Assessment of Stuttering Flashcards

1
Q

Why do we assess?

A

Get useful info
Understand the history and development of their disorder
To get a starting point
Set goals

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2
Q

What are the Principles of Assessment?

A
  • Explore the impact that stuttering has had
  • Explore the impact of previous intervention
  • Identify the outcomes the person hopes for
  • Create an agreement/contract about what
    outcomes are attainable
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3
Q

What are the consensus guidelines for assessment? (Brundage et al, 2021)

A
  • Stuttering related background
    information
  • Speech, language ,
    Temperament, and related
    background information
  • Speech Fluency and Stuttering
    behaviour
  • Speaker’s reactions to
    stuttering
  • Reactions to stuttering within
    the Environment
  • Adverse Impact associated
    with Stuttering
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4
Q

ICF (International Classification of Functioning and Health - Yaruss & Quesal, 2004)

A
  • Shift towards creating a distinction between aetiology and consequences
  • Distinction between cause and results
  • Impact on daily life
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5
Q

Reducing Negative Reactions (Murphy and Yaruss, 2007):

A
  • Strategies to overcome children’s negative reactions to their stuttering
  • Talking about thoughts and feelings about stuttering
  • Understanding the nature of the problem
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6
Q

OASES (Overall Assessment of the Speaker’s Experience of Stuttering - Yaruss & Quesal, 2006)

A
  • Quality of lifw
  • Thoughts and feelings behind stutter
  • Focuses on the speaker’s experience of stuttering as defined by the ICF
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7
Q

WASSP (Wright-Ayre Stuttering Self-Rating Profile):

A

Based on the ICF framework
Understand how individuals who stutter see and feel about their stuttering
How they avoid certain speaking situations
Whether they feel like stuttering puts them at a disadvantage in any way
Their personal feelings and perspectives on stutterin

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8
Q

Observations during Assessment:

A
  • Frequency of stuttering is most commonly reported as % of syllables stuttered
  • Variety of samples, ideally video with written consent
  • Average the duration of the 3 longest stutters in a sample
  • Secondary behaviors: physical movements/extra sounds/pitch rise
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9
Q

Discrepancies:

A
  • Disagreements between people who stutter, professionals, and authorities on what constitutes stuttering
  • Research into outcomes has focused on quantifiable behaviors
  • Consistency in measuring stuttering events is essential
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10
Q

Persistence and Recovery:

A

Rates of recovery differ across studies
- recovery occurs between the ages of two and half and four and a half years (Bernstein Ratner,
2010)
- spontaneous recovery may
occur up to five years post onset (Baxter, 2015; Bernstein
Ratner, 2005; Curlee & Yairi, 1997; Blomgren, 2013).

Approximately 70-80% of children who begin to stutter will spontaneously recover
Factors influencing persistence and recovery

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11
Q

Predicting persistence and recovery

A

Walsh et al (2018)
Provide supplemental evidence of the role of known predictive
factors (e.g., sex and family history of persistent stuttering).
Provide evidence that
*early delays in basic speech motor processes (especially in boys),
* poor performance on a non word repetition test,
*stuttering severity at the age of 4 to 5 years,
*and delayed or atypical functioning in central nervous system
language processing networks are predictive of persistent
stuttering.

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12
Q

Onset, development and recovery

A

Longitudinal study by Yairi & Ambrose (2005)

  • Identifies cognitive abilities for CWS are no different to CWNS
  • Expressive language skills are average or above average close
    to onset, although children who persist in stuttering tend to be
    slower in phonological development than those who recover
  • Approximately 70-80% of children who begin to stutter will
    spontaneously recover from symptoms within one to two
    years post-onset (Bernstein Ratner, 2005; Curlee & Yairi,
    1997)
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13
Q

What are you assessing?

A
  • Family history of stuttering
  • Language development
  • Phonological development
  • Motor development
  • Temperament
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14
Q

Assessing feelings and attitudes:

A
  • The need to work with the whole person
  • Instruments such as OASES and WAASP
  • The impact of self-stigma on self-esteem and self-efficacy
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15
Q

Key elements in Assessment/Therapy?

A
  • Identification
  • Desensitization
  • Stigma and Stereotyping
  • The importance of addressing the whole person
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16
Q

Goals of assessment may include:

A

Assessing confidence and participation in communication
Understanding self-perception as a communicator
Evaluating support systems
Gathering input from various sources
Handling questions, teasing, bullying, and reactions when talking

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17
Q

Behaviours to assess:

A
  • Avoidance: the degree to which the PWS
    successfully use avoidance behaviours in order
    to give the appearance of a person with mild or
    even no stuttering
  • Postponement: as the PWS approaches a
    feared word there is often a moment of
    hesitation or the speaker may use a serious of
    sounds e.g. um/ah/let me see/you know
  • Substitution: substitution of words
  • Loss of control: speaker identifies
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18
Q

Normal non fluency vs stuttering

A

Normal non fluency:
- part/whole word repetitions (<3)
- phrase repetitions
- single syllable word repetitions

Stuttering:
- Part/whole word repetitions (>3)
- Phoneme/syllable repetitions
- prolongations/blocks
- tension
- incresed awareness
- secondary behaviours

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19
Q

When might stuttering be more likely to persist?

