BACKGROUND
Exercise
is
crucial
for
individuals
with
paraplegia
to
reduce
the
risk
of
secondary
diseases
and
improve
independence
quality
life.
However,
numerous
barriers
such
as
inadequate
accessibility
restrict
their
participation
in
exercise
programs.
Digital
apps
can
help
overcome
these
barriers.
Personalization
considered
a
feature
mobile
apps,
people
have
individual
requirements
regarding
programs
depending
on
level
impairment.
Despite
increasing
popularity
there
are
none
available
that
target
needs
this
cohort.
The
ParaGym
app
prototype
was
designed
automatically
tailor
sessions
users
paraplegia.
OBJECTIVE
This
study
aims
evaluate
feasibility,
usability,
safety,
preliminary
effectiveness
prototype.
METHODS
pilot
block-randomized
controlled
feasibility
trial
will
include
45
adult
participants
Eligible
be
block
randomized
either
intervention
or
waitlist
control
group.
group
perform
6-week
program
using
app,
comprising
three
35-minute
per
week.
continue
usual
care
receive
access
after
completion.
Participants
record
all
conducted
well
additional
during
period
diaries.
primary
outcomes
safety.
Feasibility
assessed
through
semistructured
interviews,
adherence,
retention
rates.
Usability
measured
System
Scale.
Safety
determined
by
occurrence
adverse
events.
Secondary
effects
peak
capacity
(VO<sub>2</sub>
peak);
handgrip
strength;
independence,
which
Spinal
Cord
Independence
Measure
III
(SCIM
III);
health-related
life,
Short
Form–36
Health
Survey
(SF-36).
RESULTS
Recruitment
commenced
November
2022.
Overall,
12
were
enrolled
at
time
submission.
Data
collection
January
2023,
completion
expected
April
2023.
CONCLUSIONS
To
best
our
knowledge,
first
assess
safety
an
intelligent
Thereafter,
should
adapted
according
findings
trial.
Future
trials
updated
version
aim
larger
sample
size,
longer
duration,
more
diverse
In
long
term,
fully
marketable
implemented.
would
increase
personalized,
independent,
evidence-based
training
cohort
and,
future,
other
who
use
wheelchairs.
CLINICALTRIAL
German
Clinical
Trials
Register
DRKS00030370;
https://drks.de/search/de/trial/DRKS00030370
INTERNATIONAL
REGISTERED
REPORT
DERR1-10.2196/45652
Health data management,
Год журнала:
2024,
Номер
unknown, С. 323 - 336
Опубликована: Янв. 1, 2024
Wearable-Technologien
stellen
kontinuierlich
Gesundheitsdaten
bereit
und
können
Ärzte
bei
Diagnose,
Überwachung
Therapie
unterstützen.
Während
ihre
Praktikabilität
in
den
Bereichen
Fitness
Unterhaltung
bereits
bewiesen
ist,
erfordert
Anwendung
im
Gesundheitswesen
für
Biomarker-Tracking
jedoch
Standardisierung,
Workflow-Kompatibilität
nahtlose
Datenintegration.
Digitale
Gesundheitsanwendungen
(DiGAs)
sind
medizinisch
zertifiziert
nutzenbringend,
erfordern
Interoperabilität,
Sicherheit,
Patientenorientierung
sowie
Zusammenarbeit
mit
elektronischen
Patientenakten
(ePA),
Versicherungsplattformen
Telemedizin.
Die
laufenden
Standardisierungsbemühungen,
insbesondere
Hinblick
auf
HL7
FHIR,
zeigen
vielversprechende
Ansätze
die
Integration
von
Wearables
eHealth.
Definition
geeigneten
Profilen,
strukturierte
Datenkodierung
Entwicklung
der
nötigen
Infrastruktur
Schlüsselfaktoren
eine
gelungene
Umsetzung.
BACKGROUND
Preconception
health
is
essential
for
preventing
premature
birth,
yet
engagement
in
preconception
care
remains
low.
Despite
the
development
of
several
internet-based
interventions
post-COVID-19,
a
thorough
evaluation
their
effectiveness
enhancing
and
births
necessary.
OBJECTIVE
This
systematic
review
aims
to
assess
study
designs
evaluate
birth
among
preconceptional
women
childbearing
age.
