Research partnerships
VicHip brings together brilliant minds from around the world, fostering collaborative research and discovery for healthier hips.
We work with other hip studies and registries to improve the management of hip dysplasia globally and explore strategies to advance public health.
We look forward to sharing discoveries and developing innovative programs that could have a big impact on patients and families worldwide.
Generation Victoria
Generation Victoria (GenV) is a research project led by the Murdoch Children’s Research Institute. GenV is studying the health of Victorian children born between October 2021 and October 2023 and their parents. They aim to find faster and better ways to predict, prevent and treat various health issues.
If your child was born during this two-year period and has hip dysplasia, taking part in VicHip offers you the choice to be involved in GenV. As an opt-in option, this will allow the two studies to share information, including data already collected by other services. This could help VicHip find causes and treatments for hip dysplasia faster than we can today.
Participants in VicHip can choose to be contacted by GenV to learn more about their research and how to take part (this requires your consent). GenV will explain how it works and what data they share, so you have all the information you need before deciding to take part.
VicHip and GenV are excited to work together on research that could improve hip health around the world.
Global Hip Dysplasia Registry
The Global Hip Dysplasia Registry (GHDR) is a clinical registry with a large network of contributors from various countries. It is hosted by the British Columbia Children's Hospital Research Institute in Canada. They are working towards growing rich data and high-quality evidence in hip dysplasia literature. Like VicHip, the registry provides a platform to address the current gaps in knowledge of hip dysplasia and an opportunity to improve patient care worldwide.
VicHip shares data with GHDR, which brings together a wide range of information about hip dysplasia from other countries. The data can help researchers identify contributing factors or connections about hip dysplasia that would otherwise be difficult to find in one data set. If you join VicHip, you agree to share your de-identified data with the GHDR.
The partnership between VicHip and GHDR allows us to deepen our understanding of the natural history of hip dysplasia, study long-term outcomes and potentially change screening practices and monitoring protocols worldwide.
Have questions, feedback or want to get involved?
Please contact us
Proudly in partnership with
VicHip is funded by the Australian Government Department of Health and Aged Care under the Medical Research Future Fund grant 2015989.
Murdoch Children's Research Institute acknowledges the Traditional Custodians of lands on which we work and pay our respect to their Elders, past, present and emerging.