Wearable Robotic Functional Assistance for Stroke Rehabilitation
- Conditions
- CVA (Cerebrovascular Accident)
- Registration Number
- NCT00396708
- Lead Sponsor
- Myomo
- Brief 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
- Medically Stable
- Cognitive Awareness
- Weakness in upper arm
- Over 1 year post CVA
- not engaged in any other upper arm therapies
- Rashes, open wounds or skin sensitivity on arm
- Very high elbow tone (arm rigid in flexion or extension)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Motor Activity Log Fugl-Meyer Upper Arm Function Wolf Motor Function SF-36 QOL Survey Range of Motion Muscle Strength Test
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
myomo Inc.
🇺🇸Boston, Massachusetts, United States