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Perspectives on Better Access: In-depth interviews with users and non-users of the initiative

dc.contributor.authorNewton, Danielleen
dc.contributor.authorWilliamson, Michelleen
dc.contributor.authorPirkis, Janeen
dc.contributor.authorBanfield, Michelleen
dc.contributor.authorBrophy, Lisaen
dc.contributor.authorMihalopoulos, Cathrineen
dc.contributor.authorHarris, Meredithen
dc.contributor.authorCurrier, Dianneen
dc.date.accessioned2026-07-29T20:41:07Z
dc.date.available2026-07-29T20:41:07Z
dc.date.issued2026en
dc.description.abstractObjective: The Better Access initiative enables clinical psychologists, psychologists, social workers and occupational therapists to offer sessions of psychological treatment to people with common mental disorders. Better Access services are listed on the Medicare Benefits Schedule which means that consumers only pay a percentage of the cost. This study sought the views of users and non-users of Better Access about the programme’s accessibility, appropriateness and outcomes. Methods: We conducted semi-structured interviews with participants recruited via two national lived experience networks: Beyond Blue’s BlueVoices and Lived Experience Australia. Results: We interviewed 23 people who had used Better Access in 2021 and 14 who had not. Participants suggested that, in general, Better Access operates smoothly, allows people to access high-quality care, and yields positive outcomes (e.g. improved functioning, reduced symptoms). However, they indicated that although Better Access makes care more affordable, out-of-pocket costs can still be prohibitive. They also queried whether the number of sessions available through the programme is sufficient. Conclusion: Better Access has many strengths, but it meets the needs of some better than others. Future reforms to Better Access should address accessibility and affordability.en
dc.description.sponsorshipThe authors disclosed receipt of the following financial support for the research, authorship and/or publication of this article: The evaluation of Better Access was funded by the Australian Government Department of Health, Disability and Ageing. This study was funded by the Australian Government Department of Health, Disability and Ageing, as part of the broader evaluation of Better Access. We would like to thank the two groups that were constituted to advise on the evaluation, the Clinical Advisory Group and the Stakeholder Engagement Group. We would like to acknowledge Beyond Blue and Lived Experience Australia for assisting us with recruiting participants for this study. We would also like to thank the participants themselves.en
dc.description.statusPeer-revieweden
dc.format.extent8en
dc.identifier.issn0004-8674en
dc.identifier.otherORCID:/0000-0002-3024-1687/work/221891211en
dc.identifier.scopus105031166655en
dc.identifier.urihttps://hdl.handle.net/1885/733813964
dc.language.isoenen
dc.rightsPublisher Copyright: © The Author(s) 2026. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).en
dc.sourceAustralian and New Zealand Journal of Psychiatryen
dc.subjectBetter Accessen
dc.subjectMedicareen
dc.subjectmental health servicesen
dc.subjectpeople with lived experienceen
dc.subjectPsychological therapyen
dc.titlePerspectives on Better Access: In-depth interviews with users and non-users of the initiativeen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage102en
local.bibliographicCitation.startpage95en
local.contributor.affiliationNewton, Danielle; University of Melbourneen
local.contributor.affiliationWilliamson, Michelle; University of Melbourneen
local.contributor.affiliationPirkis, Jane; University of Melbourneen
local.contributor.affiliationBanfield, Michelle; Centre for Mental Health Research, National Centre for Epidemiology and Population Health, ANU College of Law, Governance and Policy, The Australian National Universityen
local.contributor.affiliationBrophy, Lisa; University of Melbourneen
local.contributor.affiliationMihalopoulos, Cathrine; Monash Universityen
local.contributor.affiliationHarris, Meredith; University of Queenslanden
local.contributor.affiliationCurrier, Dianne; University of Melbourneen
local.identifier.citationvolume60en
local.identifier.doi10.1177/00048674251404766en
local.identifier.pure32adf4cb-7a08-42ad-b2d8-e206cb8bb176en
local.identifier.urlhttps://www.scopus.com/pages/publications/105031166655en
local.type.statusPublisheden

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