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Göteborgs universitets publikationer

Assessment of data quality in a multi-centre cross-sectional study of participation and quality of life of children with cerebral palsy

Författare och institution:
H. Dickinson (-); K. Parkinson (-); V. McManus (-); C. Arnaud (-); Eva Beckung (Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa); J. Fauconnier (-); S. I. Michelsen (-); J. Parkes (-); G. Schirripa (-); U. Thyen (-); A. Colver (-)
Publicerad i:
BMC Public Health, 6 s. 273
1471-2458 (Electronic)
Artikel, refereegranskad vetenskaplig
Sammanfattning (abstract):
BACKGROUND: SPARCLE is a cross-sectional survey in nine European regions, examining the relationship of the environment of children with cerebral palsy to their participation and quality of life. The objective of this report is to assess data quality, in particular heterogeneity between regions, family and item non-response and potential for bias. METHODS: 1,174 children aged 8-12 years were selected from eight population-based registers of children with cerebral palsy; one further centre recruited 75 children from multiple sources. Families were visited by trained researchers who administered psychometric questionnaires. Logistic regression was used to assess factors related to family non-response and self-completion of questionnaires by children. RESULTS: 431/1,174 (37%) families identified from registers did not respond: 146 (12%) were not traced; of the 1,028 traced families, 250 (24%) declined to participate and 35 (3%) were not approached. Families whose disabled children could walk unaided were more likely to decline to participate. 818 children entered the study of which 500 (61%) self-reported their quality of life; children with low IQ, seizures or inability to walk were less likely to self-report. There was substantial heterogeneity between regions in response rates and socio-demographic characteristics of families but not in age or gender of children. Item non-response was 2% for children and ranged from 0.4% to 5% for questionnaires completed by parents. CONCLUSION: While the proportion of untraced families was higher than in similar surveys, the refusal rate was comparable. To reduce bias, all analyses should allow for region, walking ability, age and socio-demographic characteristics. The 75 children in the region without a population based register are unlikely to introduce bias.
Ämne (baseras på Högskoleverkets indelning av forskningsämnen):
Bias (Epidemiology), Cerebral Palsy/physiopathology/*psychology, Child, Cross-Sectional Studies, Disabled Children/*psychology, Europe, Family/psychology, Female, Humans, Logistic Models, Male, Psychometrics, *Quality of Life, Questionnaires, Registries, Research Design, *Sickness Impact Profile, *Social Environment, Social Support, Walking/physiology
Postens nummer:
Posten skapad:
2007-10-15 14:54
Posten ändrad:
2011-01-20 09:58

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