Counting What Counts: Assessing Quality of Life and its Social Determinants Among Nursing Home Residents with Dementia

Author:

Hoben Matthias1,Dymchuk Emily2,Doupe Malcolm B3,Keefe Janice3,Aubrecht Katie4,Kelly Christine3,Stajduhar Kelli5,Banerjee Sube6,O'Rourke Hannah M2,Chamberlain Stephanie2,Beeber Anna7,Salma Jordana2,Jarrett Pamela8,Arya Amit9,Corbett Kyle2,Devkota Rashmi2,Ristau Melissa10,Shrestha Shovana2,Estabrooks Carole A2

Affiliation:

1. York University

2. University of Alberta

3. Max Rady College of Medicine, University of Manitoba

4. St. Francis Xavier University

5. University of Victoria

6. University of Nottingham

7. Johns Hopkins University

8. Dalhousie University

9. North York General Hospital

10. The Good Samaritan Society

Abstract

Abstract Background Maximizing quality of life (QoL) is a major goal of care for people with dementia in nursing homes (NHs). Social determinants are critical for residents' QoL. However, similar to the United States and other countries, most Canadian NHs routinely monitor and publicly report quality of care, but not resident QoL and its social determinants. Therefore, we lack robust, quantitative studies evaluating the association of multiple intersecting social determinants with NH residents’ QoL. The goal of this study is to address this critical knowledge gap. Methods We will recruit a random sample of 80 NHs from 5 Canadian provinces (Alberta, British Columbia, Manitoba, Nova Scotia, Ontario). We will stratify facilities by urban/rural location, for-profit/not-for-profit ownership, and size (above/below median number of beds among urban versus rural facilities in each province). In video-based structured interviews with care staff, we will complete QoL assessments for each of ~4,320 residents, using the DEMQOL-CH, a validated, feasible tool for this purpose. We will also assess resident’s social determinants of QoL, using items from validated Canadian population surveys. Health and quality of care data will come from routinely collected Resident Assessment Instrument – Minimum Data Set 2.0 records. Knowledge users (health system decision makers, Alzheimer Societies, NH managers, care staff, people with dementia and their family/friend caregivers) have been involved in the design of this study, and we will partner with them throughout the study. We will share and discuss study findings with knowledge users in web-based summits with embedded focus groups. This will provide much needed data on knowledge users' interpretations, usefulness and intended use of data on NH residents’ QoL and its health and social determinants. Discussion This large-scale, robust, quantitative study will address a major knowledge gap by assessing QoL and multiple intersecting social determinants of QoL among NH residents with dementia. We will also generate evidence on clusters of intersecting social determinants of QoL. This study will be a prerequisite for future studies to investigate in depth the mechanisms leading to QoL inequities in LTC, longitudinal studies to identify trajectories in QoL, and robust intervention studies aiming to reduce these inequities.

Publisher

Research Square Platform LLC

Reference113 articles.

1. Public Health Agency of Canada. A Dementia Strategy For Canada: Together we Aspire. Ottawa, ON: Public Health Agency of Canada; 2019.

2. Alzheimer’s Disease International. World Alzheimer Report 2018: The state of the art of dementia research: New frontiers. London: Alzheimer’s Disease International; 2018.

3. World Health Organization (WHO). Global action plan on the public health response to dementia 2017–2025. Geneva: WHO; 2017.

4. Alzheimer Europe. Dementia in Europe Yearbook 2018: Comparison of national dementia strategies in Europe. Luxembourg: Alzheimer Europe; 2018.

5. World Health Organization. Global status report on the public health response to dementia. Geneva: World Health Organization; 2021.

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