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RECRUITINGINTERVENTIONAL

Tracking Post-stroke Walking Improvements From the Clinic Into the Home

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The purpose of this proposal is to use novel video-based movement tracking technology to measure gait quality after stroke - in the home. Current rehabilitation practice assesses walking in the highly controlled 'ideal' clinical environment. The implicit assumption by clinicians and researchers is that the way people walk in the clinic (their best capacity) reflects the way they walk in the real-world (true performance). With advances in computer vision and development of pose estimation algorithms, it is now possible to directly measure how people are walking in their homes. It is critical that researchers apply this technology to examine the basic assumptions that underlie current rehabilitation practice. Here, a video-based pose estimation workflow will be used to 1) contrast the gait patterns of persons post-stroke as observed in-clinical vs. in-home settings, and 2) map the rate of deterioration of clinically-derived walking improvements, in the home. This methodology has been used to accurately measure gait kinematics in people with stroke as they walk in laboratory, however this study now seeks to use these methods to record people with stroke as they walk in their natural home environments. The ultimate outcome of this project will not only be freely-available video-based workflow modified for home-based gait assessments, but also preliminary data revealing how people with stroke walk in the real world.

Who May Be Eligible (Plain English)

Who May Qualify: - stroke \>6 months prior - hemiparetic gait pattern with step length difference of 4cm or greater - able to ambulate whiteout physical assistance from another person (use of an assistive device are acceptable), gait speed \>/= 0.2m/s - normal or corrected-to-normal vision Who Should NOT Join This Trial: - neurological condition other than stroke - aphasia limiting comprehension of task instructions pregnancy - uncontrolled hypertension (\> 150/90 mmHg at rest) - dementia, cognitive impairments, or psychiatric disorders limiting the ability to provide willing to sign a consent form - epilepsy - orthopedic or pain conditions limiting walking - concurrent engagement in physical therapy or other research study. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * stroke \>6 months prior * hemiparetic gait pattern with step length difference of 4cm or greater * able to ambulate whiteout physical assistance from another person (use of an assistive device are acceptable), gait speed \>/= 0.2m/s * normal or corrected-to-normal vision Exclusion Criteria: * neurological condition other than stroke * aphasia limiting comprehension of task instructions pregnancy * uncontrolled hypertension (\> 150/90 mmHg at rest) * dementia, cognitive impairments, or psychiatric disorders limiting the ability to provide informed consent * epilepsy * orthopedic or pain conditions limiting walking * concurrent engagement in physical therapy or other research study.

Treatments Being Tested

BEHAVIORAL

Step length asymmetry training

Participants will engage in four, five-minute periods of step symmetry training during session 2. This training uses established sensorimotor adaptation-based methods (e.g. split-belt treadmill walking, walking with unilateral leg weighting) to elicit motor aftereffects of more equal step lengths. Two minute sitting rest breaks will be given between training blocks or at the participant's request. A video recording will be taken of the first and final two minutes of training.

Locations (1)

Western University of Health Sciences
Lebanon, Oregon, United States