Co-Designing Anorexia Support and Treatment (Parents and Carers)
About this study
Research Team
Dr Michelle Yeo
Institution
Murdoch Children\'s Research Institute, Royal Children\'s Hospital
Funding Source
MRFF
Participants
People with lived experience of Family Based Treatment (FBT) for anorexia or atypical anorexia, including young people and parents/carers
What is Involved
If you take part, we will ask you to complete one online survey. At the end of the survey, you will be asked if you would be interested in participating in an individual interview and/or a focus group
Ethics Approval Number
117157
Contact Details
coast@mcri.edu.au
Visit website: redcap.mcri.edu.au
We are inviting you to take part in a project looking at lived experience of Family Based Treatment (FBT) for Anorexia Nervosa or Atypical Anorexia Nervosa, from the perspective of parents/ carers. In this project, we will examine the lived experience, both positive and negative, of Family Based Treatment for Anorexia Nervosa or Atypical Anorexia Nervosa (AN/AAN). We will be asking parents or carers with lived experience to take part. We would like to use what we learn to design a new adaptation of FBT, alongside people who experienced AN/AAN as children, parents/carers, and healthcare providers (clinicians). This project aims to explore lived experience of FBT for AN/AAN through surveys and individual interviews. We hope to better understand what works and what does not work in FBT for AN/AAN. We will then use focus groups to reflect on the themes from the survey and interviews and reflect on how to make changes to the FBT model of care.
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