MedPath

Improving Myoelectric Prosthetic and Orthotic Limb Control

Not Applicable
Recruiting
Conditions
Hemiparesis
Interventions
Other: commercially available control algorithm
Other: experimental control algorithm
Registration Number
NCT05509101
Lead Sponsor
University of Utah
Brief Summary

The purpose of this study is to improve control of myoelectrically-controlled advanced orthotic devices (an exoskeleton device that use the body's muscle signals to drive movements of a robotic brace) by using advanced predictive decode algorithms, and the use of high count (\> 8) surface electromyographic (sEMG) electrodes.

Detailed Description

This study looks to improve control of myoelectrically-controlled advanced powered orthoses (orthoses that use the body's muscle signals to drive movements of a robotic exoskeleton) by using advanced predictive decode algorithms, and the use of high count (\> 8) surface electromyographic (sEMG) electrodes.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
45
Inclusion Criteria
  • First-ever ischemic or hemorrhagic stroke
  • Chronic Stroke (at least 6 months since onset)
  • Chronic hemiparesis
  • Functional range of motion for contralateral arm
Exclusion Criteria
  • Individuals who are currently Incarcerated

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Clinically Available Control Algorithm (MyoPro)commercially available control algorithmBinary control of the orthosis is based on a clinically available control algorithm. This condition serves as a control. Participants will use a commercially available device, the MyoPro.
High-Density EMG Control Algorithmexperimental control algorithmControl of the orthosis is based on residual muscle activity mapped to intended movement using advanced predicted algorithms. This condition is a novel algorithm and serves as the experimental condition.
Primary Outcome Measures
NameTimeMethod
Box and Blocks Test (BBT)while using the device (up to 2 hours)

The Box and Blocks test is performed using the orthotic device under each condition. The individual puts on the device for a maximum of two hours. During that time wearing the device, they will use two different algorithms for controlling the device to complete the Box and Blocks Test.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Utah

🇺🇸

Salt Lake City, Utah, United States

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