Dados Bibliográficos

AUTOR(ES) S. Johnson , C. Kelly , M. MacDonald , Meaghan Sim , Katie Aubrecht , Barbara Hamilton-Hinch , PATRIK MARIER , Emily Reid-Musson , Mark G. Embrett , Lars K. Hallstrom , Shala Knocton , Logan Lawrence , Jasmine Mah , Elaine Moody
AFILIAÇÃO(ÕES) Research & Innovation, University of Windsor, Windsor, Canada, Department of Community Health Sciences, University of Manitoba, Winnipeg, MB, Canada, Dalhousie University, Department of Research and Innovation, Nova Scotia Health, Halifax, NS, Canada, Department of Sociology, St Francis Xavier University, Antigonish, NS, Canada, Department of Political Science, Concordia University, Montreal, QC, Canada, Prentice Institute and Political Science, University of Lethbridge, Lethbridge, AB, Canada
ANO 2023
TIPO Artigo
PERIÓDICO International Journal of Qualitative Methods
ISSN 1609-4069
E-ISSN 1609-4069
DOI 10.1177/16094069231197962
ADICIONADO EM 2025-08-18

Resumo

Nova Scotia's Supportive Care Program (SCP) is an individualized funding program that provides funds for people living with dementia (PLWD) or acquired brain injuries to purchase basic home care services such as personal care, respite, cleaning and cooking. The SCP has the potential to address the Quintuple Aim of enhancing care experience, improving population health, reducing costs, improving provider experience and improving health equity, yet qualitative evidence is lacking. The aim of this study is to use participatory program evaluation methods to evaluate the SCP and consider how effective it is in addressing the Quintuple Aim. The study objectives and corresponding methods are to (1) Co-develop a SCP logic model to guide the evaluation through consultations with a diverse group of stakeholders including PLWD, caregivers, care providers, researchers, government representatives, and nongovernment organizations, with attention to gender; (2) Evaluate the SCP based on the outcomes and outputs identified in the logic model using focus groups with PLWD, caregivers and home care providers, and interviews with PLWD and their caregivers; and (3) Mobilize knowledge about the ways the SCP addresses the Quintuple Aim through integrated knowledge translation activities with public, policy and research audiences. By focusing on clinically and socially vulnerable populations of PLWD and caregivers, the proposed evaluation of the SCP offers a valuable case in assessing the effectiveness of individually-funded home care in addressing the Quintuple Aim including health equity within the context of dementia care.

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