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Proprioception Testing in Persons With Sensorimotor Impairment

Stroke Clinical Trial

Official title:
Proprioception Testing in Persons With Sensorimotor Impairment

Clinical Trial Summary

In this study, an FDA-cleared device and type of treatment called "AMES," which stands for Assisted Movement with Enhanced Sensation, will be used to determine whether sensation in the upper limb of individuals with incomplete spinal cord injuries, acquired brain injury, or stroke improves along with movement through treatment. We hypothesize that measureable improvement in the sensation of the upper limb will precede improvement in functional movement.

Clinical Trial Description

The AMES device performs tests of sensorimotor impairment as well as delivering therapy. In this study, we are testing 2 additional diagnostic tests (i.e., Joint Position Test and "Frisbee" Test), both of proprioception, in order to determine which of the two is the best test of proprioception. Our hypotheses are: (1) both sensation and movement recover with AMES treatment, (2) sensory recovery precedes that of movement, (3) robotic delivery of the Joint Position Test produces more reliable test results than does manual delivery of this test, and (4) the Frisbee Test results will parallel those of the Joint Position Test. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01974635
Study type Interventional
Source Oregon Health and Science University
Contact
Status Terminated
Phase N/A
Start date October 2013
Completion date April 2015
View Details
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