Tracking Sensory Changes and Walking After Stroke
Follows adults with stroke to study how sensory changes relate to walking and falls.
Plain-language title generated from the registry record
Registry title: Post-Stroke Sensory Reweighting on Walking and Balance Outcomes
Key facts
- Where
- Cincinnati, United StatesSee the site
Where in United States
- University of Cincinnati College of MedicineCincinnati, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- University of Cincinnati
- Trial code
- NCT06727097
- Record updated
- 2 September 2026
- Original description
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.Read full original descriptionShow less
Tracking the Development and Influence of Post-Stroke Sensory Reweighting on Walking and Balance Outcomes
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.
Inclusion: First ever clinical stroke; Stroke due to ischemia; Age 18 years or older; Ability to consent by patient (not surrogate), any time prior to acute hospital discharge.
Exclusion: Pre-stroke dependence (modified Rankin Scale score of 3 or more); Isolated brainstem or cerebellar stroke; Low likelihood of survival beyond the acute hospitalization, such as malignant cerebral edema; Pre-existing co-morbid conditions that significantly affects vision, somatosensory function, vestibular system, orthostasis, coordination or mobility; Post stroke mRS>4 or discharge to hospice; Bilateral acute strokes; Co-enrollment in a trial of an intervention through six-month follow-up; Inability to maintain follow-up with study procedures through six-month follow-up; Contraindication to non-contrast MRI.