Abstract
Objective. To describe the level of participation in leisure activities among children and youth with arthritis, as well as to identify the sociodemographic (age, sex, family income), disease-related (functional limitations, disease duration, pain, medication use, child’s need for assistance), and contextual factors (use of rehabilitation services, proximity of local recreation facilities, cost of activities) that may be associated.
Methods. Data from the Participation and Activity Limitation Survey (PALS) 2006, a Canadian postcensus survey, was analyzed. Bivariate and multivariable linear regression analyses were applied to examine the associations between the sample’s level of participation in leisure activities, and sociodemographic, disease-related, and contextual characteristics.
Results. In Canada in 2006, an estimated 4350 children ranging in age from 5 to 14 years were living with arthritis. Fifty-six percent of parents reported that arthritis restricted their child’s participation in leisure activities. Bivariate analysis showed that the availability of local recreational facilities, the affordability of activities, and the child not requiring any assistance were all associated (modified Bonferroni correction α < 0.005) with greater participation in various types of leisure activities. Multiple linear regressions showed that higher family income (β 0.47, 95% CI 0.09, 0.85) and greater perceived pain (β 0.59, 95% CI 0.07, 1.10) were positively associated with involvement in informal leisure.
Conclusion. Our findings underline the importance of considering contextual factors in developing treatment plans aimed at improving participation in leisure activities among children with arthritis. Future longitudinal studies targeting children living with arthritis could provide pertinent information on participation over fluctuations in disease status.
Footnotes
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Sabrina Cavallo was supported by a graduate training award from the MENTOR program (Canadian Institutes of Health Research), and the Fonds de la Recherche en Santé du Québec (FRSQ); Debbie Ehrmann Feldman was supported by a senior career award from FRSQ. Analyses for this manuscript were conducted at the Quebec Interuniversity Centre for Social Statistics (QICSS) of the Canadian Research Data Centre Network (CRDCN). Services provided by the QICSS are possible through financial or in-kind support from the Social Sciences and Humanities Research Council, the Canadian Institutes of Health Research, the Canadian Foundation for Innovation, Statistics Canada, the Fonds de Recherche du Québec – Santé, and Quebec universities. The views expressed in this article are those of the authors and do not necessarily reflect those of the CRDCN or its partners. Additional support from the Institut de Recherche en Santé Publique Université de Montréal.
- Accepted for publication March 3, 2015.






