Megan Prictor

Senior Lecturer

University of Melbourne

Australia

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Megan Prictor is a Senior Lecturer at the University of Melbourne, Australia. Her research areas focus on the impacts of digital health interventions, including direct-to-consumer genetic testing, electronic health records, and the recording of healthcare consultations. Recent articles highlight her work on patient perspectives in mental health care and the effectiveness of electronic quality improvement activities in chronic kidney disease management.

Articles (18)

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2025

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2023

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2022

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2022

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2022

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2021

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2021

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2021

Collaborators (8)

Michelle Kennedy (Wiradjuri)

AUSTRALIA

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Craig Nelson

Clinical Services Director Division of Western Health @ Home/Head of Unit Nephrology

Western Health

AUSTRALIA

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Adrian Laughlin

University of Melbourne

AUSTRALIA

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An Tran-Duy

Associate Professor

University of Melbourne

AUSTRALIA

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Shanton Chang

Professor

University of Melbourne

AUSTRALIA

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Jeanette Conrick

Lecturer

University of Melbourne

AUSTRALIA

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Harriet Teare

University of Oxford

UNITED KINGDOM

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Ralph Hampson

Associate Professor responsible for Online Programs, Working in Human Service Organisations, Engaging with Families, and Ageing, Health and Human Services..

University of Melbourne

AUSTRALIA

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Megan Prictor

Research Interests

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Articles (18)

Effectiveness of Electronic Quality Improvement Activities to Reduce Cardiovascular Disease Risk in People With Chronic Kidney Disease in General Practice: Cluster Randomized Trial With Active Control

The use and impacts of direct-to-consumer genetic testing for adults with an adoption or out-of-home care experience: A scoping review

Service Users’ Perspectives on an Integrated Electronic Care Record in Mental Health Care: Qualitative Vignette and Interview Study

Patient-Accessible Electronic Health Records and Information Practices in Mental Health Care Contexts: Scoping Review

Saving trouble, saving time: the role and impact of healthcare consultation recordings in Australian legal proceedings

How often are patients recording their healthcare consultations in Australia and why? An online survey

Can I record this? A scoping review of Australian hospital policies governing consultation recording

Evaluation of CTRL: a web application for dynamic consent and engagement with individuals involved in a cardiovascular genetic disorders cohort

Recording our genes: Stakeholder views on genetic test results in networked electronic medical records

WHERE DOES RESPONSIBILITY LIE? ANALYSING LEGAL AND REGULATORY RESPONSES TO FLAWED CLINICAL DECISION SUPPORT SYSTEMS WHEN PATIENTS SUFFER HARM

Ethics guidelines use and Indigenous governance and participation in Aboriginal and Torres Strait Islander health research: a national survey

Data Breach Notification Laws—Momentum Across the Asia-Pacific Region

‘As Long as It's Used for Beneficial Things’: An Investigation of non-Māori, Māori and Young People's Perceptions Regarding the Research use of the Aotearoa New Zealand Integrated Data Infrastructure (IDI)

Impact of Electronic Health Records on Information Practices in Mental Health Contexts: Scoping Review

Clinical Software and Bad Decisions: The “Practice Fusion” Settlement and Its Implications

Digital Mega-Studies as a New Research Paradigm: Governing the Health Research of the Future

Culturally Adaptive Governance—Building a New Framework for Equity in Aboriginal and Torres Strait Islander Health Research: Theoretical Basis, Ethics, Attributes and Evaluation

Reflections on dynamic consent in biomedical research: the story so far

Collaborators (8)

Michelle Kennedy (Wiradjuri)

Craig Nelson

Adrian Laughlin

An Tran-Duy

Shanton Chang

Jeanette Conrick

Harriet Teare

Ralph Hampson

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