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| Dear Reader,
ACT would like to welcome you to our first
quarterly newsletter! This newsletter is designed
to give you access to important research in the areas of
Autism Spectrum Disorders and highlight and discuss
various behavior management techniques. We hope to
bring useful information to our readers! Please
let us know if you have any topics of interest that you
would like to learn more
about. | |
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Time to Learn
More About Time Outs!
When
used properly, timeouts can be a very effective tool to
keep in you behavior toolbox! Time out is a
form of negative punishment in which a positive
experience or environment is removed with the intent of
decreasing a maladaptive behavior.
As always, before any punishment is
necessary, there are many antecedent strategies (i.e.,
strategies you can employ before the behavior occurs)
that will greatly help decrease an unwanted
behavior.
When devising behavior management plans, it is
very important to make sure that you are using both
antecedent and consequence strategies. A balanced plan
will change behavior most effectively. Using antecedent
strategies will set your child up for success so that
you will not have to rely on consequences as often.
Some very useful antecedent strategies
include priming (e.g., reminding your child of the rules
before starting an activity), teaching functional
communication skills, replacing the unwanted behavior
with an incompatible behavior and anger management
techniques. While
antecedent strategies are useful and necessary,
there will still be times when consequence
strategies will be needed. In this case,
time outs may be very effective.
It is important to use timeouts
only when "time in" is fun. Make sure that
you are removing the child from an activity that he/she
will miss.
For example, if your child is swimming in the
pool (an activity that he considers very enjoyable) and
he hits his sibling, time out from the pool would be a
very appropriate consequence because he will miss being
in the pool.
Essentially you are teaching him that if he
doesn't behave properly in the pool, he can not
have the privilege of swimming in it. Another way to
ensure that time outs are effective is to have a time
out area that is "boring" and relatively free of
stimulation.
Time out should not take place in an area with
toys or fun objects.
Time outs should be avoided in
situations when "time in" will not be missed by the
child. For
example, if you are helping him with homework (an
activity he doesn't find enjoyable) and he engages in an
aggressive behavior, a time out may not be the most
effective consequence. Instead of seeing the time out as
a punishment, he may see it as a break from
homework.
In this case you might have inadvertently
reinforced a behavior you wanted to decrease! In
situations like these you will have to choose a
different consequence technique.
Here are a few more tips for using
timeout effectively: 1) use a calm voice and demeanor
when escorting your child to the time out area, 2) use a
simple phrase, "No hitting. Time out", 3) when time out
is over, do not immediately engage in conversation or
give your child too much attention - this may make the
time out reinforcing and 4) do not "over-use" this
technique - your child may get used to time outs and it
will lose it's power as an effective punisher. If you wish to
discuss the behavior with him you may certainly do so
before the behavior occurs (as another antecedent
strategy) or after the consequence, but not in the
moment.
Remember that time outs are only one of
many effective consequences and that a balanced plan
with both antecedent and consequence strategies will
reduce unwanted behaviors most
effectively.
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PECS Training May Increase the
Production of Spoken Words in Children with
Autism
Deborah Carr and Janet Felce, two
researchers in Wales, United Kingdom, recently published
an article in the Journal of Autism and Developmental
Disorders describing an experiment they conducted. The
experiment investigated the results of PECS training
through Phase III on speech production in children
diagnosed with Autism (Carr & Felce, 2007).
The Picture Exchange Communication System
(PECS; Bondy & Frost, 1994) is an augmentative
communication system designed to increase functional
communication in children. Bondy and Frosty
(1994, p. 3) define the fundamental goal of PECS:
"Children are taught to approach and give a picture of a
desired item to a communicative partner in exchange for
that item.
By doing so, the child initiates a communicative act
for a concrete item
within a social context."
PECS is
taught in six phases. Phase I focuses
on the initial exchange. Phase II teaches the child to
travel to a communicative partner to initiate a request
and Phase III focuses on discrimination between
pictures.
Phase IV teaches using a sentence strip to
communicate. Phase V teaches the child to respond to the
question, "What do you want?", and Phase VI teaches the
child to use pictures to comment both spontaneously and
responsively (Carr & Felce, 2007).
