A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy

A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy

Citation Author(s):
Ronald
Bos
Delft University of Technology
Kostas
Nizamis
University of Twente
Bart
Koopman
University of Twente
Just
Herder
Delft University of Technology
Massimo
Sartori
University of Twente
Dick
Plettenburg
Delft University of Technology
Submitted by:
Kostas Nizamis
Last updated:
Wed, 03/13/2019 - 11:40
DOI:
10.21227/gerz-8s29
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Abstract: 

The dataset, includes raw data, observations and biometric data from our case study with an individual with DMD, controlling for the first time an active hand orthosis.

Instructions: 

The dataset includes 3 files. 

 

The file entitled: 20181022 - DMD exp notes, includes direct feedback we received from the participant without explicitely asking. 

It contains notes and observations of events that happened during the experiment.

 

The file entitled: 20181022 - DMD participant Force and sEMG Raw Data, has 5 tabs. The first tab includes all the sEMG related raw data from the participant.

The second tab has all the Force related raw data from the participant. The third tab has the maximal values of force and sEMG achieved by the participant.

The fourth tab has the times (expressed in sample), that each trial started. In order to segment the raw data, based on each trial, use these times and add 13499samples (13500 samples or 13.5 seconds is the total duration of each trial).

The fifth tab has the metadata (units, sampling times etc.)

 

The file entitled: 20181022 - DMD participant info, includes the biometric data from the participant.

 

Dataset Files

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[1] Ronald Bos, Kostas Nizamis, Bart Koopman, Just Herder, Massimo Sartori, Dick Plettenburg, "A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy", IEEE Dataport, 2019. [Online]. Available: http://dx.doi.org/10.21227/gerz-8s29. Accessed: May. 20, 2019.
@data{gerz-8s29-19,
doi = {10.21227/gerz-8s29},
url = {http://dx.doi.org/10.21227/gerz-8s29},
author = {Ronald Bos; Kostas Nizamis; Bart Koopman; Just Herder; Massimo Sartori; Dick Plettenburg },
publisher = {IEEE Dataport},
title = {A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy},
year = {2019} }
TY - DATA
T1 - A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy
AU - Ronald Bos; Kostas Nizamis; Bart Koopman; Just Herder; Massimo Sartori; Dick Plettenburg
PY - 2019
PB - IEEE Dataport
UR - 10.21227/gerz-8s29
ER -
Ronald Bos, Kostas Nizamis, Bart Koopman, Just Herder, Massimo Sartori, Dick Plettenburg. (2019). A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy. IEEE Dataport. http://dx.doi.org/10.21227/gerz-8s29
Ronald Bos, Kostas Nizamis, Bart Koopman, Just Herder, Massimo Sartori, Dick Plettenburg, 2019. A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy. Available at: http://dx.doi.org/10.21227/gerz-8s29.
Ronald Bos, Kostas Nizamis, Bart Koopman, Just Herder, Massimo Sartori, Dick Plettenburg. (2019). "A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy." Web.
1. Ronald Bos, Kostas Nizamis, Bart Koopman, Just Herder, Massimo Sartori, Dick Plettenburg. A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy [Internet]. IEEE Dataport; 2019. Available from : http://dx.doi.org/10.21227/gerz-8s29
Ronald Bos, Kostas Nizamis, Bart Koopman, Just Herder, Massimo Sartori, Dick Plettenburg. "A case study with SymbiHand: an sEMG-controlled electrohydraulic hand orthosis for individuals with Duchenne muscular dystrophy." doi: 10.21227/gerz-8s29