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78

JCPSLP

Volume 19, Number 2 2017

Journal of Clinical Practice in Speech-Language Pathology

and child–parent pairs should not have extra demands

placed on them that were not contingent with standard LP

treatment. Children entered treatment at different points

due to the “rolling” nature of the groups, some towards

the end of the research protocol timeframe. Children who

moved from Stage 1 to Stage 2 were seen individually at

three sites and within a Stage 2 group at one site. Where

possible the post-commencement assessments were

integrated into Stage 1 or Stage 2 sessions. As such there

is variation in numbers of clients at the 6- and 9-months

post-commencement assessments. O’Brian et al. (2013)

experienced similar variation in their translational study

at the 9-months post-treatment assessment due to

withdrawals (21%), Stage 1 completers (65%), and those

still in Stage 1 (14%).

Outcomes

Measurements of stuttering severity were collected for all

available children at the 6 months post-commencement (n

= 14) and 9 months post-commencement (n = 10)

assessments. Baseline characteristics for all 19 children

who commenced the study groups are shown in Table 1.

There was no significant difference at baseline between

those who completed to Stage 1 and those who withdrew

from treatment.

paediatric sample of stuttering. The eight SLPs rated this

sample using the SR scale. All SR scores were within one

point, demonstrating rater consistency as per the LP

guidelines. Each clinician’s clinical hours per child to the

completion of Stage 1 were calculated by dividing the

minutes taken for each group by the number of children

(Arnott et al., 2014). Number of clinic visits and weeks per

child to completion of Stage 1 included all attended group

sessions, other than the initial parent training session (PTS).

Direct treatment did not begin until after the groups had

commenced. As such, the PTS was deemed part of the

assessment and planning stage, in line with multiple

assessment sessions as seen within stuttering research

(Franken, Kielstra-Van der Schalk, & Boelens, 2005;

McCulloch, Swift, & Wagnitz, 2017). The number of weeks

was calculated from the date of each child’s first

attendance to the date of the last group in which criteria for

Stage 2 was met.

Generalised estimating equation method (GEE) for

a normally distributed outcome was used to analyse

%SS and SR for the repeated assessment times of

pre-treatment (T1), 6 months (T2) and 9 months (T3)

post-commencement. Analysis was by intention to treat,

where all participants commencing the program were

included, resulting in analyses of 19 participants. The

GEE method enables participants with missing data at

the 6- or 9-month assessment times to be retained in the

analysis. Assessment times were clustered by participant

and an exchangeable covariance structure was assumed

which is equivalent to the compound symmetry structure

used in a repeated measures analysis of variance. The

within-participant factor for time was assessed and its two

components T1 with T2 and T2 with T3.

An independent

t

-test was used to compare those who

completed to Stage 1 against those who withdrew from

treatment, on variables of age, stuttering severity (%SS &

SR). Differences between those who completed to Stage

1 and those who withdrew from treatment in terms of

gender were assessed using a chi-square test. All analysis

was conducted using SPSS (v. 22) statistical software with

statistical significance defined as p-value < 0.05.

Results

Attrition

Twenty-one children enrolled in the study; however, two

children withdrew prior to attending groups. The data from

the remaining 19 children was included for analysis. Twelve

participants completed Stage 1 and seven did not

complete Stage 1. Reasons for not completing Stage 1 and

early withdrawal (n = 2) prior to group commencement

included parental uncertainty about the treatment (n = 1),

prioritising other areas of treatment such as speech sound

disorders (n = 1), moving out of area (n = 1), failure to

contact the service after missed sessions thereby activating

discharge policy (n = 1), maternal health (n = 1), balancing

siblings needs (n = 1) and continuing with ongoing

stuttering treatment as the criteria for Stage 2 had not been

met within the time frame of the research (n = 3). Factors

leading to non-completion of Stage 1 and/or withdrawal

from the present study and the percentage of participants

(37%) are in line with other stuttering treatment studies

(McCulloch et al., 2017; Trajkovski et al., 2011).

It was beyond the remit of this clinician-led community

study to carry out ongoing follow-up to monitor long-term

treatment outcomes. In line with the real-world ethos

underpinning the design was that participating SLPs

Table 1. Baseline assessment information for

children who commenced rolling-group therapy

Characteristics

Commenced

Completed

Stage 1

Gender n (%)

Boy

Girl

7 (36.8)

12 (63.2)

7 (58.3)

5 (41.7)

Age (years;months)

< 3;5

3;5 – 4;5

> 4;5

3 (15.8)

10 (52.6)

6 (31.6)

1 (8.3)

6 (50.0)

5 (41.7)

Mean age in months (SD)

49.05 (7.9)

50.58 (8.1)

Mean %SS pre-treatment (SD)

7.39 (3.9)

6.02 (5.2)

Mean SR pre-treatment (SD)

5.26 (1.6)

5.0 (1.7)

The mean number of SLP hours per child to complete

Stage 1 was 7.3 clinical hours (SD = 2.7, range = 2.69–11.58).

The median number of clinic visits to the completion of

Stage 1 was 15 visits (interquartile range 12.3). The

interquartile range values show that 75% of the children

completed Stage 1 within 23 visits. The median number of

weeks to complete Stage 1 was 27 (interquartile range 19.2),

with 75% of the children reaching Stage 2 within 34.7 weeks.

The mean %SS score at the completion of Stage 1

for the entire sample (n = 12) was 0.37 %SS (SD = 0.38

Range = 0.00–0.98). Measures of %SS and SR at initial

assessment, 6 months post-commencement and 9 months

post-commencement showed a trajectory towards little or

no stuttering across the treatment period (Table 2, figures 1

and 2). Children (n = 10) who were assessed at 9 months

post-commencement of treatment scored a mean %SS of

1.3 %SS (SD = 2.1; Range = 0–5.3), while the subset of

those who had completed Stage 1 (n = 7) scored a mean

%SS of 0.9%SS (SD = 1.9; Range = 0–5.3). The downward

trend was similar for both those who completed Stage 1

and those who were continuing in treatment.