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44 Cards in this Set

  • Front
  • Back

Intellectual Disability

Originates before age 18


Two standard Deviations below the norm


1-3% of population


More frequently in males

Subcategories of Intellectual Disabilities

1. Mild Intellectual Disability (IQ 50/55-55/70)




2. Moderate (Down Syndrome: IQ 40/45)




3. Severe (IQ 25/40)




4. Profound (IQ below 20/25)

5 Dimensions Associated with Recent Categorizations of Level of Intellectual Disability

1. Intellectual Ability




2. Adaptive Behavior




3. Participation, interactions, and social roles




4. Mental and physical health




5. Context

Causation and Risk Factors

Prenatal (before birth) - Biomedical, Social (poverty, violence, prenatal care), Behavioral (drugs, smoking), Educational




Perinatal (during birth) - Premature birth, lack of birth care, abandonment, etc.




Postnatal (after birth) - TBI, seizure disorder, social deprivation, abuse, etc.

Down Syndrome

Most common genetic cause of ID


Not inherited / Extra 21st chromosome


Loss of hearing / Great Vocab


Communication delay (modalities: sign language/AC system)


Pragmatics are strength (may interrupt)


Reading - strength; Writing - difficult

Fragile X

Mutation of X chromosome


Males are more severely affected


Long face/ears


Severe ID


Increased seizures / Anxiety / ADHD


Receptive language less impaired


Minimally verbal / strong receptive vocab


Difficulties with voice quality


Word finding problems


Pragmatic Difficulties


INTERVENTION: pragmatics, some AAC

William Syndrome
Heart disease, failure to thrive, hearing loss, ID, speech and language delay, anxiety.

Delayed verbal skills / articulation is good


"Overly Friendly"


Pragmatic Difficulties


Language is equivalent to mental age

Angelman Syndrome

Two types - Deletion positive and non-deletion

Hyperactivity, sleep disorders, happiness


Seizures, gait difficulties, issues with vision


Limited Expressive Language - Advanced comprehension skills


Communication: nonverbal skills vary


Intervention: Increase comm. through AAC gestures and voice output devices

Rett Syndrome
Associated with females

Typical until about 12-18 months


4 Stages: onset, rapid destruction, plateau, late motor deterioration stage


Loss use of hands, apraxia, seizures, ID, autistic-like traits


AAC options can include eye gaze and partner assisted scanning

Prader-Willi

Obesity, short stature, intellectual delays


Learning difficulties are present - even when there is typical intelligence


Low-tone may result from Failure to Thrive


Receptive and Expressive Language delays may be associated with intellectual disabilities


Speech Delays may be associated with Hypotonia

Criterion-Referenced Assessment


(why preferred over norm-referenced assessment?)

Spontaneous language sample
Classroom-based assessment,


Interview individual's family, caregiver, and teachers.


Evaluation of AAC devices for some individuals


Evaluation of reading and writing




Limitations of Norm-Referenced:


Not included in normative sample


Lack of Pragmatic Assessments

Functional Assessment

Gather info about behavior to identify purpose




Gain attention


Obtain a desired item


Avoid/Escape


Sensory Stimulus

Functional Communication Training

Behavioral Intervention used to replace problem behaviors with socially acceptable options




Providing opportunities to practice replacement behavior

AAC (Augmentative and Alternative Communication)

Assessment: AAC modes (books, sign language, communication device






Intervention: Modeling, communication opportunities, meaningful communication

Characteristic Deficits of ASD

Communication and Social


Behavioral


Motor/Perceptual


Learning Differences

Communication and Social Differences (ASD)

Difficulties with joint-attention


Less positive emotional affect


Less gestures


Expressive language may include echolalia


Difficulty with peer relationships

Behavioral Differences (ASD)

Hypersensitive (tries to escape too much input)




Hyposensitive (don't notice input; smells, sounds)




Narrow and rigid interests

Motor and Perceptual Differences (ASD)

Delayed motor development




Walking on toes

Learning Differences (ASD)

Memory for symbolic info impaired




Task that require rote memory (visual info) may be intact




Difficulties with empathy (theory of mind)

ASD and Co-occurring Conditions

1 of 68 children in the US have ASD




More males than females (4:1)




Co-occurring conditions:


intellectual disability, seizure disorders

Possible Causes of ASD

Genetic Investigations




Environmental Factors

Assessment and Intervention

Developmental Issues:


Sensorimotor Skills


Joint Visual Attention






Family Involvement



Assessment and Progress Monitoring

Screening: does child need further testing?




