Journal of Alzheimer s Disease,
Journal Year:
2024,
Volume and Issue:
100(2), P. 469 - 473
Published: June 11, 2024
Caregiving
for
a
person
with
dementia
is
considered
situation
of
chronic
stress,
consequences
on
caregivers'
physical
and
psychological
health.
The
usual
challenges
care
were
intensified
during
the
pandemic
due
to
risk
contagion,
social
isolation
measures,
decrease
in
healthcare
resources.
COVID-19
increased
stress
both
persons
their
caregivers.
This
commentary
reflects
long-term
effects
mental
health,
focusing
study
by
Olavarría
colleagues
drawing
future
research
lines
culturally
diverse
family
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(5), P. e27351 - e27351
Published: Feb. 29, 2024
Older
adults
with
chronic
illness,
as
well
their
primary
caregivers
in
multigenerational
families,
may
experience
a
complex
interplay
of
factors
that
affect
quality
life
(QOL).
However,
this
is
not
yet
well-characterized
for
Chinese
families
particular.
In
study,
we
analyzed
how
family
resilience
and
social
support
the
QOL
both
older
specifically.
We
enrolled
258
pairs
illness
multicenter
cross-sectional
study
conducted
southern
China
December
2021.
Using
Actor-Partner
Interdependence
Model
(APIM),
then
examined
correlation
between
resilience,
support,
dyadic
analysis
found
QOL,
were
better
than
those
(
Palliative & Supportive Care,
Journal Year:
2025,
Volume and Issue:
23
Published: Jan. 1, 2025
Recent
studies
have
challenged
the
assumption
that
families
are
invariable
sources
of
support
for
cancer
caregivers,
noting
relationships
with
family
members
can
both
positive
and
negative
effects
on
caregiver
well-being.
This
study
expands
upon
prior
literature
to
examine
relationship
between
caregivers'
perceptions
quality
their
interactions
symptoms
anxiety.
We
employed
secondary
analysis
baseline
data
from
a
multisite
randomized
clinical
trial
an
intervention
caregivers
conducted
at
3
large
academic
palliative
care
clinics.
performed
linear
regression
analyses
analyze
anxiety;
additional
models
were
estimated
further
characterize
this
addition
relevant
covariates:
race,
ethnicity,
sex,
marital/relationship
status,
patient,
employment
household
income,
perceived
social
received
friends
significant
others.
also
sub-analysis
provided
by
who
married
or
partnered
anxiety
satisfaction
as
covariate.
Among
our
analytic
sample
(n
=
244),
we
identified
remained
statistically
covariates.
Relationship
was
not
found
be
covariate
in
caregivers.
Study
results
provide
strong
development,
testing,
implementation
interventions
improve
strategy
reduce
Innovation in Aging,
Journal Year:
2025,
Volume and Issue:
9(4)
Published: Jan. 1, 2025
Informal
caregiving
for
older
adults
can
be
both
burdensome
and
beneficial.
Given
that
the
informal
situation
may
evolve
over
time,
care
needs
of
result
from
diverse
health
conditions,
it
is
valuable
to
understand
trajectories
burden
or
benefits
how
these
vary
across
conditions
common
among
care-recipients.
This
review
first
summarize
literature
on
caregiving,
including
caregiver
care-recipient
characteristics
associated
with
trajectories.
We
reviewed
longitudinal
observational
quantitative
studies,
5
bibliographic
databases,
assessed
at
3
more
time
points
caregivers
(60
years
above).
The
narrative
synthesis
included
41
only
7
(17%)
considering
benefits.
A
stable
average
trajectory
was
most
pattern
various
conditions.
However,
an
increasing
primarily
observed
persons
dementia,
while
a
decreasing
noted
discharged
hospital
after
acute
event.
Only
6
(10%)
which
reported
heterogeneity
in
progression
separately
jointly,
identified
distinctive
within
same
set
caregivers.
Risk
factors
consistently
indicating
persistently
higher
lower
functional
limitations
behavioral
problems,
being
non-spousal
caregiver,
solo
perceiving
less
self-efficacy
competence.
Future
studies
should
focus
untangle
consider
concurrently
identify
enhance
alleviate
time.
BACKGROUND
The
global
rise
in
ageing
populations
is
expected
to
significantly
increase
the
demand
for
informal
care.
Informal
carers
are
crucial
healthcare
systems
but
often
face
physical,
mental,
and
emotional
challenges
due
demands
of
caregiving.
Open
online
courses
have
emerged
as
potential
tools
support
by
providing
accessible,
flexible
learning
opportunities.
However,
landscape
these
remains
underexplored,
particularly
concerning
their
design,
outcomes,
barriers
enablers
participation.
