Do you know someone affected by a traumatic brain injury (TBI)? In Canada, about 1 in 50 people live with brain injuries, dramatically altering lives and making navigation through the healthcare system challenging. Further, many survivors lack the necessary support from family and peers, which makes the recovery journey difficult. The Wolvesâ Den, part of the Brain Changes Initiative, is a peer support and education group dedicated to improving the lives of TBI survivors. It promotes six pillars of brain health: exercise, cognitive training, mindfulness, nutrition, sleep, and reducing harmful exposures. Here, TBI survivors can share stories, meets experts, and learn how to enhance their recovery. This project aims to evaluate and expand the Wolvesâ Den program. We aim to conduct a comprehensive assessment to evaluate Wolvesâ Den. This includes qualitative and quantitative methods to collect feedback from members, refine the program, and improve offerings. The funding will also support expert sessions, facilitation, the creation of TBI-accessible session recaps, and outreach to attract more participants. Our goal is to ensure the program remains a leading resource for TBI recovery, continually adapting to meet community needs.
Research Location: University of Victoria
Population aging: Co-development of a research agenda on supports to stay at home from the perspective of older adults and caregivers with lived experiences in rural and remote communities
In rural and remote communities across North Vancouver Island, there is a growing number of older adults who need supports to stay at home. This region has a disproportionately higher proportion of older adults in the province. With changing demographics due to out-migration of young workers (for urban job opportunities) and in-migration of older adults (due to lower cost of living and desirable retirement area), keeping up with services has been more challenging than in other places.
This project seeks to build community-engaged patient-oriented research partnerships with social-sector agencies, service providers, private businesses, government partners, and people from local communities in rural and remote locations within North Vancouver Island. Together, we will gather uncertainties facing vulnerable older adults in rural and remote communities about staying at home, and jointly plan a co-design workshop to develop a plan to engage researchers, research users, and funders with our findings.
Project outcomes include 1) research agenda on aging at home in rural and remote communities; and 2) network of partners and collaborators for future research and grant applications.
Developing a scale-up and evaluation plan for the Healthy Hips and Knees exercise program across B.C.
Hip and knee replacements are common procedures in Canada that improve mobility and reduce pain for individuals suffering from severe arthritis. To support pre- and post-surgical care, tailored exercise programs are integral. Unfortunately, access is often limited. This is especially true in rural areas, where cultural and language barriers persist. The Healthy Hips and Knees program offered by YMCA BC caters to those awaiting or recovering from surgery. Despite high demand, the program is currently available only in Prince George. To address this, YMCA BC hopes to expand its reach across British Columbia. The research team will collaborate with YMCA-BC to co-develop a research agenda. We will develop a plan to increase program reach and accessibility, particularly in underserved communities and groups. We will also ensure the program can continue over time. In addition, we have an evaluation plan to check how effective the program is, how well it is being adopted and implemented, and how it is maintained. This project will enhance care delivery for people with hip and knee replacements while identifying funding opportunities to sustain program expansion.
Healthy youth then, healthy adults now? Strategic planning for the midlife follow-up of the Victoria Healthy Youth Survey
Adolescence (ages 12-18) and young adulthood (ages 19-29) are typically the time when individuals establish autonomy and independence, develop healthy habits (e.g., exercise and nutritional food preferences), form and maintain healthy relationships, and build capacity for economic success. Poor physical health and health habits in these life periods contribute to later risks for disease and associated costs. Yet, we do not have Canadian data that connect health across adolescence and young adulthood to long-term health in early mid-life (ages 35-45). The proposed project builds on an existing and robust community-based sample, the Victoria Health Youth Survey (V-HYS) which began in 2003 (N=662; ages 12-18). Our team will partner with Drs. Fyfe and Kay (Island Health) and Dr. Thumath (Ministry of Health) to develop a plan to collect follow-up data from these now adults including evidence-based measures of physical health, mental health, substance use, healthy relationships, and social determinants of health. Our partnerships will ensure findings provide information about what matters for health long-term for Canadians and inform policy responses that can support midlife health, mental health, education, labour, and social supports.
Community Collaboration in the Gamification of a Proactive mHealth Intervention for Late-Life Cognitive Health
Subjective cognitive decline (SCD) is a likely precursor to dementia. With no known cure for dementia, and a rapidly aging world population, there is great need for research that targets reducing risk. Our team has developed and pilot-tested an mHealth-app-based psychoeducation intervention targeting cognitive health promotion for older adults; the results of this pilot study reflected a highly feasible intervention, but that many participants wanted an âextra challengeâ in learning and applying their new knowledge. The proposed project will work with knowledge users (e.g., people with SCD or lived experience of dementia and related disorders, family members, caregivers, clinicians, and advocates) to develop a plan for enhancing engagement through gamification. We will achieve this goal by consulting with knowledge users through a working group of persons with lived experience (PWLE), researchers, developers, and a clinician. This working group will identify the priorities of knowledge users for the enhancement of the intervention and how to move forward. This project will also disseminate knowledge gained from the working group consultations to research users via a public forum, an academic paper, and a series of infographics.
