Gait Event Detection and Travel Distance Using Waist-Worn Accelerometers across a Range of Speeds: Automated Approach
Albara Ah Ramli,
No information about this author
Xin Liu,
No information about this author
K Berndt
No information about this author
et al.
Sensors,
Journal Year:
2024,
Volume and Issue:
24(4), P. 1155 - 1155
Published: Feb. 9, 2024
Estimation
of
temporospatial
clinical
features
gait
(CFs),
such
as
step
count
and
length,
duration,
frequency,
speed,
distance
traveled,
is
an
important
component
community-based
mobility
evaluation
using
wearable
accelerometers.
However,
accurate
unsupervised
computerized
measurement
CFs
individuals
with
Duchenne
muscular
dystrophy
(DMD)
who
have
progressive
loss
ambulatory
difficult
due
to
differences
in
patterns
magnitudes
acceleration
across
their
range
attainable
velocities.
This
paper
proposes
a
novel
calibration
method.
It
aims
detect
steps,
estimate
stride
lengths,
determine
travel
distance.
The
approach
involves
combination
observation,
machine-learning-based
detection,
regression-based
length
prediction.
method
demonstrates
high
accuracy
children
DMD
typically
developing
controls
(TDs)
regardless
the
participant’s
level
ability.
Fifteen
fifteen
TDs
underwent
supervised
testing
speeds
10
m
or
25
run/walk
(10
MRW,
MRW),
100
(100
6-min
walk
(6
MWT),
free-walk
(FW)
evaluations
while
wearing
mobile-phone-based
accelerometer
at
waist
near
body’s
center
mass.
Following
by
trained
evaluator,
were
extracted
from
data
multi-step
process
results
compared
ground-truth
observation
data.
Model
predictions
vs.
observed
values
for
counts,
showed
strong
correlation
(Pearson’s
r
=
−0.9929
0.9986,
p
<
0.0001).
estimates
demonstrated
mean
(SD)
percentage
error
1.49%
(7.04%)
1.18%
(9.91%)
0.37%
(7.52%)
observations
combined
6
MWT,
FW
tasks.
Our
study
findings
indicate
that
single
waist-worn
calibrated
individual’s
characteristics
our
methods
accurately
measures
distances
common
both
TD
peers.
Language: Английский
Wearable sensors in paediatric neurology
Developmental Medicine & Child Neurology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 31, 2025
Wearable
sensors
have
the
potential
to
transform
diagnosis,
monitoring,
and
management
of
children
who
neurological
conditions.
Traditional
methods
for
assessing
disorders
rely
on
clinical
scales
subjective
measures.
The
snapshot
disease
progression
at
a
particular
time
point,
lack
cooperation
by
during
assessments,
susceptibility
bias
limit
utility
these
sensors,
which
capture
data
continuously
in
natural
settings,
offer
non-invasive
objective
alternative
traditional
methods.
This
review
examines
role
wearable
various
paediatric
conditions,
including
cerebral
palsy,
epilepsy,
autism
spectrum
disorder,
attention-deficit/hyperactivity
as
well
Rett
syndrome,
Down
Angelman
Prader-Willi
neuromuscular
such
Duchenne
muscular
dystrophy
spinal
atrophy,
ataxia,
Gaucher
disease,
headaches,
sleep
disorders.
highlights
their
application
tracking
motor
function,
seizure
activity,
daily
movement
patterns
gain
insights
into
therapeutic
response.
Although
challenges
related
population
size,
compliance,
ethics,
regulatory
approval
remain,
technology
promises
improve
trials
outcomes
patients
neurology.
Language: Английский
The necessity for skeletal muscle contractile assays to assess treatment efficacy in DMD
Chia-Yi Yuan,
No information about this author
Amanda Sweeten,
No information about this author
Robert W. Grange
No information about this author
et al.
Rare Disease and Orphan Drugs Journal,
Journal Year:
2025,
Volume and Issue:
4(1)
Published: March 3, 2025
Body
movement
relies
on
skeletal
muscles
generating
power
to
move
limbs
effectively.
Power
is
defined
as
force
multiplied
by
velocity:
a
muscle
produces
at
specific
velocity
(the
speed
of
shortening)
and
this
results
in
power.
In
diseases
like
Duchenne
Muscular
Dystrophy
(DMD),
the
absence
dystrophin
weakens
impairs
their
shortening
velocity,
leading
decreased
consequently,
impaired
movement.
Additionally,
diaphragm
heart
are
also
affected
DMD,
causing
difficulty
breathing
cardiac
function.
Compromised
cardiorespiratory
function
can
ultimately
lead
death.
Given
complex
etiology
DMD
essential
role
all
muscles,
it
crucial
assess
potential
treatments
for
effectiveness
improving
This
review
focuses
fundamental
physiological
assays
used
evaluate
muscles.
Common
include
force-frequency,
force-velocity,
power,
eccentric
protocols,
which
conducted
ex
vivo
,
situ
small
rodents
(such
mice
rats)
larger
intermediate
animal
models
such
Golden
Retriever
dog.
