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Psychometric properties of the Quality of Life Questionnaire for Children with CP

dc.contributor.authorWaters, Elizabeth
dc.contributor.authorDavis, Elise
dc.contributor.authorMackinnon, Andrew
dc.contributor.authorBoyd, Roslyn
dc.contributor.authorGraham, H.Kerr
dc.contributor.authorLo, Sing Kai
dc.contributor.authorWolfe, Rory
dc.contributor.authorStevenson , Richard D
dc.contributor.authorBjornson, Kristie
dc.contributor.authorBlair, Eve
dc.contributor.authorHoare, Peter
dc.contributor.authorRavens-Sieberer, Ulrike
dc.contributor.authorReddihough, Dinah
dc.date.accessioned2015-12-08T22:27:15Z
dc.date.issued2007
dc.date.updated2015-12-08T09:18:06Z
dc.description.abstractThis paper describes the development and psychometric properties of a condition-specific quality of life instrument for children with cerebral palsy (CP QOL-Child). A sample of 205 primary caregivers of children with CP aged 4 to 12 years (mean 8y 5mo) and 53 children aged 9 to 12 years completed the CP QOL-Child. The children (112 males, 93 females) were sampled across Gross Motor Function Classification System (GMFCS) levels (Level I=18%, II=28%, III=14%, IV=11%, V=27%). Primary caregivers also completed other measures of child health (Child Health Questionnaire; CHQ), QOL (KIDSCREEN), and functioning (GMFCS). Internal consistency ranged from 0.74 to 0.92 for primary caregivers and from 0.80 to 0.90 for child self-report. For primary caregivers, 2-week test-retest reliability ranged from 0.76 to 0.89. The validity of the CP QOL is supported by the pattern of correlations between CP QOL-Child scales with the CHQ, KIDSCREEN, and GMFCS. Preliminary statistics suggest that the child self-report questionnaire has acceptable psychometric properties. The questionnaire can be freely accessed at http://www.deakin.edu.ac/hmnbs/chase/cerebralpalsy/cp_qol_home.php.
dc.identifier.issn0012-1622
dc.identifier.urihttp://hdl.handle.net/1885/33997
dc.publisherMac Keith Press
dc.sourceDevelopmental Medicine and Child Neurology
dc.subjectKeywords: article; cerebral palsy; child; female; hospitalization; human; male; pathophysiology; preschool child; psychological aspect; psychometry; quality of life; questionnaire; reproducibility; validation study; caregiver; child health; classification; controll
dc.titlePsychometric properties of the Quality of Life Questionnaire for Children with CP
dc.typeJournal article
local.bibliographicCitation.lastpage55
local.bibliographicCitation.startpage49
local.contributor.affiliationWaters, Elizabeth, Deakin University
local.contributor.affiliationDavis, Elise, Deakin University
local.contributor.affiliationMackinnon, Andrew, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationBoyd, Roslyn, Murdoch Children's Research Institute
local.contributor.affiliationGraham, H.Kerr, University of Melbourne
local.contributor.affiliationLo, Sing Kai, Deakin University
local.contributor.affiliationWolfe, Rory, Monash University
local.contributor.affiliationStevenson , Richard D, University of Virginia
local.contributor.affiliationBjornson, Kristie, Children's Hospital and Regional Medical Center
local.contributor.affiliationBlair, Eve, University of Western Australia
local.contributor.affiliationHoare, Peter, Royal Hospital for Sick Children
local.contributor.affiliationRavens-Sieberer, Ulrike, Robert Koch Institute
local.contributor.affiliationReddihough, Dinah, Royal Children's Hospital Melbourne (University of Melbourne)
local.contributor.authoruidMackinnon, Andrew, u4231647
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor111714 - Mental Health
local.identifier.absseo920410 - Mental Health
local.identifier.ariespublicationU4146231xPUB108
local.identifier.citationvolume49
local.identifier.doi10.1017/S0012162207000126.x
local.identifier.scopusID2-s2.0-33847011039
local.type.statusPublished Version

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