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
π©Ί 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
π§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)
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π All Participating Trial Locations (1 Sites)
- University of Texas Medical Branch β Galveston, Texas
π 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.
π° 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.
More studies in Stroke
- Validation of a Spasticity Measurement Tool β Chicago, Illinois
- GaitBetter: Motor and Cognitive Training for Gait Rehabilitation and Falls Prevention in Stroke Survivors. β Boston, Massachusetts
- Determining the Optimal Dose of Reactive Balance Training After Stroke β Toronto, Ontario
- AMPLATZER PFO Occluder Post Approval Study β Birmingham, Alabama
- Reflex Excitability in Post-stroke Stiff-Knee Gait β Cleveland, Ohio
- Group Lifestyle Balanceβ’ for Individuals With Stroke (GLB-CVA) β Dallas, Texas
Explore by condition: All Stroke clinical trials
π‘ 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.