EYE-GEN: Enhancing Access for Youth with Eye Disease to GENomic Services
Researchers at Flinders University are investigating the barriers primary care providers face in accessing and delivering genomic services for individuals and families affected by childhood glaucoma, congenital cataracts, or retinoblastoma, to inform the co-design of primary care–level healthcare solutions.
Flinders University researchers are calling for general practitioners!
Why?
They are conducting focus groups (with the option for one-on-one interviews) to gather insights into the barriers you see and face when seeing families living with childhood eye disease (childhood glaucoma, congenital cataracts, retinoblastoma).
Your valuable input will help inform our workshops which aim to create tailored support for families and healthcare professionals seeing families with childhood eye disease.
Who can participate?
General practitioners and nurses currently working in Australia.
How do I sign up?
Join the conversation and contribute to the advancement of eye health education. Click the following link (https://qualtrics.flinders.edu.au/jfe/form/SV_5p42WPiApy4udkG) or scan the QR code in the image below to read the participant information sheet and to register your interest in participating in this research.
This study has been approved by the Flinders University Human Research Ethics Committee (ID 8843). Please contact Giorgina Maxwell (Genetic Counsellor) if you have any questions on (08) 8432 4265 or email giorgina.maxwell@flinders.edu.au.
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