Cannabis Substitution of Alcohol as a Component of Managed Alcohol Programs: Co-Developing and Disseminating Research Evidence from a Recent Pilot Project.
We propose to come together with MAP site partners and people with lived and living experience of substance use to discuss findings from a recent pilot evaluation of cannabis substitution in MAPs, with the aim of contributing evidence to the well-established knowledge base for MAP. During this gathering, attendees will co-develop a KT strategy to package evidence for different audiences and plan to disseminate this evidence. Developing a KT strategy, including opportunities for knowledge mobilization, will support partners to review robust data related to cannabis as a harm reduction alternative to alcohol and other drugs, improve and sustain their current programs, and create evidence-based recommendations for other harm reduction organizations that want to implement cannabis substitution.
Our ultimate goal is to contribute to the development, implementation, and improvement of cannabis programs in harm reduction organizations, providing a safer alternative to alcohol and positively influencing the health of people with alcohol disorders. Dissemination of evidence will also grow the body of knowledge around cannabis substitution for other drugs, including opioids, to influence advocacy efforts and policy change.
Enhancing Knowledge Translation in Pain Management Through an Integrative Video Blog Series
This project aims to expand a well-established online video blog that brings together pain researchers, clinicians and patient partners to share critical insights about pain challenges and management. Season 5 will reintegrate our initial approach by mixing responses from all stakeholders. The project plans to align with an event co-hosted with Pain BC or the Canadian Pain Society to maximize impact and outreach.
Sharing Our Tools: A Workshop Series to Share Practical Tools for Unlearning & Undoing White Supremacy and Indigenous-Specific Racism for Population & Public Health
From 2021-2023, the BC Office of the Provincial Health Officer engaged in a CIHR and HRBC funded research project called, âUnlearning & Undoing White Supremacy in the OPHOâ (The U&U Project). We built and used tools to unlearn, monitor, and undo white supremacy in our structures, policies, practices, norms, and values.
This is an important way we are working towards upholding instructions we have received, including in the Truth & Reconciliation Calls to Action, Missing & Murdered Indigenous Women, Girls & 2SLGBTQQIA+ Calls for Justice, and In Plain Sight Recommendations.
Elders and Indigenous health leaders have told us that our tools are valuable and trustworthy. Settler health leaders and practitioners have shared that our tools offer tangible and meaningful ways to pick up the work of eradicating Indigenous specific racism.
Now, we plan to build a series of hosted and self-directed workshops to share our U&U tools more broadly.
Aim 1 – Build workshop curriculum for our U&U Tools
Aim 2 – Deliver workshops throughout BCâs population & public health ecosystem
Aim 3 – Build a website & YouTube channel to share materials
Aim 4 â Submit tools & findings for publication in peer reviewed journals
Extending the Reach of the Flipping Stigma on its Ear Toolkit: Translating and Transforming the Toolkit for the Chinese Community
The purpose of this knowledge translation project is to extend the reach of the Flipping Stigma on its Ear Toolkit, a research output that is a web-based education and advocacy tool developed by an Action Group of people with lived experience of dementia. Currently this toolkit (flippingstigma.com), which is focused on addressing dementia-related stigma and discrimination, is only available in English. This project will focus on translating and transforming the toolkit for the Chinese community. We will do this by working closely with a Knowledge Translation Team (KTT) of people with lived experience of dementia, care partners, health care professionals, and other members of the Chinese community. We will first arrange for a translation of the toolkit into Traditional Chinese characters. A beta version of the Chinese toolkit will be created online. Then our team will meet with the KTT over a series of online meetings to review the beta version. The goal of these KTT meetings will be to explore the beta version (translated) of the toolkit and help to transform it into a culturally relevant and sensitive tool for the Chinese community. As a final outcome of this project, a Chinese version of the toolkit will be officially released.
Novel STI Care and Prevention for Group Sex Communities
Group sex is an important health phenomenon, with an estimated one-in-ten people engaging in group sex at some point in their life. Group sex can be a source of pleasure and belonging but may increase risk of sexually transmitted infections (STIs). Despite its estimated prevalence, there has been little research on STI prevention and care among people who have group sex. Most group sex research has been done outside Canada and has focused only on men who have sex with men, excluding other sexualities and genders. My goal is to improve the STI outcomes for people who have group sex in Canada and beyond. My research focuses on 1) community-based knowledge around what makes group sex uniquely risky when it comes to STIs, 2) what STI prevention strategies people use during group sex and how effective they are, and 3) the barriers that healthcare providers face in providing STI care to people having group sex. Based on my findings, I will work closely with group sex community members to develop educational materials and support resources to improve STI prevention and care. Ultimately, I hope to reduce STIs and their negative impact on the health of this diverse stigmatized population.