METHODS
We
conducted
comprehensive
search
MEDLINE,
Embase,
CINAHL,
Cochrane
Library
databases
identify
randomized
trials
quasi-experimental
studies
on
birth.
The
was
global
included
published
up
December
2023,
without
language
or
geographic
restrictions.
Two
authors
independently
assessed
risk
bias
using
revised
RoB
tool
(RoB
2),
adhering
PRISMA
guidelines.
A
meta-analysis
not
due
heterogeneity
populations,
measurements,
interventions.
RESULTS
Eleven
articles
were
included,
with
varying
approaches.
overall
high
most
studies.
Interventions
improved
knowledge
reproductive
but
had
no
significant
effect
self-efficacy
related
promotion.
While
some
behavioral
changes
reduce
risks
effectively
promoted,
impacts
folic
acid
use,
contraception
initiation,
dual
method
use
inconsistent.
Furthermore,
there
reductions
sexually
transmitted
infections
unplanned
pregnancies.
CONCLUSIONS
Internet-based
showed
mixed
across
different
outcomes,
general
ineffectiveness
improving
status.
results,
derived
from
limited
number
bias,
suggest
need
caution
application.
Future
research,
including
robust
clinical
trials,
vital
develop,
evaluate,
disseminate
effective
safe
care.
CLINICALTRIAL
PROSPERO
CRD42021277024;
https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42021277024
Technologies,
Год журнала:
2023,
Номер
11(3), С. 66 - 66
Опубликована: Май 1, 2023
Mobile
fitness
applications
(apps)
allow
for
time-efficient
opportunities
physical
activity.
Current
research
suggests
that
apps
do
not
accurately
comply
with
the
frequency,
intensity,
time,
and
type
(FITT)
principle.
FITT
is
an
important
principle
in
exercise
prescription
as
it
applies
scientific
evidence
to
improve
quality
of
exercise.
Based
on
app
assessment
using
Fitness
Apps
Scoring
Instrument,
most
adequately
address
their
plans.
In
particular,
adhere
intensity
guidelines.
Many
users
track
heart
rate
a
method
assessing
but
few
use
information
provide
real-time
feedback
workout.
For
users,
awareness
education
standards
should
be
put
forth
coordination
professionals,
rather
than
relying
alone.
BACKGROUND
Most
smokers
are
ambivalent
about
quitting—they
want
to
quit
someday,
but
not
now.
Interventions
needed
that
can
engage
smokers,
build
their
motivation
for
quitting,
and
support
future
attempts.
Mobile
health
(mHealth)
apps
offer
a
cost-effective
platform
such
interventions,
research
is
inform
optimal
design
assess
acceptability,
feasibility,
potential
effectiveness.
OBJECTIVE
This
study
aims
the
impact
of
novel
mHealth
app
who
smoking
someday
quitting
in
near
term.
METHODS
We
enrolled
adults
across
United
States
smoked
more
than
10
cigarettes
day
were
(n=60).
Participants
randomly
assigned
1
2
versions
GEMS
app:
standard
care
(SC)
versus
enhanced
(EC).
Both
had
similar
identical
evidence-based,
best-practice
cessation
advice
resources,
including
ability
earn
free
nicotine
patches.
EC
also
included
series
exercises
called
experiments
designed
help
clarify
goals,
strengthen
motivation,
learn
important
behavioral
skills
changing
behavior
without
making
commitment
quit.
Outcomes
analyzed
using
automated
data
self-reported
surveys
at
3
months
post
enrollment.
RESULTS
installed
(57/60,
95%)
largely
female,
White,
socioeconomically
disadvantaged,
highly
dependent.
As
expected,
key
outcomes
trended
favor
group.
Compared
SC
users,
participants
greater
engagement
(mean
sessions
19.9
vs
7.3
SC).
An
intentional
attempt
was
reported
by
39.3%
(11/28)
users
37.9%
(11/29)
users.
Seven-day
point
prevalence
abstinence
3-month
follow-up
14.7%
(4/28)
6.9%
(2/29)
Among
earned
trial
replacement
therapy
based
on
usage,
36.4%
(8/22)
11.1%
(2/18)
requested
treatment.
A
total
17.9%
(5/28)
3.4%
(1/29)
used
an
in-app
feature
access
tobacco
quitline.
Other
metrics
promising.
completed
average
6.9
(SD
3.1)
out
9
experiments.
Median
helpfulness
ratings
ranged
from
4
5-point
scale.
