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NCT06727097Recruiting

Post-Stroke Sensory Reweighting on Walking and Balance Outcomes

Tracking the Development and Influence of Post-Stroke Sensory Reweighting on Walking and Balance Outcomes

Source: ClinicalTrials.gov · Last updated 2 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
45 (estimated)
First submitted
6 Dec 2024
Start date
1 Nov 2024
Primary completion date
31 Jul 2027
Lead sponsor
University of Cincinnati
Diseases
Stroke
NCT number
NCT06727097

What you commit to

  • Study type: Observational
  • Planned participants: 45
  • From 1 Nov 2024 to the primary completion date, 31 Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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

Other

  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Cincinnati College of Medicine
Coordinator of this site? Confirm its status
CincinnatiUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.