Literature DB >> 18571944

Frequency of participation of 8-12-year-old children with cerebral palsy: a multi-centre cross-sectional European study.

Susan I Michelsen1, Esben M Flachs, Peter Uldall, Eva L Eriksen, Vicki McManus, Jackie Parkes, Kathryn N Parkinson, Ute Thyen, Catherine Arnaud, Eva Beckung, Heather O Dickinson, Jérôme Fauconnier, Marco Marcelli, Allan Colver.   

Abstract

Participation in home, school and community is important for all children; and little is known about the frequency of participation of disabled children. Frequency of participation is a valuable outcome measure for evaluating habilitation programmes for disabled children and for planning social and health services. We investigated how frequency of participation varied between children with cerebral palsy and the general population; and examined variation across countries to understand better how the environmental factors such as legislation, public attitudes and regulation in different countries might influence participation. We undertook a multi-centre, population-based study in children with and without cerebral palsy. Working from the Life-H instrument, we developed a questionnaire to capture frequency of participation in 8-12-year-old children. In nine regions of seven European countries, parents of 813 children with cerebral palsy and 2939 children from the general populations completed the questionnaire. Frequency of participation for each question was dichotomised about the median; multivariable logistic regressions were carried out. In the general population, frequency of participation varied between countries. Children with cerebral palsy participated less frequently in many but not all areas of everyday life, compared with children from the general population. There was regional variation in the domains with reduced participation and in the magnitude of the differences. We discuss how this regional variation might be explained by the different environments in which children live. Attending a special school or class was not associated with further reduction in participation in most areas of everyday life.

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Year:  2008        PMID: 18571944     DOI: 10.1016/j.ejpn.2008.03.005

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  18 in total

1.  Study protocol: determinants of participation and quality of life of adolescents with cerebral palsy: a longitudinal study (SPARCLE2).

Authors:  Allan F Colver; Heather O Dickinson
Journal:  BMC Public Health       Date:  2010-05-26       Impact factor: 3.295

2.  How available to European children and young people with cerebral palsy are features of their environment that they need?

Authors:  Sandra Martina Espín-Tello; Allan Colver
Journal:  Res Dev Disabil       Date:  2017-10-05

3.  Testing ActiveYou II: Applying Cognitive Interviews in Improving Item Quality and Applicability of a Web-Based, Self-Report Instrument on Participation in Children with Disabilities.

Authors:  Friedolin Steinhardt; Reidun Jahnsen; Anne-Stine Dolva; Anna Ullenhag
Journal:  Int J Environ Res Public Health       Date:  2021-04-29       Impact factor: 3.390

4.  European study of frequency of participation of adolescents with and without cerebral palsy.

Authors:  Susan I Michelsen; Esben M Flachs; Mogens T Damsgaard; Jacqueline Parkes; Kathryn Parkinson; Marion Rapp; Catherine Arnaud; Malin Nystrand; Allan Colver; Jerome Fauconnier; Heather O Dickinson; Marco Marcelli; Peter Uldall
Journal:  Eur J Paediatr Neurol       Date:  2013-12-25       Impact factor: 3.140

5.  Dance program for physical rehabilitation and participation in children with cerebral palsy.

Authors:  Citlali López-Ortiz; Kim Gladden; Laura Deon; Jennifer Schmidt; Gay Girolami; Deborah Gaebler-Spira
Journal:  Arts Health       Date:  2011-06-13

6.  Predictors of participation of adolescents with cerebral palsy: A European multi-centre longitudinal study.

Authors:  Van Mô Dang; Allan Colver; Heather O Dickinson; Marco Marcelli; Susan I Michelsen; Jackie Parkes; Kathryn Parkinson; Marion Rapp; Catherine Arnaud; Malin Nystrand; Jérôme Fauconnier
Journal:  Res Dev Disabil       Date:  2014-11-14

7.  Self-reported quality of life of adolescents with cerebral palsy: a cross-sectional and longitudinal analysis.

Authors:  Allan Colver; Marion Rapp; Nora Eisemann; Virginie Ehlinger; Ute Thyen; Heather O Dickinson; Jackie Parkes; Kathryn Parkinson; Malin Nystrand; Jérôme Fauconnier; Marco Marcelli; Susan I Michelsen; Catherine Arnaud
Journal:  Lancet       Date:  2014-10-07       Impact factor: 79.321

8.  Systematic Review of Cerebral Palsy Registries/Surveillance Groups: Relationships between Registry Characteristics and Knowledge Dissemination.

Authors:  Donna S Hurley; Theresa Sukal-Moulton; Deborah Gaebler-Spira; Kristin J Krosschell; Larissa Pavone; Akmer Mutlu; Julius Pa Dewald; Michael E Msall
Journal:  Int J Phys Med Rehabil       Date:  2015-03-23

9.  Participation in life situations of 8-12 year old children with cerebral palsy: cross sectional European study.

Authors:  Jérôme Fauconnier; Heather O Dickinson; Eva Beckung; Marco Marcelli; Vicki McManus; Susan I Michelsen; Jackie Parkes; Kathryn N Parkinson; Ute Thyen; Catherine Arnaud; Allan Colver
Journal:  BMJ       Date:  2009-04-24

10.  Participation in everyday activities and quality of life in pre-teenage children living with cerebral palsy in South West Ireland.

Authors:  Vicki Mc Manus; Paul Corcoran; Ivan J Perry
Journal:  BMC Pediatr       Date:  2008-10-31       Impact factor: 2.125

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