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Self-reports versus parental perceptions of health-related quality of life among deaf children and adolescents
dc.contributor.author | Pardo-Guijarro M.J. | |
dc.contributor.author | Martínez-Andrés M. | |
dc.contributor.author | Notario-Pacheco B. | |
dc.contributor.author | Solera-Martínez M. | |
dc.contributor.author | Sánchez-López M. | |
dc.contributor.author | Martínez-Vizcaíno V. | |
dc.date.accessioned | 2020-09-02T22:25:20Z | |
dc.date.available | 2020-09-02T22:25:20Z | |
dc.date.issued | 2014 | |
dc.identifier | 10.1093/deafed/env018 | |
dc.identifier.citation | 20, 3, 275-282 | |
dc.identifier.issn | 10814159 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12728/5746 | |
dc.description | The aim of this study was to assess the agreement between deaf children's and adolescents' self-ratings of health-related quality of life (HRQoL) and their parents' proxy reports. This observational cross-sectional study included 114 deaf 8-to 18-years-old students and proxy family members. HRQoL was measured using the KIDSCREEN-27 questionnaire, which was adapted to Spanish sign language for children, with a written version for parents. Respondents completed a selfadministered paper questionnaire. Parents' and children's mean scores differences were not significant, except for the "Autonomy and Parents" and "Peers and Social Support" dimensions. Children aged 8-11 years scored higher in some domains of QoL compared to those aged 12-18 years. The level of agreement between children/adolescents' and parents/proxies' responses was acceptable, except for the dimension "Autonomy and Parents." Overall, deaf children/adolescents' self-ratings of HRQoL did not differ from their parents' proxy reports; however, differences were found in the dimensions that explored the quality of the interaction of children/adolescents and parents, the perceived level of autonomy, and social relations and support. © The Author 2015. Published by Oxford University Press. All rights reserved. | |
dc.language.iso | en | |
dc.publisher | Oxford University Press | |
dc.title | Self-reports versus parental perceptions of health-related quality of life among deaf children and adolescents | |
dc.type | Article |