Ignite Creation Date:
2024-05-05 @ 11:23 AM
Last Modification Date:
2024-10-26 @ 9:06 AM
Study NCT ID:
NCT00011583
Status:
COMPLETED
Last Update Posted:
2008-03-11
First Post:
2001-02-22
Brief Title:
Robot Assisted Upper Limb Neuro-Rehabilitation
Sponsor:
US Department of Veterans Affairs
Organization:
VA Office of Research and Development
Study Overview
Official Title:
Robot Assisted Upper Limb Neuro-Rehabilitation
Status:
COMPLETED
Status Verified Date:
2008-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Our long term objectives are to understand the mechanisms of motor impairment following neurologic injury and to develop interventions to improve motor recovery A series of complementary overlapping clinical trials and development activities will validate and optimize the use of robot-assisted upper limb therapy for neuro rehabilitation
We have developed a robotic system that assists or resists elbow and shoulder movements in three dimensional space In addition to unilateral exercise modes a novel bimanual mode enables hemiparetic subjects to practice mirror image upper limb exercises
We have developed a robotic system that assists or resists elbow and shoulder movements in three dimensional space In addition to unilateral exercise modes a novel bimanual mode enables hemiparetic subjects to practice mirror image upper limb exercises
Detailed Description:
Randomized controlled clinical trial of the Mirror Image Movement Enabler MIME robotic device for shoulder and elbow neurorehabilitation in subacute stroke patients MIME incorporates a PUMA 560 robot that applies forces to the paretic limb during unilateral and bilateral movements in three dimensions Robot-assisted treatment bilateral unilateral and combined bilateral and unilateral was compared with conventional therapy
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