OBJECTIVE
This
systematic
review
aimed
map
characteristics
open
carers,
explore
learner
experiences,
identify
participation
inform
design
future
courses.
METHODS
We
systematically
searched
four
electronic
databases
studies
published
from
inception
30
January
2025:
(1)
APA
PsycINFO,
(2)
CINAHL,
(3)
EMBASE,
(4)
MEDLINE.
Two
reviewers
independently
screened
titles
abstracts
eligibility.
Included
reported
on
development,
delivery,
or
outcomes
using
quantitative,
qualitative,
mixed
methods
designs.
Backward
forward
citation
was
conducted
reference
lists
included
studies.
Data
study
methodology,
course
characteristics,
evaluations
were
extracted
synthesised
narratively.
quality
quantitative
assessed
Effective
Public
Health
Practice
Project
(EPHPP)
Quality
Assessment
Tool,
qualitative
Critical
Appraisal
Skills
Program
(CASP)
toolkit.
Mixed
appraised
both
tools.
RESULTS
database
search
identified
200
studies,
with
an
additional
through
backward
citation.
Following
screening,
10
(6
4
methods)
met
eligibility
criteria
inclusion.
All
examined
massive
(MOOCs)
varied
length
content.
primarily
targeted
older
individuals
dementia
chronic
conditions
such
multiple
sclerosis.
Learner
benefits
improvements
knowledge,
caregiving
skills,
application
gains
into
everyday
scenarios.
Learners
accessibility
approaches
key
benefits.
related
interactivity,
peer
engagement,
learners
varying
levels
digital
literacy
internet
access
emphasised.
Nine
ten
papers
demonstrated
moderate
weak
methodological
EPHPP
tool,
three
CASP
toolkit,
limitations
participant
selection,
blinding,
presentation
data.
CONCLUSIONS
can
provide
accessible
education
that
improves
knowledge
skills
learners.
poor
limited
opportunities
interaction
will
be
helpful
areas
address
incorporation
synchronous
elements
including
live
moderated
discussions,
along
more
technical
options,
could
enhance
experience.
Further
high-quality
research
essential
extend
strengthen
evidence
base
guide
development
effective
educational
resources
carers.
CLINICALTRIAL
PROSPERO
CRD42024532766;
https://www.crd.york.ac.uk/PROSPERO/display_record.php?
RecordID=532766
International Psychogeriatrics,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100052 - 100052
Published: Feb. 1, 2025
This
study
aims
to
analyze
the
association
between
care-specific
psychosocial
factors
in
terms
of
familism,
care
stigma,
caregiver
burden,
and
gains
with
suicidal
ideation
informal
caregivers
older
adults
Germany.
Data
from
Attitudes
Towards
Informal
Caregivers
Project
(ATTIC)
433
aged
≥
60
years
was
used
research
question.
The
Internalized
Caregiver
Stigma
Scale
measure
internalized
attitudes
behavior
regarding
provision
for
adults,
measuring
passive
suicide
thoughts,
were
measured
positive
aspects
scale
familism
short
attitudinal
scale.
Linear
regression
analysis
robust
standard
errors
calculated
adjusted
contextual
personal
(e.g.,
co-residence,
personality,
social
support).
Stronger
beliefs
negative
stigma
associated
higher
frequency
while
stronger
not
significantly
ideation.
associations
also
found
additional
a
log-transformed
outcome
analyses
excluding
mental
health
as
covariate
(except
which
ideation).
Care-specific
are
important
risk
Thus,
changing
evaluations
expectations
about
its
performance
could
be
helpful
prevent
experiencing
(high
levels
of)
Journal of Aging and Health,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 10, 2025
Objective
We
compared
pain
prevalence
and
intensity
between
caregivers
non-caregivers,
as
well
different
types
of
caregivers.
Method
Using
two
rounds
data
from
the
National
Social
Life,
Health,
Aging
Project,
we
used
regression
models
to
analyze
differences
in
non-caregivers
at
baseline
(2010–2011)
follow-up
(2015–2016).
The
sample
consisted
2332
participants
aged
62
older
(352
1980
non-caregivers).
Results
Cross-sectionally,
were
more
likely
than
report
pain.
Longitudinally,
with
presence
greater
five
years
later
who
also
reported
baseline.
More
hours
care
per
week
was
associated
among
Discussion
Caregivers’
is
a
public
health
concern,
efforts
mitigate
effects
caregiving
on
needed.
Epidemiology,
Journal Year:
2025,
Volume and Issue:
36(3), P. 297 - 305
Published: April 1, 2025
Background:
Previous
evidence
shows
that
religious
service
attendance
is
associated
with
lower
mortality
among
women
and
fewer
hospitalizations
men.
However,
it
unclear
if
similar
associations
exist
for
other
activities.
