Evaluating Error Augmentation for Neurorehabilitation



Status:Completed
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:January 2008
End Date:March 2012

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This is a sub-project of a larger NIDRR Grant. One promising form of robotic training that
leverages the power of neuro-plasticity is error augmentation. In this paradigm the computer
singles out and magnifies a stroke survivor's movement errors from a desired trajectory,
thus forcing the subjects to strengthen their control. Using the VRROOM, a state-of-the-art
system which uses haptics (robotic forces) and graphics (visual display) interfaces, a
subject's desired trajectory can be determined and the movement errors can be amplified in
real-time with dramatic results. This project evaluates a practical approach of error
augmentation, using therapist-driven trajectories. The investigators intend to determine
clinical efficacy of several types of therapist-assisted error augmentation on retraining
the nervous system in functional activities. The investigators will test two experimental
treatments in a crossover design. The investigators hypothesize that combined haptic and
visual error augmentation will lead to the best functional recovery.


Inclusion Criteria:

- adult (age >18)

- survived a single cortical stroke at least 6 months previously involving ischemia or
hemorrhage of the middle cerebral artery (MCA),

- demonstrated the presence of some active shoulder and elbow movement (characterized
by Fugl-Meyer Assessment Upper Extremity scores ranging from 15-50 for ARM 1; 25-50
for ARM 2).

Exclusion Criteria:

- diffuse or multiple lesion sites or multiple stroke events

- bilateral paresis

- severe spasticity or contracture (Modified Ashworth ≥3

- severe concurrent medical problems

- severe sensory deficits

- cerebellar strokes resulting in severe ataxia

- significant shoulder pain

- focal tone management with Botulinim Toxin (Botox®) injection to the hemiparetic
upper extremity (UE) within the previous four months,

- aphasia that would influence the ability to perform the experiment

- cognitive impairment (Mini Mental State Examination < 23/30)

- affective dysfunction that would influence the ability to perform the experiment

- depth perception impairment (< 3 on Stereo Circle Test)

- visual field cut or hemispatial neglect that would influence the ability to
participate in the activity

- inability to provide informed consent
We found this trial at
1
site
345 E Superior St
Chicago, Illinois 60611
(312) 238-1000
Rehabilitation Institute of Chicago The Rehabilitation Institute of Chicago (RIC) is an independent, 501(c)3, non-profit...
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mi
from
Chicago, IL
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