Existing
data
support
use
contractile
objective
tools
assessing
efficacy
treatments.
Language: Английский
A Machine-Learning Method of Predicting Vital Capacity Plateau Value for Ventilatory Pump Failure Based on Data Mining
Healthcare,
Journal Year:
2021,
Volume and Issue:
9(10), P. 1306 - 1306
Published: Sept. 30, 2021
Ventilatory
pump
failure
is
a
common
cause
of
death
for
patients
with
neuromuscular
diseases.
The
vital
capacity
plateau
value
(VCPLAT)
an
important
indicator
to
judge
the
status
ventilatory
congenital
myopathy,
Duchenne
muscular
dystrophy
and
spinal
atrophy.
Due
complex
relationship
between
VCPLAT
patient’s
own
condition,
it
difficult
predict
pediatric
disease
from
medical
perspective.
We
established
prediction
model
based
on
data
mining
machine
learning.
first
performed
correlation
analysis
recursive
feature
elimination
cross-validation
(RFECV)
provide
high-quality
combinations.
Based
this,
Light
Gradient
Boosting
Machine
(LightGBM)
algorithm
was
establish
powerful
performance.
Finally,
we
verified
validity
superiority
proposed
method
via
comparison
other
models
in
similar
works.
After
10-fold
cross-validation,
had
best
performance
its
explained
variance
score
(EVS),
mean
absolute
error
(MAE),
squared
(MSE),
root
square
(RMSE),
median
(MedAE)
R2
were
0.949,
0.028,
0.002,
0.045,
0.015
0.948,
respectively.
It
also
well
test
datasets.
Therefore,
can
accurately
effectively
VCPLAT,
thereby
determining
severity
condition
auxiliary
decision-making
doctors
clinical
diagnosis
treatment.
Language: Английский
Population longitudinal analysis of Gait Profile Score and North Star Ambulatory Assessment in children with Duchenne muscular dystrophy
Jiexin Deng,
No information about this author
Fangli Liu,
No information about this author
Zhifen Feng
No information about this author
et al.
CPT Pharmacometrics & Systems Pharmacology,
Journal Year:
2024,
Volume and Issue:
13(5), P. 891 - 903
Published: March 27, 2024
Abstract
Duchenne
muscular
dystrophy
(DMD)
is
a
rare
X‐linked
recessive
disorder
characterized
by
loss‐of‐function
mutations
in
the
gene
encoding
dystrophin.
These
lead
to
progressive
functional
deterioration
including
muscle
weakness,
respiratory
insufficiency,
and
musculoskeletal
deformities.
Three‐dimensional
gait
analysis
(3DGA)
has
been
used
as
tool
analyze
pathology
through
quantification
of
altered
joint
kinematics,
kinetics,
activity
patterns.
Among
3DGA
indices,
Gait
Profile
Score
(GPS),
sensitive
overall
measure
detect
clinically
relevant
changes
patterns
children
with
DMD.
To
enhance
our
understanding
clinical
translation
3DGA,
we
report
here
development
population
nonlinear
mixed‐effect
model
that
jointly
describes
disease
progression
index,
GPS,
endpoint,
North
Star
Ambulatory
Assessment
(NSAA).
The
final
consists
quadratic
structure
for
GPS
linear
GPS‐NSAA
correlation.
Our
was
able
capture
improvement
function
NSAA
younger
subjects,
well
decline
older
subjects.
Furthermore,
predicted
(CFB)
at
1
year
reasonably
DMD
subjects
≤7
years
old
baseline.
tended
slightly
underpredict
after
those
>7
baseline,
but
prediction
summary
statistics
were
maintained
within
standard
deviation
observed
data.
Quantitative
models
such
this
may
help
answer
questions
facilitate
novel
therapies
Language: Английский
Human Pose Estimation for Clinical Analysis of Gait Pathologies
Manal Mostafa Ali,
No information about this author
Maha Medhat Hassan,
No information about this author
Mohamed H. Zaki
No information about this author
et al.
Bioinformatics and Biology Insights,
Journal Year:
2024,
Volume and Issue:
18
Published: Jan. 1, 2024
Gait
analysis
serves
as
a
critical
diagnostic
tool
for
identifying
neurologic
and
musculoskeletal
damage.
Traditional
manual
of
motion
data,
however,
is
labor-intensive
heavily
reliant
on
the
expertise
judgment
therapist.
This
study
introduces
binary
classification
method
quantitative
assessment
gait
impairments,
specifically
focusing
Duchenne
muscular
dystrophy
(DMD),
prevalent
fatal
neuromuscular
genetic
disorder.
The
research
compares
spatiotemporal
sagittal
kinematic
features
derived
from
2D
3D
human
pose
estimation
trajectories
against
concurrently
recorded
capture
(MoCap)
data
healthy
children.
proposed
model
leverages
novel
benchmark
dataset,
collected
YouTube
publicly
available
datasets
their
typically
developed
peers,
to
extract
time-distance
variables
(e.g.
speed,
step
length,
stride
time,
cadence)
joint
angles
lower
extremity
hip,
knee,
knee
flexion
angles).
