This article is based on a co-design study. A co-design study is where researchers invite consumers and community partners to share their lived experiences and ideas to develop new initiatives or products. This study focused on making key features or ‘principles’ for a new cycling program called ‘CycLink’.
Cycling can help young people with disability stay active, spend time with family and friends, build skills, and gain independence. However, many young people and their families find it difficult to get started. This is because information, suitable equipment, and local cycling opportunities for people with disability can be hard to find.
In this study, researchers worked together with eight young people with disability, seven parents, and fourteen community partners, such as therapists, teachers, coaches, and cycling organisations. Using interviews, surveys, photographs, and workshops, the team explored what it is like for young people with disability to learn to cycle and what support they need to reach this goal. They looked for common themes among young people with disability, their parents, and community partners (i.e. ‘co-designers’). These themes helped the team design the principles for the CycLink program.
The co-designers described learning to cycle as a “roller coaster” with many ups and downs. Getting started was often the hardest part. Families needed to find relevant information, suitable equipment, and people who could help. Despite these challenges, cycling created ‘EPIC’ opportunities for young people with disability to:
![Infographic titled “Using Experience-Based Co-Design to Develop Principles of a Novel Cycling Intervention (CyClink)” published in Disability and Rehabilitation. A large heading reads, “Learning to cycle should feel EPIC!” At the centre is a bicycle wheel graphic surrounded by four principles: Connection, Exploration, Participation, and Independence. Around the wheel are photographs showing cycling activities, bike trials, adapted bicycles, family participation, and community riding experiences. Speech bubbles contain quotations from participants and stakeholders: Young person: “I am not alone... There's a lot of riders on that road. You can be with others.” Young person: “Just trying all the bikes. I definitely knew which bike didn't feel comfortable... when I sat on this bike I knew that I would do it.” Parent and young person dyad: “It was a little bit challenging until we cracked the code.. with a bike riding champion [occupational therapist]” Physiotherapist: “They didn't think it was possible to do a bike-riding activity as a family. And she managed like the 10 k's around Uluru. So they were just super proud of her.” Parent: “He really likes going up and down hills and going fast...he just gets very excited”. Teacher: “...the reality for some of our kids is they're not going to be able to drive a car. Being an independent rider is a really important skill for a lot of them” Young person: “it feels like a roller coaster, but I can control the speed and go as fast as I want.” Parent: “(Cycling) was not him playing and me watching. It was us doing something together.” The infographic highlights social connection, exploration, participation, and independence as key outcomes of cycling for young people with disability. Logos for the University of Melbourne, Australian Catholic University, and La Trobe University appear at the top. The bottom of the image contains the full research citation for Carey et al. (2026) describing the CyClink program.](https://healthy-trajectories.com.au/wp-content/uploads/2026/08/Carey-Toovey-Disability-and-Rehab-scaled.png)
The findings show that learning to cycle is about much more than riding a bike. Young people with disabilities, families, and community partners all play an important role. Providing better access to information, equipment, expertise, and supportive networks could help more young people with disability participate meaningfully in cycling and community life. The next steps are to further develop the program and to trial CycLink in the community with young people and families.
This project was funded by a seed grant from the University of Melbourne’s Melbourne Disability Institute and forms part of John Carey’s PhD thesis, funded through the Australian Government’s Research Training Program. The team acknowledges in-kind support from Prof Victoria Palmer and Dr Jennifer Bibb from the University of Melbourne’s co-design node of MISCH.
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