A
  • Family history of persistent stuttering
  • Relatives continue to stutter
  • Male
  • Stable or increasing number of SLDs (stutter-like dysfluencies) within one year of
    onset
  • Stable or increasing severity rating by parents/clinicians
  • Few repetitions (more blocks and prolongations than reps)
  • Strong reactions to stuttering by parents/child
  • Later onset of stuttering (4 years up)
  • Concomitant (co-occurring) learning or communication problems
20
Q

When is stuttering less likely to persist? (Manning, 2010)

A
  • No relatives who stutter
  • Female
  • Within one year of onset
  • Decreasing pattern of SLDs within one year of
    onset
  • Few reactions to stuttering by child or parents
  • Early onset of stuttering (2-3 years)
  • Decreasing severity ratings by parents and
    clinicins
21
Q

Cluttering severity instrument

A

Eight dimensions:
1. Overall intelligibility
2. Speech rate regularity
3. Speech rate
4. Articulatory precision
5. Typical disfluency
6. Language disorganisation
7. Discourse management
8. Use of prosody (tone and rhythm)

22
Q

Cluttering Assessment

A
  • Monologue
  • Reading
  • Story retelling

a person who stutters doesn’t slow down their speech for the more complicated parts, which leads to more typical speech difficulties like repeating words or phrases and making sentence structure mistakes. (Van Zaalen, 2009)

6.4 times more normal disfluencies in
spontaneous speech and retelling

  • Speech motor coordination (10 repetitions of
    puhtukkuh) judging articulatory accuracy and
    smooth flow (co-articulation, flow and sequencing)
    and rate
  • Skills in oral motor coordination in multisyllabic
    words (Van Zaalen, 2009)
23
Q

Evidence-Based Practice (EBP) in Speech-Language Pathology:

A

EBP emphasizes the importance of clinicians documenting intervention results and choosing treatment approaches based on a substantial body of literature. This is particularly relevant in the field of fluency disorders.

24
Q

Stuttering as More Than Surface Features:

A

Stuttering involves not only observable behaviors but also intrinsic aspects that profoundly affect individuals. These “under the surface” aspects include emotional reactions, cognitive responses, and the overall impact on a person’s life.

25
Q

Sheehan’s “Iceberg” Analogy:

A

Sheehan’s analogy illustrates that much of the experience of stuttering occurs below the surface, encompassing more than just observable speech disfluencies.

26
Q

Challenges in Studying Intrinsic Aspects of Stuttering:

A

Research on the less-observable components of stuttering is limited. Various factors may contribute to this gap, such as the difficulty of defining and measuring intrinsic aspects and skepticism regarding their significance.

27
Q

Need for Comprehensive Treatment Outcomes Research:

A

There is a pressing need for research on the outcomes of treatment that extends beyond the surface speech behaviors to address the full scope of the stuttering disorder.

28
Q

Measurement of Intrinsic Aspects:

A

Instruments for measuring less-observable components of stuttering exist, but they have not been widely used in treatment outcomes research. These instruments can provide insights into a speaker’s fluency, confidence, emotional reactions, attitudes, and more.

29
Q

clinical implications of OASES

A

Clinicians should recognize that the effects of stuttering extend beyond the observable behaviors and consider the intrinsic aspects of the disorder.

Utilizing instruments like the OASES can help clinicians and researchers comprehensively assess the experiences and outcomes of stuttering treatment.

A broader understanding of stuttering and its impact on individuals can guide evidence-based practice, enabling more informed treatment decisions and improving the overall quality of care

30
Q

Initial Trial Instruments: SRS, FCS, and QOL-S

A

The OASES consists of three initial trial instruments designed to target specific components of the stuttering disorder defined by the WHO model.
These components include the speaker’s reactions to stuttering (SRS), functional communication and stuttering (FCS), and quality of life and stuttering (QOL-S).

31
Q

Speaker’s Reactions to Stuttering (SRS)

A

SRS was designed to gather information about how speakers felt about their speech, the actions they engaged in due to stuttering, and their thoughts and perceptions about communication difficulties.
The SRS addressed affective, behavioral, and cognitive reactions, including negative emotions like embarrassment and anxiety.
Focus groups and specialists provided input to refine the SRS, which initially contained 100 items.