Finally,
satisfaction
with
both
very
good
4.1
Likert
scale)
95.3%
(41/43)
all
respondents
would
recommend
version
others.
CONCLUSIONS
Ambivalent
receptive
app-based
intervention,
version,
which
combined
self-paced,
experiential
exercises,
associated
use
evidence
change.
Further
development
evaluation
program
warranted.
CLINICALTRIAL
ClinicalTrials.gov
NCT04560868;
https://clinicaltrials.gov/ct2/show/NCT04560868
Nutrients,
Год журнала:
2023,
Номер
15(16), С. 3606 - 3606
Опубликована: Авг. 17, 2023
In
the
last
decade,
we
have
seen
a
substantial
increase
in
development
and
use
of
mobile
technology
to
improve
diet
healthy
eating
behaviors.
To
describe
characteristics
nutrition
apps
before
after
COVID-19
pandemic
available
Brazil.
Nutrition
were
identified
using
official
Apple
Google
stores.
The
search
occurred
January
2020
May
2022
We
extracted
nutritional
content
standard
indicators
(e.g.,
being
developed
or
2020,
number
languages,
target
population,
investment,
prices,
seller,
reviews
downloads,
consumer
rating).
280
launched
411
during
period.
Most
at
least
ten
languages
(96.6%),
with
no
indication
age
(95.6%)
partial
full
cost
(59%).
As
for
contents,
18.9%
addressed
personal
suggestions;
73.4%,
education;
48.8%,
revenues;
35.9%,
physical
activity
guide;
2.3%,
recommendation
out;
23.9%,
grocery
shopping
scan
code;
32.4%,
food
diary;
18.9%,
water
intake;
4.6%,
nutrition/diseases.
data
show
an
evolution
that
may
been
boosted
by
reveals
trend
towards
educational
content.
During
pandemic,
there
was
positive
qualitative
quantitative
movement
e-health
regarding
promotion
education.
BACKGROUND
Exercise
is
crucial
for
individuals
with
paraplegia
to
reduce
the
risk
of
secondary
diseases
and
improve
independence
quality
life.
However,
numerous
barriers
such
as
inadequate
accessibility
restrict
their
participation
in
exercise
programs.
Digital
apps
can
help
overcome
these
barriers.
Personalization
considered
a
feature
mobile
apps,
people
have
individual
requirements
regarding
programs
depending
on
level
impairment.
Despite
increasing
popularity
there
are
none
available
that
target
needs
this
cohort.
The
ParaGym
app
prototype
was
designed
automatically
tailor
sessions
users
paraplegia.
OBJECTIVE
This
study
aims
evaluate
feasibility,
usability,
safety,
preliminary
effectiveness
prototype.
METHODS
pilot
block-randomized
controlled
feasibility
trial
will
include
45
adult
participants
Eligible
be
block
randomized
either
intervention
or
waitlist
control
group.
group
perform
6-week
program
using
app,
comprising
three
35-minute
per
week.
continue
usual
care
receive
access
after
completion.
Participants
record
all
conducted
well
additional
during
period
diaries.
primary
outcomes
safety.
Feasibility
assessed
through
semistructured
interviews,
adherence,
retention
rates.
Usability
measured
System
Scale.
Safety
determined
by
occurrence
adverse
events.
Secondary
effects
peak
capacity
(VO<sub>2</sub>
peak);
handgrip
strength;
independence,
which
Spinal
Cord
Independence
Measure
III
(SCIM
III);
health-related
life,
Short
Form–36
Health
Survey
(SF-36).
RESULTS
Recruitment
commenced
November
2022.
Overall,
12
were
enrolled
at
time
submission.
Data
collection
January
2023,
completion
expected
April
2023.
CONCLUSIONS
To
best
our
knowledge,
first
assess
safety
an
intelligent
Thereafter,
should
adapted
according
findings
trial.
Future
trials
updated
version
aim
larger
sample
size,
longer
duration,
more
diverse
In
long
term,
fully
marketable
implemented.
would
increase
personalized,
independent,
evidence-based
training
cohort
and,
future,
other
who
use
wheelchairs.
CLINICALTRIAL
German
Clinical
Trials
Register
DRKS00030370;
https://drks.de/search/de/trial/DRKS00030370
INTERNATIONAL
REGISTERED
REPORT
DERR1-10.2196/45652