2015
DOI: 10.1016/j.yebeh.2015.06.023
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Cross-cultural adaptation of the Malay version of the child self-report Health-related Quality of Life Measure for Children with Epilepsy (CHEQOL-25) in Malaysia

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Cited by 4 publications
(3 citation statements)
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“…The subsequent layers consist of extended family, other friends and acquaintances. For CWE, due to the isolation and stigma they may face, it is not surprising most had a small circle, but as the number grew there was a benefit to their QoL as has been shown in other studies [10].…”
Section: Cwe Having More Friendsmentioning
confidence: 55%
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“…The subsequent layers consist of extended family, other friends and acquaintances. For CWE, due to the isolation and stigma they may face, it is not surprising most had a small circle, but as the number grew there was a benefit to their QoL as has been shown in other studies [10].…”
Section: Cwe Having More Friendsmentioning
confidence: 55%
“…There have been very few studies about QoL in CWE in sub-Saharan Africa [7,8] including in Kenya where there are mostly qualitative studies and focusing on stigma [9]. The CHEQOL-25 tool has been used in other developing countries, where cross-cultural transferability, testretest reliability, and internal consistency have all been well demonstrated [10]. There is no published data on the use of the tool in sub-Saharan Africa.…”
Section: Introductionmentioning
confidence: 99%
“…The QoL of children with epilepsy after surgery was assessed using the CHEQOL-25 scale, a QoL assessment tool proposed by Gabriel Ronen, which evaluated five aspects of epilepsy: “Present Concerns,” “Interpersonal Emotion,” “Secrecy,” “Normality,” and “Future Worries.” Subjects responded to five questions for each aspect and a total percentage score for each item was calculated, with higher scores representing a better QoL ( 17 ). The CHEQOL-25 scale is being used in children with epilepsy postoperatively in some developing countries in Southeast Asia ( 18 ). The questionnaire is designed to be filled out either by the children or by the caregivers, but, as the children in the present study had seizures, we elected to have the questionnaire filled out by the caregivers.…”
Section: Methodsmentioning
confidence: 99%