Reliability of the Luganda version of the Child Behaviour Checklist in measuring behavioural problems after cerebral malaria

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Date
2009-12-08Author
Bangirana, Paul
Nakasujja, Noeline
Giordani, Bruno
Opoka, Robert O.
Chandy, C. John
Boivin, Michael J.
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Background: No measure of childhood behaviour has been validated in Uganda despite the
documented risks to behaviour. Cerebral malaria in children poses a great risk to their behaviour,
however behavioural outcomes after cerebral malaria have not been described in children. This
study examined the reliability of the Luganda version of the Child Behaviour Checklist (CBCL) and
described the behavioural outcomes of cerebral malaria in Ugandan children.
Methods: The CBCL was administered to parents of 64 children aged 7 to 16 years participating
in a trial to improve cognitive functioning after cerebral malaria. These children were assigned to
the treatment or control group. The CBCL parent ratings were completed for the children at
baseline and nine weeks later. The CBCL was translated into Luganda, a local language, prior to its
use. Baseline scores were used to calculate internal consistency using Cronbach Alpha.
Correlations between the first and second scores of the control group were used to determine
test-retest reliability. Multicultural norms for the CBCL were used to identify children with
behavioural problems of clinical significance.
Results: The test-retest reliability and internal consistency of the Internalising scales were 0.64 and
0.66 respectively; 0.74 and 0.78 for the Externalising scale and 0.67 and 0.83 for Total Problems.
Withdrawn/Depressed (15.6%), Thought Problems (12.5%), Aggressive Behaviour (9.4%) and
Oppositional Defiant Behaviour (9.4%) were the commonly reported problems.
Conclusion: The Luganda version of the CBCL is a fairly reliable measure of behavioural problems
in Ugandan children. Depressive and thought problems are likely behavioural outcomes of cerebral
malaria in children. Further work in children with psychiatric diagnoses is required to test its validity in a clinical setting.
URI
http://www.capmh.com/content/3/1/38http://dx.doi.org/10.1186/1753-2000-3-38
http://hdl.handle.net/10570/531