Every year, our scientists and patient advisory group identify the studies and topics creating the most impact for people living with arthritis.
Uncover Our Focus for 2026Ongoing and completed studies across our full research portfolio, from prevention and treatment to care and health systems.
Explore Our ResearchMeet the scientists, clinicians, trainees, and patient advisory board members, driving discoveries
Meet Our TeamPeople living with arthritis guide our research priorities, shape study design, and ensure our work reflects real life.
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Scientific Study Title:
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Research Category
Life-changing arthritis research is only possible with your help!
Reason For Research
Arthritis in children and teens is considered a very rare disease. Children with arthritis suffer from fatigue, joint pain, stiffness and swelling causing reduced mobility. This results in joint damage and life-long disability. The financial cost to the family includes: medication costs; modified home and school environment; and lost family income due to absences or ability to work at all. The social impact to the child is missed school days, limited ability to play with other children and the image that they are different. It is very difficult for children and other adults to understand that arthritis is a disease for all ages, not just ‘for old people’. The impact to the child is failed or lower education, a future of low paying jobs or unemployment due to disability, and for many poor mental health. For the parent as the prime caregiver and tutor, this can result in anxiety, depression and loneliness. In-fact, the whole family unit is impacted. The goal is to reduce inequalities, reduce the cost and improve the lives of children living with arthritis. Children with arthritis and their families need a voice.
Execution of Research
The study will explore health-care system costs and impacts on families including financial, education, employment, productivity, well-being and quality of life. JIA PaCER patient research partners will co-design and conduct focus groups to shape the value framework and help identify potential interventions to reduce the burden of JIA. The patient partners on the team will be able to provide critical insights to what it is like to live with a chronic illness. They will bring their unique viewpoints based on their lived experience with JIA. The goal of the research project is to create a report reflecting their unique voices and patient experiences in transitioning from child to adult care for JIA.
Involvement
The ‘PAVE’ team is an international partnership of six countries (Canada, Germany, Belgium, Spain, Switzerland and Israel) including clinical leaders, researchers, social scientists and patient organizations. The researchers will work with with patient and family advocacy organizations including a partnership between the national Canadian patient organization Cassie and Friends, the European Network for Children with Arthritis (ENCA) and the Israeli Family Organizations.
We will also collaborate with six young adults living with juvenile idiopathic arthritis (JIA), who are recent graduates of the Patient and Community Engagement Research (PaCER) program through Continuing Education at the University of Calgary.