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Clinical Trials in the USA / NCT07222085
Recruiting Not applicable

Long-Term Stability of the Glide Control Strategy

NCT07222085 · tracked via the Priya Life Science USA tracker
Sponsor
Infinite Biomedical Technologies
Phase
Not applicable
Started
2025-10-15
Last updated
2025-11-05

Condition(s) studied

Upper Limb Amputation Above ElbowUpper Limb Amputation Below Elbow

Investigational drug(s) / intervention(s)

Glide Control SystemPattern Recognition System

Glide Control System: Glide is a commercially developed directional myoelectric control strategy from Infinite Biomedical Technologies (IBT) that sits between classic Direct Control (DC) and modern Pattern Recognition (PR). Instead of requiring an isolated on/off muscle signal for each function (e.g., DC) or training a complex classifier on many gestures (e.g., PR), Glide uses the relative activity across 2-8 EMG electrodes to move a virtual cursor on a 2-D "Glide map." The map is divided into adjustable sectors ("slices"), and each slice is assigned a prosthetic movement (e.g., hand open/close, wrist rotation, elbow flexion). Moving the cursor into a slice actuates that movement.

Pattern Recognition System: Pattern recognition (PR)-based myoelectric control is a data-driven approach that allows a user to control multiple prosthetic functions using natural muscle activation patterns rather than discrete, isolated signals. Instead of mapping one muscle to one motion (as in conventional Direct Control), PR systems record the spatial and temporal pattern of EMG activity from multiple sites on the residual limb and use machine learning algorithms to classify which intended movement the user is trying to make.

Study summary

This research is intended to test whether the prescription of the Glide prosthesis control system reduces the burden of use for both patients and their clinical care team as compared to use of Pattern Recognition-based advanced myoelectric control. The goal of the study is to fill the gaps in clinically relevant knowledge to inform the prescription of prosthesis components and the rehabilitation process.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Unilateral trans-radial or trans-humeral limb loss with a healed residual limb * Candidate for 2+ degree-of-freedom (DOF) myoelectric prosthesis as determined by the study prosthetist * Age of 18 years or greater Exclusion Criteria: * Prior experience with Pattern Recognition or Glide control * Individuals with a residual limb that is unhealed from the amputation surgery * Individuals with easily damaged or sensitive skin who would not tolerate EMG electrodes * Significant cognitive deficits as determined upon clinical evaluation * Significant neurological deficits as determined upon clinical evaluation * Significant physical deficits of the residual limb impacting full participation in the study as determined upon clinical evaluation * Uncontrolled pain or phantom pain impacting full participation in the study as determined upon clinical evaluation * Serious uncontrolled medical problems

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
Medical Center Orthotics and Prosthetics - Annapolis Annapolis Maryland Recruiting
Medical Center Orthotics and Prosthetics - Baltimore Baltimore Maryland Recruiting
Medical Center Orthotics and Prosthetics - Silver Spring Silver Spring Maryland Recruiting
Medical Center Orthotics and Prosthetics - Allston Allston Massachusetts Recruiting
Medical Center Orthotics and Prosthetics - Milton Milton Massachusetts Recruiting
Medical Center Orthotics and Prosthetics - Charlotte Charlotte North Carolina Recruiting
Medical Center Orthotics and Prosthetics - Anderson Anderson South Carolina Recruiting
Medical Center Orthotics and Prosthetics - Greenville Greenville South Carolina Recruiting
Medical Center Orthotics and Prosthetics - Fairfax Fairfax Virginia Recruiting
Medical Center Orthotics and Prosthetics - Leesburg Leesburg Virginia Recruiting

More Infinite Biomedical Technologies trials in the USA

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07222085 on ClinicalTrials.gov ↗ ← All trials in the USA