‘Trying to stay afloat’: Education professionals' perspectives on the impact of the COVID‐19 pandemic on children with special educational needs and disabilities
Journal of Research in Special Educational Needs,
Journal Year:
2024,
Volume and Issue:
24(3), P. 492 - 504
Published: Jan. 30, 2024
Abstract
This
study
aimed
to
investigate
the
experiences
of
education
professionals
in
their
efforts
provide
and
support
children
with
special
educational
needs
disabilities
(SEND)
amid
COVID‐19
pandemic,
gain
insights
into
perceived
repercussions
pandemic‐related
restrictions
on
development
overall
wellbeing
these
children.
Mixed‐methods
surveys
(
N
=
100)
semi‐structured
qualitative
interviews
6)
were
utilised.
Data
analysed
using
descriptive
statistics
thematic
analysis.
Findings
indicate
substantial
challenges
faced
by
delivering
appropriate
effective
well‐being
SEND
during
periods
school
‘closures’,
resulting
hindered
academic
progression
adverse
impacts
SEND,
families
themselves.
It
is
vital
that
strategies
training
are
implemented,
addition
further
research
establish
what
would
be
most
beneficial
for
all
teachers,
particularly
those
supporting
SEND.
Language: Английский
Lessons From the COVID-19 Unplanned Transition to Online Learning at Home for Students With Disability: Socialisation, Technology, Education and Future Research Opportunities
Current Developmental Disorders Reports,
Journal Year:
2024,
Volume and Issue:
11(1), P. 52 - 61
Published: Feb. 1, 2024
Abstract
Purpose
of
Review
Periods
transition
for
children
and
adolescents
with
disability
are
complex
but
usually
anticipated.
The
COVID-19
pandemic
resulted
in
an
unexpected
to
online
learning
at
home
students.
This
review
examines
the
literature
on
students
disabilities
K–12
education
during
identifies
challenges
perceived
benefits
that
emerged
these
inform
future
planned
or
unplanned
transitions
learning.
Recent
Findings
Thirty-one
articles
met
inclusion
criteria.
Overall,
generated
significant
social
technical
disability—ranging
from
inadequate
socialisation
engagement
issues
technological
barriers.
There
were
also
notable
benefits.
For
some
students,
this
included
fewer
pressures,
improvements
mental
health
development
personal
skills
such
as
resilience.
Parent
caregiver
participation
tasks
was
crucial,
often
leading
deeper
insights
into
preferences
needs
ability
tailor
customise
activities.
a
need
inclusive
research
methods
actively
involve
their
experiences.
Furthermore,
predominant
focus
boys
lack
representation
specific
types
support
suggest
larger
studies
should
strive
more
diverse
representative
sample
disability.
Summary
Challenges
reveal
much
about
disruptive
impact
exacted
school-aged
families.
Greater
attention
increasing
access
technologies
required
is
needed.
findings
can
be
applied
adaptation
existing,
implementation
new
modalities,
accommodations
promote
education.
Future
explore
approach
identify
longer-term
impacts
cohorts
ways
schools
plan
effective
event
other
disaster
requiring
school
closures.
Language: Английский
Parent carer and disabled young people’s perspectives on the impacts of changes to service provision for children and young people in England during the COVID-19 pandemic: a qualitative study
BMJ Open,
Journal Year:
2024,
Volume and Issue:
14(11), P. e085144 - e085144
Published: Nov. 1, 2024
Objectives
In
England,
the
delivery
of
health,
education
and
social
care
services
changed
substantially
during
COVID-19.
Some
closed,
some
had
reduced
capacity
there
was
a
shift
to
use
telehealth.
This
study
aimed
understand
how
families
children
young
people
with
neurodisability
experienced
these
service
changes,
what
did
or
not
work
well
for
them
impact
changes
on
them.
Design
Qualitative
parent
carers
(aged
0–19
years)
accessing
children’s
education-based
COVID-19
pandemic.
Setting
Participants
were
recruited
from
five
local
authority
areas
in
England
interviewed
via
telephone
and/or
video
call.
48
(45
mothers,
three
fathers)
nine
8–16
years).
Across
55
(43
males,
12
females),
ranging
3
19
years.
Children
range
diagnoses,
including
autism,
attention
deficit
hyperactivity
disorder,
cerebral
palsy,
genetic
conditions
epilepsy.
Nine
years;
eight
one
female)
interviewed;
two
individually,
focus
group
four
their
carer.
Results
Four
themes
identified:
(1)
communication
(2)
access
pandemic,
(3)
impacts
(4)
learning
future
emergencies
resetting
services.
Communication
reported
as
poor
confusing.
Access
pandemic
varied.
Medical
continued
least
disruption;
therapeutic,
severely
disrupted.
Service
detrimental
coping
high
levels
medical
physical
behavioural
support.
Young
negative
change
physical,
mental
health.
Conclusions
Services
require
person-led,
family
centred
approach
strong
multidisciplinary
team
working.
Findings
indicated
need
improved
within
between
services,
people.
Planning
needs
factor
specific
health
maintain
particular,
those
accessed
through
schools.
Language: Английский
Parent perceptions of social well‐being in children with special educational needs during COVID‐19: A mixed‐methods analysis
Laila Osman,
No information about this author
Jessica Whitley
No information about this author
Child Care Health and Development,
Journal Year:
2024,
Volume and Issue:
50(3)
Published: April 10, 2024
Abstract
Background
Children's
educational
experiences
worldwide
have
been
significantly
impacted
as
a
result
of
global
school
closures
during
the
COVID‐19
pandemic
Spring
2020.
A
growing
number
studies
aim
to
analyse
impacts
these
changes
on
social
well‐being,
with
limited
placing
an
emphasis
students
special
needs
(SENs).
