The everyday experience of living with and managing a neurological condition (the LINC study): study design

Versnel, Joan and Packer, Tanya and Weeks, Lori E. and Brown, Jocelyn and Godwin, Marshall and Hutchinson, Susan and Kephart, George and MacKenzie, Diane and Roger, Kerstin and Stadnyk, Robin and Villeneuve, Michelle and Warner, Grace (2013) The everyday experience of living with and managing a neurological condition (the LINC study): study design. BMC Neurology, 13 (30). ISSN 1471-2377

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Abstract

Background: The impact of neurological conditions on individuals, families and society is increasing and having a significant economic impact in Canada. While some economic data is known, the human costs of living with a neurological condition are poorly understood and rarely factored into future burden analyses. The “Living with the Impact of a Neurological Condition (LINC)” study aims to fill this gap. It seeks to understand, for children and adults with neurological conditions, the supports and resources that make everyday life possible and meaningful. Methods/design: The LINC study is a nested study using mixed methods. We are interested in the following outcomes specifically: health status; resource utilization; self-management strategies; and participation. Three studies captured data from multiple sources, in multiple ways and from multiple perspectives. Study One: a populationbased survey of adults (n = 1500), aged 17 and over and parents (n = 200) of children aged 5 to 16 with a neurological condition. Study Two: a prospective cohort study of 140 adults and parents carried out using monthly telephone calls for 10 months; and Study Three: a multiple perspective case study (MPCS) of 12 adults and 6 parents of children with a neurological condition. For those individuals who participate in the MPCS, we will have data from all three studies giving us rich, in depth insights into their daily lives and how they cope with barriers to living in meaningful ways. Discussion: The LINC study will collect, for the first time in Canada, data that reflects the impact of living with a neurological condition from the perspectives of the individuals themselves. A variety of tools will be used in a combination, which is unique and innovative. This study will highlight the commonalities of burden that Canadians living with neurological conditions experience as well as their strategies for managing everyday life.

Item Type: Article
URI: http://research.library.mun.ca/id/eprint/1972
Item ID: 1972
Keywords: Participation framework, Self-management, Chronic disease, Services, Children, Youth adults, Parents, Disability
Department(s): Medicine, Faculty of
Date: 21 March 2013
Date Type: Publication
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