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Open Access research with a European policy impact...

The Strathprints institutional repository is a digital archive of University of Strathclyde's Open Access research outputs. Strathprints provides access to thousands of Open Access research papers by Strathclyde researchers, including by researchers from the European Policies Research Centre (EPRC).

EPRC is a leading institute in Europe for comparative research on public policy, with a particular focus on regional development policies. Spanning 30 European countries, EPRC research programmes have a strong emphasis on applied research and knowledge exchange, including the provision of policy advice to EU institutions and national and sub-national government authorities throughout Europe.

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Dietetic management of pediatric overweight : development and description of a practical and evidence-based behavioral approach

Stewart, L. and Houghton, Jan and Hughes, Adrienne and Pearson, Dympna and Reilly, John J (2005) Dietetic management of pediatric overweight : development and description of a practical and evidence-based behavioral approach. Journal of the American Dietetic Association, 105 (11). pp. 1810-1815. ISSN 0002-8223

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Abstract

There is great uncertainty over how to treat childhood overweight. Recent systematic reviews provide a consensus on the most promising elements of treatment, but no successful, generalizable, evidence-based treatment model is currently available. We describe a novel approach to treatment that is evidence-based, putting recommendations of recent systematic reviews into practice. The novel treatment uses a client-centered approach and behavioral change techniques to increase and maintain motivation for lifestyle change. It focuses on increasing physical activity, reducing sedentary behavior, and changing diet in children who are overweight (body mass index >98th percentile) and of elementary school age. Treatment lasts for 6 months and requires 5 to 6 hours of a dietetics professional’s time per patient (in contrast to more traditional, less intensive approaches in the United Kingdom, which invest approximately 1.5 hours per patient). Preliminary assessment of the program suggests that it is practical, and patient dropout is low. Formal evaluation of efficacy will not be available until completion of a randomized, controlled trial in 2006. This description of our novel treatment will enhance generalizability of the program if it is successful, and a detailed description will assist in development of other treatments even if it is unsuccessful.