45 Participants Needed

Sensory Reweighting for Stroke

(PSR Trial)

CD
oA
Overseen Byoluwole Awosika, MD, MSCR
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Cincinnati
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores how individuals who have had a stroke adjust their senses, such as balance and movement, and how these changes affect their ability to walk and avoid falls. Researchers focus on individuals who have experienced their first ischemic stroke, caused by a blockage in the brain, on one side. The study aims to identify brain changes that occur after a stroke and how these changes impact recovery in walking and balance. Individuals who have had a single-sided ischemic stroke and can consent to participate while still in the hospital may be a good fit. As an unphased trial, this study offers a unique opportunity to contribute to understanding stroke recovery and improving future treatments.

Why are researchers excited about this trial?

Researchers are excited about the trial on sensory reweighting for stroke survivors because it explores a new approach to improving walking and balance. Unlike traditional rehabilitation options that focus primarily on repetitive physical exercises, this method targets the brain's ability to adapt how it processes sensory information. This could potentially lead to more effective and faster recovery of motor functions by helping the brain compensate for deficits caused by the stroke. Such innovative techniques could redefine stroke rehabilitation by enhancing the brain's natural plasticity, offering hope for better and quicker outcomes.

Who Is on the Research Team?

OA

Oluwole Awosika, MD, MSCR

Principal Investigator

University of

Are You a Good Fit for This Trial?

Inclusion Criteria

I have had my first stroke.
I have had a stroke caused by a lack of blood flow.
I can give my own consent before leaving the hospital.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants undergo neurorehabilitation interventions and assessments for post-stroke sensory reweighting

6 months
Regular assessments at 2, 4, and 6 months post-stroke

Follow-up

Participants are monitored for walking and balance outcomes, including fall events

6 months
Assessments at 2, 4, and 6 months post-stroke

What Are the Treatments Tested in This Trial?

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Stroke SurvivorsExperimental Treatment5 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Cincinnati

Lead Sponsor

Trials
442
Recruited
639,000+

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator

Trials
2,103
Recruited
2,760,000+