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Towards MY smart and intuitive controlled LEG prosthesis

Conditions
transfemoral amputation, leg prosthesis, intuitive control, EMG, intention detectiontranfemorale amputatie, beenprothese, intuïtieve controle, EMG, intentie detectie
Registration Number
NL-OMON27197
Lead Sponsor
Roessingh Research and Development
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other
Sex
Not specified
Target Recruitment
70
Inclusion Criteria

Individuals without an amputation

In order to be eligible to participate in this study, a subject must meet all of the following criteria:

Exclusion Criteria

Individuals without an amputation:

A potential subject who meets any of the following criteria will be excluded from participation in this study:

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary study parameter is the misclassification rate of a classifier.<br /><br>The misclassification rate of the classifier that is based on biplor EMG and HD-EMG will be compared. In addition,<br>misclassification rates of classifiers developed with different techniques will also be compared.
Secondary Outcome Measures
NameTimeMethod
Secundary study parameters are:<br /><br>- The misclassification rate for unsupervised algorithms. Unsupervised algorithms will also be compared to supervised<br>algorithms. To determine the effect of repeated measurements on the robustness of the classifier.<br /><br>- The effect of additional sensor information on misclassification rate by using the raw IMU sensor data from the Xsens suit. This information is recorded during measurements anyway, as Xsens uses this information in their biomechanical model to<br>reconstruct movements.
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