Machine
learning
deep
techniques
are
employed
discern
patterns
that
can
identify
children
exhibiting
DMD
disturbances.
While
current
capable
distinguishing
between
subjects
those
with
DMD,
it
does
not
differentiate
patients
other
impairments.
Experimental
results
validate
efficacy
our
cost-effective
method,
which
relies
RGB
video,
in
detecting
abnormalities,
achieving
prediction
accuracy
96.2%
Support
Vector
(SVM)
97%
network.
Language: Английский
Digital outcome measures in Duchene muscular dystrophy: Lessons learnt from clinical trials
Journal of Neuromuscular Diseases,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 8, 2024
Duchenne
muscular
dystrophy
is
a
severe
neuromuscular
disorder
characterized
by
progressive
muscle
degeneration
resulting
from
mutations
in
the
dystrophin
gene.
Digital
outcome
measures
offer
promising
alternative
to
traditional
used
clinical
trials.
This
review
explores
development
and
application
of
digital
dystrophy,
emphasizing
feasibility,
reliability,
sensitivity,
validity
these
measures.
The
stride
velocity
95th
centile
has
been
validated
as
robust
endpoint
approved
for
use
evaluation
drugs
treatment
European
Medicines
Agency.
Although
have
potential
enhance
efficiency
accuracy
trials,
challenges
such
limited
sample
sizes
patient
compliance
persist.
integration
artificial
intelligence
into
data
analysis
progress,
but
further
validation
required
before
strategies
can
be
incorporated
future
trial
methodologies.
Language: Английский
DL-Enhanced GAIT Analysis for Rehabilitation: A Comprehensive Survey
O. Pushpalatha,
No information about this author
R. Premkumar
No information about this author
International Journal of Electrical and Electronics Engineering,
Journal Year:
2024,
Volume and Issue:
11(11), P. 203 - 221
Published: Nov. 30, 2024
Integrating
DL
techniques
has
revolutionized
gait
analysis,
enhancing
the
accuracy
and
efficiency
of
detecting
characterizing
abnormalities.
This
paper
surveys
recent
studies
employing
Deep
Learning
algorithms
(DL),
such
as
Convolutional
Neural
Networks
(CNNs)
Recurrent
(RNNs),
to
analyze
patterns
from
diverse
data
sources
with
wearable
sensors,
video
footage,
motion
capture
systems.
The
advantages
in
handling
complex,
high-dimensional
its
potential
uncover
subtle
indicative
disease
or
recovery
status
are
discussed.
Furthermore,
clinical
applications
DL-based
emphasizing
role
personalized
rehabilitation
programs
real-time
monitoring,
explored.
also
addresses
challenges
implementing
settings,
need
for
large,
annotated
datasets,
computational
resources,
interdisciplinary
collaboration.
In
conclusion,
this
survey
highlights
transformative
methods
analysis
fracture
Parkinson's
patients.
By
providing
a
detailed
overview
current
research
identifying
key
trends
challenges,
work
seems
inform
inspire
further
advancements
field,
ultimately
outcomes
quality
life
affected
individuals.
Language: Английский
Automated Detection of Gait Events and Travel Distance Using Waist-worn Accelerometers Across a Typical Range of Walking and Running Speeds
Albara Ah Ramli,
No information about this author
Xin Liu,
No information about this author
K Berndt
No information about this author
et al.
arXiv (Cornell University),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Jan. 1, 2023
Estimation
of
temporospatial
clinical
features
gait
(CFs),
such
as
step
count
and
length,
duration,
frequency,
speed,
distance
traveled,
is
an
important
component
community-based
mobility
evaluation
using
wearable
accelerometers.
However,
accurate
unsupervised
computerized
measurement
CFs
individuals
with
Duchenne
muscular
dystrophy
(DMD)
who
have
progressive
loss
ambulatory
difficult
due
to
differences
in
patterns
magnitudes
acceleration
across
their
range
attainable
velocities.
This
paper
proposes
a
novel
calibration
method.
It
aims
detect
steps,
estimate
stride
lengths,
determine
travel
distance.
The
approach
involves
combination
observation,
machine-learning-based
detection,
regression-based
length
prediction.
method
demonstrates
high
accuracy
children
DMD
typically
developing
controls
(TDs)
regardless
the
participant's
level
ability.
Fifteen
fifteen
TDs
underwent
supervised
testing
speeds
10
m
or
25
run/walk
(10
MRW,
MRW),
100
(100
6-min
walk
(6
MWT),
free-walk
(FW)
evaluations
while
wearing
mobile-phone-based
accelerometer
at
waist
near
body's
center
mass.
Following
by
trained
evaluator,
were
extracted
from
data
multi-step
process
results
compared
ground-truth
observation
data.
Model
predictions
vs.
observed
values
for
counts,
showed
strong
correlation.
Our
study
findings
indicate
that
single
waist-worn
calibrated
individual's
characteristics
our
methods
accurately
measures
estimates
distances
common
both
TD
peers.
Language: Английский