White papers and research reports

White papers are research-based report addressing an issue or topic. Unlike journal articles they are not externally peer reviewed nor are they constrained by the format requirement of a journal publisher. The purpose of a white paper is to give the reader an understanding of the topic and the related research. Research reports are often the report of the work and findings of a funded project. These reports and white papers share earlier research from RePADD research that may not other be easily retrieved.

What do older First Nations people from Adelaide, South Australia and Hamilton, Aotearoa New Zealand need to receive culturally safe palliative care using telehealth? Frey R, Collier A, Allsop M, Shearing T, Paardekooper C, Reddy R.

Evaluating the Impact of Online Health Information: A Scoping Review of Measures. Damarell RA, Christian C, Juhrmann M, Tieman J.

Drawing on Gerontological Approaches to Inform Allied Health Best Practices in Palliative Aged Care. Yeo Z, Tieman J, George S, Farrer O.

Australian General Practitioner Perspectives on their Support for Bereaved Patients: A Cross-Sectional Survey. Tieman J, Swetenham K, Holden D.

Bridging Gaps in Palliative Care Access: A Narrative Review of Navigation Models. Swetenham K, Holden D, Ricci M, Bisset A.

Unpaid Carers' Forum: Recognition, Support, Action. Tieman J, Javanparast S.

Qualitative Interviews with Registered Nurses who Work Concurrently as a Death Doula. Rawlings D, Winsall M, Miller-Lewis L, Swetenham K, Tieman J.

Death Doulas in the News: A Media Scoping Study. Pimenta JL, Pedroso A, Tieman J, Rawlings D.

CareSearch Quality Processes: Ensuring reliability and applicability across diverse stakeholder groups. Erny-Albrecht K, Tieman J.

National Death Doula Roundtable. Rawlings D, Mills S, Miller-Lewis L, Swetenham K, Tieman J.

Supporting the Grief, Loss and Bereavement Needs of Families of Older People Living in Residential Aged Care. Tieman J, Vandersman P, Brooksbank M, Swetenham K.

Relationships of eHealth Literacy to Socio-Demographic Characteristics and Engagement in Online Learning: A Quantitative Study. Tieman, J, De Valle, M, Miller-Lewis, L.

Dying, a normal part of life: what learners see as the one thing they could change in the workplace to more appropriately provide end-of-life care. Rawlings D, Devery K, Tieman J, and Winsall M.

End-of-Life Online Health Education Uptake and Usage by Australian Health Professionals: Urban, Rural and Remote Settings. Devery K, Yin H, Morgan D, Rawlings D.

Identifying the Priority Evidence-Practice Gaps in Palliative Care: Health Professional Perspectives. Trenerry C, Damarell R, Tieman J.

‘My Learning’: Results of Pre-Test, Post-Test Evaluation, Tieman J, Rawlings D, Moores C.

Determining the Effect of Advance Care Planning in Palliative and End-of-Life Care, Tieman J, Bradley S.

Finding what works: a resource for discovering interdisplinary evidence about stroke, Hayman S, Tieman J, Kortman B, Lennon S, Laver K, Crotty M

Report on the Development of Two Search Filters for Retrieving the Sarcoma Literature. Lawrence M, Tieman J.

Report on the Development of a Glaucoma Search Filter. Tieman, J, Craig, J, Shaheem, Y.

Managing the Knowledge Base for Primary Health Care, Damarell R, Tieman J, Lawrence M.

Metrics, Measures and Meanings: Evaluating the CareSearch Website. Tieman J, Martin P.

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