Research, Reports, and Insights on Home & Community Care.
Peer Reviewed Research
Directly funded home care in Canada, like other countries, is a key element of the public commitment to prioritize home care services that meet the needs of diverse older people and people with disabilities. Yet, as these programs expand in size and popularity, it is essential to reflect on the barriers that can be created through decisions in policy design.
With an aging population, an increase in home care client acuity, and post-COVID-19 concerns over long-term care, more attention is needed to improve the quality of home care. The demand for these services will continue to increase particularly for those living with dementia and their families. The findings of availability, acceptability, adaptability, and affordability as core to quality care can help lay the groundwork for a home care framework for persons living with dementia and their caregivers.
Many factors should be considered when we assess the suitability of both our built and social environments for aging in place, recognizing that these elements can have a direct effect on physical and social health and wellbeing. This article addresses benefits, challenges and strategies to aging in place.
As we recover from the COVID-19 pandemic and reflect on strategies to improve our public health response to future threats, it is imperative that we consider decent work for personal support workers who provide care for our most vulnerable. These findings highlight potential areas for labour policy reforms related to the PSW workforce.
The objective of this research is to identify, appraise and synthesize evidence on the effectiveness of complex interventions targeting reduction in social vulnerability for improving health related outcomes (mortality, function, cognition, subjective health and healthcare use) in older adults living in the community.
Across Ontario’s publicly funded home care system, the first wave of the COVID-19 pandemic significantly disrupted patterns of home care admissions, discharges, standardised assessments, as well as receipt of personal support, occupational therapy, and physical therapy services. The sector should prioritise both home care assessment and service delivery during a crisis to ensure persons who rely on these essential services are well-supported in the community.
This case study on Adult Day Programs (ADPs) at the Toronto Geriatric Centre employes a qualitative research strategy encompassing interviews and focus groups. Its purpose was to gather feedback from staff members, clients and family caregivers with the intention of identifying service gaps, crucial to developing the programs' effectiveness.
Caregiver burden is a common and significant problem with serious consequences not only for caregivers but also for the care provided to patients. These risks have also been exacerbated by the social isolation of the COVID‑19 pandemic. This research outlines how to apply a C.A.R.E framework to reduce caregiver stress.
The evidence included in this review supports the use of home‐based end‐of‐life care programmes for increasing the number of people who will die at home. Research that assesses the impact of home‐based end‐of‐life care on caregivers and admissions to hospital would be a useful addition to the evidence base, and might inform the delivery of these services.
The SCH is a grassroots, innovative integrated model of care that outlines a framework for upstream primary care assessments and interventions for older adults at risk of frailty. With creative mobilization of available resources and services any primary healthcare team can implement the SCH within their practice.
Home health organizations should employ a nuanced approach to improving quality, increasing compensation to permanent home health aides when the organization increases their use of contract home health aides and equally distributing benefits to home health aides when the organization does not rely as heavily on contract home health aides.
The aims of the study were to describe the characteristics of meals-on-wheels (MOW) recipients, including prevalence of malnutrition amongst those who have received input from the Nutrition and Wellbeing Service (NWS) and to explore whether the NWS had an impact on the nutritional status (malnutrition risk) of recipients over time.
Typically, older adults with MCC receive care from multiple healthcare providers across various care settings. For older adults with MCC living in the community, these healthcare providers are mainly from primary care and home care settings and include a broad range of providers such as nurses, physicians, social workers, pharmacists, physiotherapists, and personal support workers (or healthcare aides). Older adults with MCC and their family and friend caregivers (hereafter referred to as caregivers) experience their care to be focused on single conditions and lacking a holistic focus on the client and family.
The presentation will explore the common principle, concepts, core characteristics and components of integrated health and social services that support continuity of care. These concepts will be explored against the “Home-At-Last” (HAL) integrated initiative, a community-based program, situated in Ontario, Canada.
Attempts to rebalance health systems towards strengthened community-based care have been relatively unsuccessful. In order for rebalancing efforts to offer any form of staying power there first needs to be an understanding of the complexity of the community subsector to inform the types of inputs necessary to successfully expand community care avoiding further fragmentation and/or maintenance of the status quo.
Home or foster home care versus institutional long-term care for functionally dependent older people
This article attempts to establish whether dependent older people benefit from enhanced long-term home care services compared with placement in a long-term care institution. It also aimed to determine whether enhanced home care affects informal caregivers.
The objectives of this study are to identify what performance indicators make sense for home and community care and who has input in deciding these indicators? Findings suggest that state actors do recognize the calls from the home and community care NGOs to develop appropriate performance indicators for this sector, and to incorporate quality of life as an essential component of performance measurements.
Family Feedback on the Closure of Institutions for Persons with Intellectual Disabilities in Ontario
The study did identify factors that were related to individual differences within the sample. The variations from the majority were also consistent with the literature. Examples that contradict the overall story are provided through counter-stories.
Societal costs of home and hospital end-of-life care for palliative care patients in Ontario, Canada
Although patients in home-based palliative care had lower hospitalisation costs, they incurred much higher unpaid caregiver time costs and home care service costs than hospital-based patients. From a societal perspective, homebased palliative care may be just as expensive as hospital-based palliative care.
For an older adult with a hip fracture, the subsequent decline in function and mobility can be debilitating, resulting in a great burden placed on their caregivers and the health care system. Thus, this review will synthesize knowledge focusing on activities to maintain and restore function in older adult patients with CI once they have completed their active rehabilitation program and return home.
Governments and health care policy makers are trying to address the epidemic of chronic disease in Canada through primary care service reform, emphasis on patient-centred care, continuity of care and increased attention to the broader dimensions of health (29). Future changes in the health care system in Canada must account for provision of integrated care at both specialty institutions and community practices.
This study confirms low level of awareness of CSSs without acquiescence bias. Age, gender, income, community engagement and information about services all explain some of the variance in awareness of CSSs. Findings provide support for a social inequality model and provide practical implications for improved awareness and use of CSSs.
This article used the case of personal support work to highlight the extent to which analogous health care services are differentially compensated in the province of Ontario, based on the setting in which care is provided: to the extent that wage differences can be attributed to place alone, home-based workers are the victims of wage discrimination.
In response to a competitive request for proposals, the demonstration selected nonprofit agencies leading coalitions of stakeholders in five states—Iowa, North Carolina, Oregon, Pennsylvania, and Vermont—to participate in a 3-year demonstration of a variety of policy initiatives and management practice interventions.