32
Q

Functional Communication and Stuttering (FCS)

A

FCS focused on the disability of stuttering and the impact of the environment on communication by examining difficulties in relevant life situations.
It contained 35 items and examined challenges in general communication, work-related communication, and social interaction.
Input from focus groups and specialists was used to refine the FCS

33
Q

Quality of Life and Stuttering (QOL-S)

A

QOL-S assessed the potential disadvantages experienced due to stuttering, including its impact on overall quality of life.
It included 30 items and was based on items from other quality of life instruments but modified for stuttering.
Focus groups and specialist reviews were used for refinement.

34
Q

Initial Pilot Studies: Item Analysis

A

The early drafts of SRS, FCS, and QOL-S were tested in two pilot studies, involving participant feedback and analysis.
Item distributions were analyzed to avoid floor or ceiling effects and ensure appropriate variability.
Pairwise correlations were conducted to eliminate redundant items and maintain reliability.

35
Q

Initial Pilot Studies: Validity and Reliability

A

The S-24 was used for concurrent validity assessment.
Content validity was ensured through focus groups, participant feedback, and specialist input.
Preliminary test-retest reliability was assessed, with the majority of items showing high reliability.

36
Q

First Integrated Instrument: CASES

A

The three initial instruments (SRS, FCS, QOL-S) were combined into CASES to address the WHO’s ICF framework and WHO terminology.
A general information section was added, making it a “Comprehensive Assessment of the Speaker’s Experience of Stuttering” (CASES) instrument.

37
Q

Additional Pilot Analyses and Final Revisions

A

A larger sample was used for further pilot analyses, involving a broad cross-section of people who stutter.
Data quality checks were performed, and sections with incomplete or uniform responses were excluded.
Detailed item analyses were conducted for item distributions, correlations, and internal reliability.
The resulting integrated instrument was named OASES, with minor wording changes.

38
Q

OASES contains:

A

General Information (Section I):
Reactions to Stuttering (Section II):
Communication in Daily Situations (Section III):
Quality of Life (Section IV):

39
Q

General Information

A

Focuses on the speaker’s perceived fluency and speech naturalness.
Assesses the speaker’s knowledge about stuttering and stuttering therapy.
Explores overall perceptions about stuttering.

40
Q

Reactions to Stuttering

A

Examines the speaker’s affective, behavioral, and cognitive reactions to stuttering.
Evaluates how the speaker responds emotionally and behaviorally to stuttering experiences.

41
Q

Communication in Daily Situations

A

Assesses the degree of difficulty speakers have when communicating in various situations, including work, social settings, and home.
Focuses on communication difficulties rather than fluency in these situations.

42
Q

Quality of Life

A

Focuses on how much stuttering interferes with the speaker’s satisfaction with their ability to communicate, relationships, ability to participate in their lives, and overall well-being.

43
Q

Scoring procedures for OASES

A

Response scales are organized so that higher scores indicate a greater degree of negative impact associated with stuttering.
Scores are based on the calculation of an “impact score,” which involves the ratio of the total number of points in the respondent’s answers to the total number of possible points for the items that were completed.
Impact scores range from a minimum of 20 to a maximum of 100, regardless of the number of items a speaker might skip

44
Q

Impact ratings of OASES

A

Impact ratings are analogous to traditional severity ratings and provide an indication of the impact of stuttering.
The impact scores are divided into different categories representing varying degrees of stuttering impact: mild, mild-to-moderate, moderate, moderate-to-severe, and severe

45
Q

Final Evaluation of Reliability of OASES

A

Test-retest reliability was examined by distributing the OASES to 20 adults who stutter, with 14 of them completing the instrument on two occasions separated by 10-14 days.
Point-to-point agreement for individual items was high, with strong consistency between test administrations.
Impact scores showed a high degree of test-retest reliability, with Pearson product–moment correlations ranging from 0.90 to 0.97.
Impact ratings remained stable between the first and second administrations of the instrument, confirming strong reliability.

46
Q

What is the Palin PRS?

A

It is designed for parents or guardians to rate their child’s therapy sessions.
Parents use a 0-10 scale to rate nineteen statements.
Provides valuable insights into the parent or guardian’s viewpoint on their child’s stammering therapy.
It is used by The Michael Palin Centre and their therapists.
The measure was created at The Michael Palin Centre using a Delphi approach. Parents of children who stammer were involved in defining important therapy outcomes. Statements rated highly by a majority of respondents were incorporated into the Palin PRS.
Over time, data has been collected to assess the validity, internal reliability, component factors, and normative scores of the Palin PRS.

47
Q
A