Actively Recruiting
Locomotor Recovery and Compensation Post-stroke (LRC)
Led by Indiana University · Updated on 2026-03-05
150
Participants Needed
1
Research Sites
338 weeks
Total Duration
On this page
Sponsors
I
Indiana University
Lead Sponsor
R
Rehabilitation Hospital of Indiana
Collaborating Sponsor
AI-Summary
What this Trial Is About
The proposed research will characterize of the time course of neurological and locomotor recovery as well as development of compensatory strategies throughout sub-acute and chronic phases post stroke. In addition, we will also investigate the extent to which measures of recovery and compensation are malleable and can be altered with specific interventions in both the early and late stages post-stroke. Delineation of the time course of development and magnitude of patterns of recovery and compensation should result in alternative predictive "rules' regarding how patients early post-stroke could recovery functional and neurological function.
CONDITIONS
Official Title
Locomotor Recovery and Compensation Post-stroke (LRC)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals early post-stroke (less than 15-30 days)
- First ever stroke
- Unilateral hemiparesis (weakness on one side)
- Currently receiving inpatient rehabilitation
- Ability to follow one-step commands
- Provision of informed consent
- Medical clearance from rehabilitation physician to participate
You will not qualify if you...
- Uncontrolled cardiovascular, metabolic, or respiratory disease limiting exercise participation (e.g., congestive heart failure, resting blood pressure > 200/110 mmHg, uncontrolled diabetes, end-stage renal disease)
- Absolute criteria for stopping exercise testing during initial or repeated ECG tests according to ACSM guidelines
- Other orthopedic or neurological disorders limiting walking before the stroke
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Rehabilitation Hospital of Indiana
Indianapolis, Indiana, United States, 46254
Actively Recruiting
Research Team
T
Thomas G Hornby
CONTACT
C
Chris Henderson
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
TREATMENT
Number of Arms
2
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