Diagnostic Evaluation: Does child have ASD?


Team Approach


Use of Specific Tests




Communication Assessment




Monitoring: Rating scales may be appropriate monitoring tools

Screening VS Diagnostic Tests

Screening: To detect potential disease




Diagnostic: To establish presence/absence of disease

Communication Assessment

Case history, parent interview, observation of child during play, etc.




Evaluate:


joint attention


Verbal/Nonverbal communications


Receptive / Expressive Language


Later Pragmatics: Conversational skills


Literacy skills

Intervention Challenges

Numerous interventions available




Be aware of diff. approaches and evidence behind each approach

Categorizing Approaches

Traditional Behavioral


Contemporary Behavior


Developmental




Targets/Goals - early comm., later pragmatics, AAC, etc.




Whether program is a comprehensive approach or addresses a single skill

ASD Interventions

Early Communication - Early social interaction




AAC




Later Pragmatics - social cognitive, social stories




Reduction of challenging Behaviors - visual supports, FCT

Discrete Trial Training

Specific technique with Applied Behavioral Analysis




Used to teach receptive identification of objects, pic, and actions and verbal labeling




Often taught in home by parents




20-40 hours a week

SCERTS

Social Communication




Emotional Regulation




Transactional Supports




Based on social interaction and family systems theory

What is AAC

Addresses temporary and permanent impairments in spoken and written language




Multi-modal communication: gestures, speech, facial expressions, writing, devices, etc.




Goal:


Vocab - content/semantics


Combining symbols - syntax/morphology


Help with pragmatics

Individuals with Complex Communication Needs

Down Syndrome


Autism Spectrum Disorders


Cerebral Palsy (before, during, or after birth)


Multiple Disabilities


Dual Sensory Impairment (deaf and blind)

AAC symbols

Unaided: talking, gestures, sign language




Aided: picture board, ipad app, device, etc.

AAC Aids

Communication Boards




Dedicated Devices




Simple Digitized Device




Mobile Technologies

AAC Strategies

Prediction: typing a letter and seeing a list of possible words






Encoding: group of letters (LOL)

Direct Selection




VS




Scanning

Direct Selection: pointing with a finger, mouthstick, light, etc.




Scanning: require less motor control. involves use of light to pass over each choice

Selection Sets

Fixed Displays - symbols that don't change




Dynamic Displays - changes after you click on one image to another set of images (phone)




Visual Scene Display - a picture that represents situation, experience, or place.

AAC Assessment

Team Effort: family, occupational therapist, special ed teacher, psychologist, etc.




Test: literacy, hearing, vision, oral-motor, speech, cognition, and physical skills




Trial use of AAC systems



Participation Model: Determine comm. needs and participation patterns. Participation Barriers.

Symbol Assessment

Select Symbols that meet individual's needs




Aided/Unaided




Match Target Object With:


other objects, pics, line drawings, written words.




Use of symbols within natural interactions

Feature Matching

Looking at each client's skills and abilities and finding the device/system that best matches that individual's needs.

System for Augmenting Language (SAL)

Speech Generating Device (SGD)

Symbols with English printed above


Communication Opportunities


Comm. Partner uses symbols


Core Words: frequently used


Fringe Words: words specific to that person

Visual Scene Displays

Low or High Technology




Realistic nature maximizes meaningfulness and organizes language concepts within categories

Picture Exchange Communication System (PECS)

Used with children who are on the autism spectrum


Goal is to teach functional communication


Based on principles of applied behavior analysis


6 Phases

6 Phases of PECS

1. Teaching the communicative exchange


2. Teaching persistence


3. Discrimination training


4. Teaching 'I want" sentences


5. Teaching a response to "what do you want?"


6. Teaching use of additional sentence starters