What is this Study about?

In Canada, 61% of people living with dementia (Plwd) live at home, with 87% of those living with an informal caregiver. Compared to caregivers of other older adults without dementia, caregivers of Plwd report higher levels of stress. However, interventions addressing caregiver stress directly have not been very effective. Newer research focuses on resilience, defined as a trajectory in which an individual can not only adapt but enhance and grow in challenging circumstances.

This research addresses several questions. We will investigate what resilience looks like for informal caregivers of Plwd, and what behaviours lead to and promote resiliency. We will also examine what the role of environmental (e.g., living arrangements) and individual (e.g., personality) factors are on caregiver resiliency . These studies will determine what factors influence a caregiver’s ability to participate in behaviours that promote resiliency.

I will form a caregiver research partner team who will participate in further developing research questions for a large-scale online survey study (200-250 people). Choice of survey measures will be guided by both existing research and research partners.

The results of this research will reveal what behaviours allow caregivers of Plwd to engage in resiliency .For example, maybe it may be the case that taking time for self-reflection allows for caregivers to be ‘resilient’, meaning they are able to grow and thrive, and don’t experience high levels of stress. Knowing these behaviours and strategies, as well as the role of environmental factors, will empower caregivers to
move towards resilience and decrease stress.

What is this Study about?

Help Us Improve Support for Alzheimer’s Caregivers

We are inviting caregivers, healthcare providers, community organizations, and Alzheimer’s societies to take part in a research study focused on improving support for people caring for individuals with Alzheimer’s disease.

What is this study about?
We know that caregiving is a journey that changes over time, but many caregivers don’t have access to tools or services that meet their evolving needs. This study aims to change that by bringing together caregivers and professionals to co-create practical resources and tools that support caregivers through each stage of the disease.

What will participation involve?
Participation will mostly take place virtually and includes online surveys, focus groups, and/or one-on-one interviews through secure platforms like Zoom or Microsoft Teams. You’ll be asked about your experiences with caregiving and the services available to you. Later, we’ll host in-person co-design sessions to work together on building useful tools and guidance for caregivers.

Why join?
By participating, you’ll have the chance to reflect on your experience, identify gaps in current services, and help shape resources that better support caregivers like you. You may also learn about services you didn’t know existed. Your input will directly inform more responsive and timely support for caregivers and people living with Alzheimer’s.

What is this Study about?

You are invited to participate in a research study that will help us understand the current end-of-life (i.e., last months, weeks, or days) nutrition practices in long-term care (LTC) homes. Your perspective based on your experiences working in LTC can help us to develop educational resources for team members who support residents receiving palliative care at the end of their life. We hope this education will foster positive changes in attitudes and practices.

What is this Study about?

This study aims to evaluate the acceptance and usability of the GuardIO Family Care app, a mobile application designed to support community safety for individuals living with dementia or mild cognitive impairment and their care partners. The study also aims to analyze mobility patterns collected from the app to explore how mobility data can contribute to the early detection of cognitive impairment. The findings will help improve app design, inform care strategies, and support early intervention efforts for individuals living with dementia or MCI.

What is this Study about?

Behavioral and emotional changes often accompany dementia and are a leading cause of long-term care placement, even more so than cognitive decline. This study is the first to explore how family caregivers make treatment decisions in response to these emotional and behavioural symptoms. We are interested in understanding whether caregivers turn to medications, consider non-pharmacological strategies such as environmental modifications, or use a combination of both. Using a quantitative behavioural economics model, this study will examine how caregivers weigh the risks and benefits of different treatment options. We are particularly interested in decision-making related to dopaminergic medications (formerly known as “antipsychotics”), which are commonly prescribed despite known risks for people with dementia. The information gathered will help guide the development of resources to better support family caregivers in navigating treatment decisions. Participation involves completing an anonymous online survey and is open to family caregivers involved in medical decision-making for a relative or close friend with dementia.

What is this Study about?

Participants will take part in a one-on-one interview (in person or online) to share thoughts on reminders and changes in behavior that should be tracked by the system. Interviews will last about 60 minutes. A short follow-up (20 minutes or less) may also be requested later to provide extra feedback on the system’s design.

What is this Study about?

The purpose of this study is to examine the effect of CARES-D for physiotherapists on learner knowledge, attitudes, and confidence in dementia. We will administer online questionnaires to practicing rehabilitation professionals in Canada who work with individuals with dementia to: 1) Assess changes in rehabilitation professionals' knowledge about dementia; 2) Evaluate shifts in attitudes toward individuals with dementia; 3) Measure improvements in confidence in managing dementia care; 4) Gather participant feedback on the CARES-D training program; 5) Compare pre- and post-training outcomes to determine the program's effectiveness.

What is this Study about?

The objective of this study is to understand: (1) what community-based interventions caregivers/care partners for persons living with young onset dementia (i.e., dementia diagnosed under the age of 65) are accessing across Southern Ontario; (2) caregivers/care partners perceptions towards the community-based interventions they have accessed; and (3) the reasons, if any, for not accessing community-based interventions.

The results of this study will be used to help inform the development and enhancement of community-based interventions for persons living with YOD and their caregivers/care partners, and is a part of my PhD dissertation.

What is this Study about?

This study looks at how an at-home nature-based virtual reality (VR) program may help people living with Alzheimer’s disease manage behavioural and psychological symptoms of dementia (BPSD), such as depression. Caregivers/study partners will have the option of taking part in the study and providing feedback regarding the VR intervention. This project will explore how VR can be used as a non-pharmacological approach to prolong aging in place for individuals with BPSD, as BPSD contributes to rates of institutionalization. This will take place completely remotely, in your own home.