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EXPERTS II - How are patient and caregiver participation in health and social care shaped by experienced burden of treatment and social inequalities? Protocol for a qualitative synthesis.
May, Carl R; Chew-Graham, Carolyn A; Gallacher, Katie I; Gravenhorst, Katja C; Mair, Frances S; Nolte, Ellen; Richardson, Alison.
Affiliation
  • May CR; Department of Health Services Research and Policy, London School of Hygiene & Tropical Medicine, London, UK.
  • Chew-Graham CA; NIHR ARC North Thames, London, UK.
  • Gallacher KI; School of Medicine, Keele University, Keele, UK.
  • Gravenhorst KC; School of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Mair FS; Department of Health Services Research and Policy, London School of Hygiene & Tropical Medicine, London, UK.
  • Nolte E; NIHR ARC North Thames, London, UK.
  • Richardson A; School of Health and Wellbeing, University of Glasgow, Glasgow, UK.
NIHR Open Res ; 3: 31, 2023.
Article de En | MEDLINE | ID: mdl-37881470
Our experiences of illness are often complex. We may have to work hard too. We may need to monitor and record symptoms: take up different diets and physical activity; use different drugs and medical devices; develop expertise in using websites and information technology; coordinate input from health and care services; sometimes we have to work out how to pay for the services we need. How we get through this work is affected by our capacity to do it, and that is shaped by personal and wider resources, we can draw on. All of this is also affected by the services that are available to us, and by the ways our chances in life are shaped by income, ethnicity, education, gender, and age. The kinds of illnesses we have and how they progress, mean that these factors change over time. We call these changes trajectories. To better understand service user work and capacity, we will review published studies that tell us about people's everyday experiences of living with illnesses. We focus on three rarely studied trajectories. These are long-term conditions associated with significant disability; serious relapsing remitting disease; and rapidly progressing acute disease. We will first use existing research to build a framework in which we can describe and understand relevant aspects of the published studies. We will use this framework to extract relevant information from the studies. This will enable us to make a model of common features of service user work and capacity across different conditions, their trajectories, service organisation and delivery, and patterns of social and economic disadvantage. Finally, we will work with groups of service users and caregivers, and with health and social care professionals to apply the model to the development of strategies to reduce workload and improve service design for people with complex health problems.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: NIHR Open Res Année: 2023 Type de document: Article Pays d'affiliation: Royaume-Uni Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: NIHR Open Res Année: 2023 Type de document: Article Pays d'affiliation: Royaume-Uni Pays de publication: Royaume-Uni