Rice 2017
Rice 2017
Brief Report
© 2017 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and
John Wiley & Sons Ltd
Journal of Intellectual Disability Research
2
L. J. Rice et al. • Concurrence of the SDQ and DBC
where it is important to focus on behavioural profiles The Developmental Behaviour Checklist primary
in children with ID, a specialised ID instrument with carer version (DBC-P; Einfeld & Tonge, 2002;
established psychometric properties, such as the Einfeld et al., 2006; Tonge & Einfeld, 2003) was
DBC-P, may provide more reliable and valid specifically developed for young people with ID aged
information. 4–18 years, and is designed to measure a broad range
of emotional and behavioural problems. The DBC-P
Keywords concurrent validity, developmental
has five factor analytically derived sub-scales
behaviour checklist, intellectual disability, strength
producing a behavioural profile. The total scale score
and difficulties questionnaire
includes a clinical cut-off score, derived from a
Receiver Operating Characteristics (ROC) analysis,
The present investigation arose from the concurrence to differentiate between individuals with and without
of two studies, the Longitudinal Study of Australian clinically significant emotional and behavioural
Children (LSAC), a population study (Gray & Smart, problems. It can also be used as a repeated measure to
2009; Bayer et al., 2011) and the Stepping Stones monitor intervention effectiveness. The DBC-P cut-
Triple P (SSTP) Project, a public health community off has high agreement with clinical diagnosis (Einfeld
intervention for parents of children with & Tonge, 2002).
developmental disabilities aged 2–12 years (Tellegen The aim of this study was to estimate the
& Sanders, 2013). To assess behavioural disturbance, relationship between DBC-P and SDQ scores in the
the LSAC used the Strengths and Difficulties context of children with ID, (1) as a continuous
Questionnaire (SDQ), a measure designed for measure and (2) as a binary classifier registering
typically developing children; the SSTP project uses behaviour indicative of psychopathology. We
the Developmental Behaviour Checklist – Parent examined the concurrent validity of scores on the
version (DBC-P), a measure specifically for children DBC-P and SDQ as well as the positive, negative and
with disabilities. To assess the representativeness of overall agreement between DBC-P and SDQ cut-offs.
children receiving SSTP, it was necessary to compare High correlations between scores on the two
their level of behaviour problems with that of the measures as well as high agreement between the cut-
Australian LSAC intellectual disability (ID) offs would support the use of the SDQ in research
population. As a preliminary to this, our aim in the with children with ID.
present study was to estimate the relationship between
the SDQ and the DBC-P in children with ID.
The SDG (Goodman, 1997) is a widely used Method
measure of psychological well-being in children and
adolescents aged 4–17 years. It is cited in over 6000
publications and translated into almost a hundred
Participants
languages. It has high concurrent validity with other Eighty-three parents of children with ID (55 males, 29
measures of behavioural problems in typically females; mean age 10.8 years, SD 3.0, range 4–17)
developing children, including the Child Behaviour participated. Thirty-four participants (40%) were
Checklist (Goodman & Scott, 1999; Muris et al., recruited through two mental health service clinics in
2003) and the Rutter Parent and Teacher Australia (clinic group; 23 males, 11 females; mean
Questionnaire (Goodman, 1997). Although designed age 9.4 years, SD 2.8, range 5–15 years); the remain-
for typically developing children, there is some der (50; 60%) were recruited from a large-scale survey
evidence that the SDQ may also be suitable for of children with Down syndrome in England and
young people with ID. In both typically developing Wales (Down syndrome group; 32 males, 18 females;
and ID groups, inter-rater agreements between mean age 11.8 years, SD 2.8, range 8–17 years). In
parent, teacher and child reports are similar (Beck total, 50 (60%) participants had Down Syndrome; 28
et al., 2004; Emerson, 2005; Kaptein et al., 2008). (33%) had a diagnosis of Autism Spectrum Disorder;
The pattern of child self-reported SDQ scores is also 5 (6%) had other disorders (Prader-Willi syndrome,
consistent with ICD-10 psychiatric diagnoses in Costello syndrome, Tetrasomy 18p, global develop-
children with ID (Emerson, 2003, 2005). mental delay, cerebral palsy).
© 2017 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and
John Wiley & Sons Ltd
Journal of Intellectual Disability Research
3
L. J. Rice et al. • Concurrence of the SDQ and DBC
© 2017 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and
John Wiley & Sons Ltd
Journal of Intellectual Disability Research
4
L. J. Rice et al. • Concurrence of the SDQ and DBC
Table 1 DBC-P and SDQ total raw score and sub-scale raw scores
Down syndrome group Mean (SD) Clinic group Mean (SD) Combined Mean (SD)
(N = 50) (N = 34) (N = 84)
DBC-P, Developmental Behaviour Checklist – Parent version; SDQ, Strengths and Difficulties Questionnaire.
© 2017 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and
John Wiley & Sons Ltd
Journal of Intellectual Disability Research
5
L. J. Rice et al. • Concurrence of the SDQ and DBC
Table 3 Proportions of participants scoring above and below the DBC-P and SDQ cut-offs
Down syndrome
Below cut-off 28 (56%) 28 (56%) 37 (74%)
Above cut-off 22 (44%) 22 (44%) 13 (26%)
2 2
McNemar’s Test Χ (1) = 0.00, P = 1 Χ (1) = 5.40, P = 0.002
Clinic sample
Below cut-off 6 (18%) 4 (12%) 8 (24%)
Above cut-off 28 (82%) 30 (88%) 26 (76%)
2 2
McNemar’s Test Χ (1) = 1, P = 0.32 Χ (1) = 0.67, P = 0.41
Combined
Below cut-off 34 (40%) 32 (38%) 45 (54%)
Above cut-off 50 (60%) 52 (62%) 39 (46%)
2 2
McNemar’s Test Χ (1) = 0.29, P = 0.59 Χ (1) = 5.76, P = 0.02
The study has several limitations. Data are based and specificity for detecting differences between
on convenience samples involving mainly children individuals with and without clinically significant
with Down syndrome and autism, and although all emotional and behavioural problems unknown. Other
were classified as having ID, details of intellectual important psychometric properties for children with
functioning were not available. The samples were also ID, for example, sensitivity to change and inter-rater
recruited from very different sources, with the clinic agreement, are also missing. Thus, where it is
group, as expected having higher levels of behaviour important to focus on behavioural profiles in children
problems than the survey group. However, this with ID, as in the SSTP Project (Tellegen & Sanders,
provided a wide range of levels of 2013), the DBC-P may be preferable. The DBC-P is
emotional/behavioural problems, and the association also likely to be more informative in clinical settings
between the DBC-P and the SDQ borderline score when these features are particularly important
was confirmed in both cohorts. In the Down (Chandler et al., 2016).
syndrome group, there was also a delay between
parents’ completing the SDQ and the DBC-P, which
Conflict of Interest
may have reduced the agreement between scores on
the two measures. Finally, there was no direct Professor Einfeld and Emeritus Professor Tonge are
assessment of the children’ s behavioural and mental the authors of the Developmental Behaviour
state and the lack of comparison with clinical Checklist. They receive royalties for the German
psychiatric diagnoses for the SDQ, and the language version but derive no personal or financial
concurrent direct psychiatric diagnosis and DBC-P benefit from the sale of any of other versions. No
data are derived from a previous study (Einfeld & other authors reported any financial disclosures.
Tonge, 1995).
Despite these caveats, our findings suggest that in
epidemiological studies such as the LSAC population
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© 2017 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and
John Wiley & Sons Ltd
Journal of Intellectual Disability Research
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© 2017 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and
John Wiley & Sons Ltd