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Sub-Acute Stroke Rehabilitation With AMES — AMES  

Cerebrovascular Stroke Clinical Trial

Official title:
Sub-Acute Stroke Rehabilitation With Assisted Movement With Enhanced Sensation

Clinical Trial Summary

The AMES device is designed to produce functional cortical changes by:(1) assisting the subject as he/she attempts to move the limb (assisted movement) and (2) enhancing movement sensation by vibrating the muscles during movement (enhanced sensation). The primary hypothesis is that the combination of assisted movement and enhanced sensation from muscle vibration can increase the amount of motor recovery in individuals disabled by a stroke.

Clinical Trial Description

Approximately 700,000 U.S. citizens have a stroke each year with about half ending up with significant motor disabilities. There are an estimated 5 million stroke survivors in the U.S., making strokes the leading cause of long-term disability in the U.S.. Existing rehabilitation therapies have not been effective in returning all stroke survivors to full motor recovery. The AMES device was designed to be able to provide therapy for the hand (fingers/wrist). In this 18 treatment sessions, double-blinded, control study, AMES therapy will be provided in addition to the usual physician-ordered rehabilitation during the sub-acute period following a stroke. Those control subject who complete the Phase 1 placebo sessions will have the opportunity to cross-over to participate in a AMES treatment group for a Phase 2. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00609115
Study type Interventional
Source AMES Technology
Contact
Status Completed
Phase N/A
Start date September 1, 2007
Completion date February 28, 2011
View Details
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