PEP-Aus Consultation Phase: Participant Form
We want to hear from you!
The PEP-Aus project aims to develop and demonstrate that a cystic fibrosis (CF)-specific partnership-based communication program co-produced by healthcare professionals and people living with CF can be embedded within routine CF healthcare in Australia, and positively impact healthcare experiences.
We are seeking Australian CF community members and clinicians to be interviewed as part of the PEP-Aus Consultation phase. We are gathering clinician and community insights into their experiences with CF healthcare communication and partnership. This will help us identify what is working well, what is more challenging, areas of need and opportunities for improvement.
We want to speak with:
- People with CF, aged 13 and over
- Parents, family members, partners, carers and supporters of people with CF
- Healthcare professionals from multiple professional disciplines who care for people with CF, either within a CF clinic or in the community
- Representatives from CF-related non-government organisations (NGOs).
Click the link below or scan the QR code to access the form and submit your details if you would like to be part of the PEP-Aus consultation phase. One of the PEP-Aus research team will then contact you with more information.
Link to form: https://uwa.qualtrics.com/jfe/form/SV_4NmnxStWR6eLKkK
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