Ignite Creation Date:
2024-05-06 @ 2:06 AM
Last Modification Date:
2024-10-26 @ 11:14 AM
Study NCT ID:
NCT01974635
Status:
TERMINATED
Last Update Posted:
2019-06-13
First Post:
2013-10-21
Brief Title:
Proprioception Testing in Persons With Sensorimotor Impairment
Sponsor:
Oregon Health and Science University
Organization:
Oregon Health and Science University
Study Overview
Official Title:
Proprioception Testing in Persons With Sensorimotor Impairment
Status:
TERMINATED
Status Verified Date:
2019-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Device used for eye-blinks did not work as performed
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
Detailed Description:
The AMES device performs tests of sensorimotor impairment as well as delivering therapy In this study we are testing 2 additional diagnostic tests ie 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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None