TrEAT Registry

Organisation / Service

University of Technology Sydney

The TrEAT Registry is a multi-centre, longitudinal CQR that collects clinician- and client-reported data across outpatient, day patient, residential, and inpatient settings. Data is collected at treatment commencement, during treatment, and at discharge or follow-up. Clients aged 13 years and older provide informed consent to contribute de-identified data to a research databank. Core measures include the Eating Disorder Examination Questionnaire (EDE-Q), Clinical Impairment Assessment (CIA), and Depression Anxiety and Stress Scale (DASS-21).

National Strategy Standards and Actions

Treatment

Action 4.1:  Treatment services to provide a model of care for eating disorders that is effective and evidence-based.  

Workforce

Action: 2.4: Health and mental health services to ensure that data and needs assessments underpin workforce planning and development for eating disorders and that outcome data is utilised and disseminated to drive ongoing continuous quality improvement and innovation.