In Carr and Felce's study, children
between the ages of 3 and 7 who were diagnosed with
Autism were divided into two groups. One group, the
experimental group, received 15 hours of PECS training
through Phase III in their school environment. The control
group did not receive any PECS training or any
treatments beyond the interventions they were already
receiving in school. Assessments for
use of language for all children were conducted at three
points: five weeks prior to treatment, one week prior to
treatment and one week after the completion of
treatment.
Treatment lasted approximately 4 to 5 weeks. The
observations of the experimental group and control group
were compared.
Results indicated that overall the
children who received the PECS training acquired more
spoken words during the treatment phase than those who
didn't receive the training. Specifically,
three children who already used some spoken words during
the first two observations increased their total words
produced at the post-treatment observation. Two children in
the PECS group, who did not speak words at the first two
observations, used spoken words at the post-treatment
observations.
In the control (non PECS) group, one child
demonstrated a small increase (two words) in total words
at the post-treatment observation. The four other
children in the control group demonstrated decreases in
total words spoken at the final observation. The number of
participants was too small to conduct statistical
analyses of the data; however, the results reinforce the
current view that teaching the use of picture exchange
could promote speech in some children.
It is worth noting that the teaching
protocols were applied according to the PECS program
which precludes the purposeful teaching of speech. Yet, despite the
fact that there was no deliberate attempt to teach
spoken language, the children who received PECS training
demonstrated increases in spoken words. The authors
speculate that the reason this increase in spoken
language is observed is because, in PECS training, the
person who is receiving the picture from the child
repeats the item clearly to the child during the
exchange.
Therefore, the combination of the spoken word,
physical item and picture of the item all at once may
clarify the meaning of the word for the child. This
might facilitate the eventual use of the spoken word
without the
picture. |
Ryan's Story
ACT
would like to introduce our readers to Ryan and his
family: his mother LeeAndra, his father Dan and his
sister Jenna! Ryan is a bright, motivated, charismatic
and loving five year old boy. He has also been
diagnosed with Autism. Ryan came to ACT when he was just
two years old and, at the time, he did not use spoken
language.
His mother LeeAndra recalls that he would scream
or tantrum to express emotions and needs. Ryan would pull
people in the direction of desired objects, but he never
uttered words. ACT's therapists and Ryan's family began
using the Picture Exchange Communication System (PECS)
to help him functionally request items. They began to
teach food items, since that is what Ryan was most
motivated for.
LeeAndra recalls that he quickly learned how to
request milk and other foods and drinks.
Once he began using PECS well, Ryan's
therapists and family introduced sign language by
pairing signs with the pictures he used for PECS. Ryan took to
this very quickly and was soon using sign language and
PECS equally well.
Approximately one year ago, Ryan's therapists and
family decided to use sign language as Ryan's primary
form of communication. Words that were signed by either
Ryan or another person were spoken aloud as the sign was
being used. Six months later, to everyone's delight,
Ryan began making vocal approximations of the words he
was signing. As time went on, Ryan's vocalizations
improved and he decreased his use of sign language.
Now, Ryan uses very few signs and
utilizes spoken words as his primary form of
communication.
With prompting he uses three to five word
sentences to request items (e.g., "I want milk please
mommy") and comment on what he sees and feels. LeeAndra says
that he teases his older sister, Jenna, by standing
close to her and repeating everything she says. He
sings his favorite songs loudly in the living
room. Ryan is learning new words
steadily.
The fact that Ryan now uses spoken
language to communicate has changed his family's
life.
LeeAndra comments that she now knows that he can
understand what she says to him, which is a great
relief. Much of the time, instead of screaming or
tantrumming, he expresses his feelings
appropriately.
His use of language has opened the door for many
new learning opportunities.
Ryan's mother credits Ryan for his
accomplishments.
She says he is motivated to learn and that he has
done a lot of hard work. LeeAndra
specifically requested that thanks be given to the ACT
therapists Richelle, Aimee, and Doug who have had, and
will continue to have, an active role in Ryan's
learning.
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We hope that you've enjoyed the first issue of
ACT's Newsletter and have found it useful. Pease
contact us if there are topics you would like to
see addressed in the newsletter. You may
suggest topics by sending an email to Sarah.Pashalides@AutismCenterforTreatment.com.
Look for our next issue in July, 2008!
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