NCT00396708

Wearable Robotic Functional Assistance for Stroke Rehabilitation

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 20 (estimated)
• Sponsor: Myomo · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This study aims to evaluate the effectiveness of using the myomo e100 wearable robotic rehabilitation system for increasing functional independence and long term rehabilitation of chronic stroke victims with a hemiparetic upper extremity.

Detailed description

This is a case controlled study for evaluation of the effectiveness of using the myomo e100 wearable robotic rehabilitation for upper arm therapy following stroke. The intervention for the study will be for the control group- 6-8 weeks of therapeutic exercise and functional training for a total of 18 hours of intervention, or the case group- 6-8 weeks of therapeutic exercise and functional training with the use of the AJB for a total of 18 hours of intervention. Each session will be one hour in length. The length of the study and length of each session is per standard rehabilitation protocol that has been well documented in previous studies as well as the pilot study regarding the AJB. A pre and post test with a 3 month follow up of all measures will be included in the study. Study procedures will focus on performing functional tasks using the e100.

Conditions

• CVA (Cerebrovascular Accident)

Interventions

Type	Name	Description
DEVICE	myomo e100 neurorobotic elbow brace

Timeline

• Start date: 2006-08-01
• Primary completion: 2007-12-01
• First posted: 2006-11-07
• Last updated: 2010-02-03

Locations

1 site across 1 country: United States