This
article
focusses
parent
perspectives
regarding
well‐being
in
Canadian
children
SEN.
Methods
study
uses
mixed‐methods
approach,
drawing
from
both
qualitative
and
quantitative
survey
data
Spring/Summer
Participants
(
n
=
263)
were
eligible
for
participation
if
they
parent/guardian
child
or
adolescent
We
first
conducted
descriptive
analysis
key
variables,
namely,
grade
level
child,
internet
device
availability,
presence
other
school‐aged
home
(single
vs.
multiple
children).
Next,
we
explored
relationship
between
using
bivariate
correlation.
Finally,
open‐ended
responses
analysed
inductive
approach
thematic
analysis.
Results
The
majority
parents
expressed
concern
their
child's
2020
closures,
increased
concerns
younger
children.
According
parents,
experienced
communication
barriers
peer
interaction
many
emotional
difficulties
result.
Technology
was
described
critical
some
maintaining
connections.
Parents
raised
about
impact
broader
skill
development,
short
long
term.
small
participants
noted
feelings
relief
reduced
anxiety
among
Conclusions
Findings
highlight
views
negative
role
in‐person
schooling
plays
supporting
relationships
Language: Английский
Impact of COVID‐19 lockdown in England on challenging behaviour and adaptive skills for children in a special school: A longitudinal study
British Educational Research Journal,
Journal Year:
2024,
Volume and Issue:
50(4), P. 1765 - 1783
Published: March 4, 2024
Abstract
Longitudinal
research
is
crucial
to
fully
assess
the
putative
impact
of
COVID‐19
pandemic
on
children
with
an
intellectual
disability
in
special
school
settings—ideally
drawing
data
pre‐pandemic
be
able
evaluate
later
impact.
Data
challenging
behaviour
and
adaptive
skills
were
collected
annually
for
348
students
one
across
four
time
points
point
post‐pandemic.
analysed
using
multilevel
models
repeated
observations
over
five
points.
There
was
a
decrease
aggressive
destructive
behaviours
at
post‐pandemic
point,
after
accounting
other
important
covariates.
no
evidence
change
stereotyped
or
self‐injurious
behaviours.
Other
longitudinal
methods
rare,
but
current
findings
are
consistent
previous
reporting
young
people,
particularly
from
parent
reports.
Future
considerations
schools
include
adopting
appropriate
strategies
support
learners
reintegrate
back
into
education.
Further
needed
look
longer‐term
disability.
Language: Английский
Accumulating harm and waiting for crisis: Parents perspectives of accessing Child and Adolescent Mental Health Services for their autistic child experiencing mental health difficulties
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 13, 2024
Background
Autistic
children
and
young
people
are
at
increased
risk
of
mental
health
difficulties,
but
often
face
barriers
when
seeking
help
from
Child
Adolescent
Mental
Health
Services
(CAMHS).
There
is
limited
literature
exploring
the
accessibility
CAMHS
for
autistic
people,
particularly
parents
perspectives.
The
present
study
aimed
to
1)
explore
experiences
parents/carers
their
childs
2)
gain
perceptions
support
child
understand
what
could
be
improved.
Methods
A
mixed-methods
survey
design
was
used
learn
parents/carers.
300
took
part
across
UK
between
June
October
2023.
Quantitative
data
were
analysed
using
descriptive
statistics,
qualitative
content
analysis.
Results
Findings
demonstrated
ongoing
struggles
that
faced
professional
child.
Many
not
referred
or
rejected
without
an
assessment,
due
issues
relating
diagnostic
overshadowing,
a
high
threshold
lack
knowledge
about
autism
care
pathways.
Those
who
reported
reasonable
adjustments
offers
ineffective
inappropriate
therapies,
leaving
unable
engage,
thus
benefiting.
Ultimately,
felt
difficulties
either
did
improve
declined
point
crisis.
However,
there
recognition
some
professionals
kind
compassionate,
provided
validation
needed.
Conclusions
need
more
neuro-inclusive
personalised
approach
in
CAMHS,
themselves,
offered,
therapies
provided.
Further
research,
funding,
training
urgently
needed
ensure
accessible,
timely,
effective
CYP.
Language: Английский
Navigating healthcare during a pandemic: what parents of CHD children want healthcare professionals to know
Cardiology in the Young,
Journal Year:
2024,
Volume and Issue:
35(2), P. 246 - 252
Published: Nov. 21, 2024
The
COVID
pandemic
has
had
deleterious
effects
on
the
mental
health
of
global
population.
Parents
children
with
CHD
were
particularly
vulnerable
to
negative
outcomes
such
as
depression,
anxiety,
and
perceived
stress.
A
better
understanding
parent
experiences,
needs,
concerns
while
navigating
healthcare
system
during
a
is
needed.
Online
survey
responses
from
71
parents
young
representing
families
across
United
States
America
Canada
analysed.
Qualitative
data
collected
one
year
into
pandemic.
Thematic
analysis
was
used
examine
open-ended
question
"What
would
you
like
professionals
(doctors,
nurses)
know
about
your
experience
being
child
COVID-19
pandemic?."
Two
major
themes
subthemes
an
umbrella
theme
emerged
parents'
(1)
Pandemic
Parenting:
Emotional
Toll
Hospital
Visitation
Restrictions,
Dealing
Social
Distancing,
Feeling
Isolated,
Decision
Making
in
Uncertainty,
Playing
it
Safe
versus
Returning
Normal
(2)
Unmet
Expectations
Care:
Needing
Information,
Wanting
Empathy,
Requesting
Respect,
Questioning
Care
Quality,
of:
Our
Lives
Turned
Upside
Down.
describe
impact
healthcare-related
challenges
These
findings
may
offer
insight
how
can
support
care
burden
future
pandemics.
Language: Английский