Methods:
This
cohort
study
examines
the
between
various
activities
their
engagement
levels
on
2987
Danes
aged
40+
years,
interviewed
in
SHARE
from
2004
to
2007.
The
followed
individuals
Danish
registers
until
2018.
We
estimated
relative
absolute
risks
of
at
age
90
used
negative
binomial
regressions
hospitalizations,
including
adjustment
several
potential
confounders.
Results:
Overall,
activity
participation
was
mortality.
Specifically,
participating
voluntary
or
charity
work
(relative
[RR]
=
0.85;
95%
CI
0.76,
0.95;
risk
differences
[RD]
−0.11;
−0.18,
−0.04),
helping
others
(RR
0.88;
0.82,
RD
−0.09;
−0.14,
sports
social
clubs
0.89;
0.81,
0.98;
−0.15,
−0.03)
exhibited
found
who
took
part
a
organization.
Our
results
showed
men
engaged
3+
activities,
For
some
strength
varied
frequency;
example,
caring
sick
but
only
when
done
less
than
once
week.
Conclusions:
Several
were
mortality,
particularly
women.
reduced
observed
attending
services
did
not
extend
BMC Psychiatry,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: April 18, 2025
Iran's
demographic
trends
indicate
significant
aging,
with
intensive
caregiving
linked
to
mental
health
issues
among
caregivers,
especially
during
the
Covid-19
pandemic.
This
study
aimed
evaluate
impact
of
Mehrpishegan's
web-based
intervention
on
depression,
anxiety,
and
stress
levels
informal
primary
caregivers
older
adults
in
Iran.
was
a
parallel-group,
superiority,
single-blinded
randomized
controlled
trial
conducted
Tehran.
Eligible
participants
were
responsibility,
access
internet
smart
device,
at
least
one
month
experience,
ability
use
intervention.
The
outcomes
measured
baseline,
3
months,
6
months
using
DASS-21.
Participants
mild
moderate
baseline
into
(n
=
83)
control
80)
groups.
group
accessed
website,
which
provided
structured
educational
content
chatrooms(psychologist-led
for
three
then
peer-led).
Engagement
via
session
attendance,
forum
participation,
material
usage.
Data
analyzed
repeated
measures
ANOVA
based
intention-to-treat
(ITT)
per-protocol
approaches.
Of
participants,
128
completed
final
assessment
six
resulting
an
attrition
rate
20%.
showed
small
decrease
depression
(10.23
±
0.80
vs.
10.48
0.75,
diff
0.253;
95%
CI
-0.24,
1.94),
anxiety
(6.70
0.64
7.86
0.60,
1.17;
-2.93,
0.59),
(13.94
0.78
15.16
0.74,
1.22;
-3.37,
0.92),
but
none
these
differences
statistically
(p
>
0.05).
Effect
size
calculations
indicated
reductions
(d
-0.30)
-0.28)
though
remained
below
threshold
clinical
significance
(|d|
<
0.5).
Although
some
improvements
caregivers'
outcomes,
changes
not
significantly
different
from
those
group.
Several
challenges,
including
disruptions,
voluntary
COVID-19
pandemic,
may
have
influenced
outcomes.
To
enhance
effectiveness
support
programs,
future
interventions
must
overcome
technological
barriers,
strengthen
digital
competencies,
tailor
individual
needs,
address
key
risk
factors.
A
more
personalized
accessible
approach
could
improve
engagement
long-term
benefits
caregivers.
protocol
this
research
registered
Iran
Randomized
Clinical
Trial
Center
registration
number
IRCT2
02010
12,048
999N1
25
December
2020.
Frontiers in Psychiatry,
Journal Year:
2025,
Volume and Issue:
16
Published: April 29, 2025
Introduction
Although
informal
caregivers
are
the
primary
providers
of
long-term
care
for
elderly
globally,
research
on
impact
caregiving
experiences
well-being
is
relatively
limited.
Methods
This
study
conducted
interviews
with
297
family
in
Shanghai,
measured
their
subjective
burdens,
and
applied
valuation
method
to
calculate
monetary
value
welfare
changes
resulting
from
burdens.
Results
According
findings,
sub-dimensions
Chinese
version
Caregiver
Reaction
Assessment
(CRA)
disrupted
schedule,
lack
support,
self-esteem
were
significantly
related
caregivers’
well-being.
For
average
income
CRA
scores,
level
was
equivalent
a
monthly
reduction
226.69
RMB
(4.7%
income).
Discussion
paper
provides
new
useful
perspective
evaluation
policies,
suggests
prioritizing
alleviation
schedule
social
relationship
understanding
‘intrinsic
coping
mechanisms’
responses
an
economic
perspective.