΈ Verified NIH Record β€’ Updated 2026-03-31

Optimizing Gait Symmetry After Stroke Using Mechanical Constraints and Sensory Feedback (NCT07087769)

Optimizing Post-Stroke Gait Symmetry: Integrating Mechanical Constraints and Sensory Feedback to Enhance Paretic Leg Propulsion

🟒 Recruiting Observational / Diagnostic 🧠 Behavioral & Psychological Program Sponsor: The University of Texas Medical Branch, Galveston

🩺 Plain-English Summary (8th-Grade Level)

This single-session study aims to evaluate a novel gait training protocol that integrates mechanical constraints and sensory feedback to enhance paretic leg propulsion in individuals post-stroke. The study will include 15 individuals who have experienced a stroke and 15 healthy adults, each aged 20 years or older. Participants will walk on both tied-belt and split-belt treadmills under various training conditions, including backward-directed resistance (applied at the pelvis, ankle, or both) and real-time sensory feedback (visual, auditory, or combined). These interventions will be applied individually and in combination to identify the most effective environment for promoting symmetrical gait patterns. Each session will last approximately two hours. The equipment used is non-invasive, and the risk to participants is minimal.

Who can join: Review the eligibility criteria below.

Location: University of Texas Medical Branch β€” Galveston, Texas

Age range: 20 Years

πŸ§ͺ Interventions in This Study

  • Treadmill Walking with Split-Belt and/or Tied-Belt Conditions (BEHAVIORAL)
  • Mechanical Resistance (Pelvis and/or Ankle) depending on participant's walking capacity (BEHAVIORAL)
  • Sensory Feedback Training (BEHAVIORAL)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (1 Sites)

  • University of Texas Medical Branch β€” Galveston, Texas

πŸ“ž Contact the Study Coordinator

Phone: (409) 747-1617

Email: mako@utmb.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° 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 Β§ 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.

Explore by condition: All Stroke clinical trials

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—