Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/100129
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dc.contributor.authorPerry, Y.en
dc.contributor.authorCalear, A.en
dc.contributor.authorMackinnon, A.en
dc.contributor.authorBatterham, P.en
dc.contributor.authorLicinio, J.en
dc.contributor.authorKing, C.en
dc.contributor.authorThomsen, N.en
dc.contributor.authorScott, J.en
dc.contributor.authorDonker, T.en
dc.contributor.authorMerry, S.en
dc.contributor.authorFleming, T.en
dc.contributor.authorStasiak, K.en
dc.contributor.authorWerner-Seidler, A.en
dc.contributor.authorChristensen, H.en
dc.date.issued2015en
dc.identifier.citationTrials, 2015; 16(1):1-17en
dc.identifier.issn1745-6215en
dc.identifier.issn1745-6215en
dc.identifier.urihttp://hdl.handle.net/2440/100129-
dc.description.abstractBackground: Evidence suggests that current treatments cannot fully alleviate the burden of disease associated with depression but that prevention approaches offer a promising opportunity to further reduce this burden. Adolescence is a critical period in the development of mental illness, and final school examinations are a significant and nearly universal stressor that may act as a trigger for mental health difficulties such as depression. The aim of the present trial is to investigate the impact of SPARX-R, an online, gamified intervention based on cognitive behavioural principles, on the prevention of depression in secondary school students before their final examinations. Methods/Design: Government, independent and Catholic secondary schools in New South Wales, Australia, will be recruited to participate in the trial. All students enrolled in their final year of high school (year 12) in participating schools will be invited to participate. To account for possible attrition, the target sample size was set at 1600 participants across 30 schools. Participating schools will be cluster randomised at the school level to receive either SPARX-R or lifeSTYLE, an attention-controlled placebo comparator. The control intervention is an online program aimed at maintaining a healthy lifestyle. The primary outcome will be symptoms of depression, and secondary outcomes will include symptoms of anxiety, suicidal ideation and behaviours, stigma and academic performance. Additional measures of cost-effectiveness, as well as process variables (e.g., adherence, acceptability) and potential predictors of response to treatment, will be collected. Consenting parents will be invited to complete measures regarding their own mental health and expectations for their child. Assessments will be conducted pre- and post-intervention and at 6- and 18-month follow-up. Primary analyses will compare changes in levels of depressive symptomatology for the intervention group relative to the attention control condition using mixed-effects model repeated-measures analyses to account for clustering within schools. Discussion: This is the first trial of a universal depression prevention intervention delivered to school students in advance of a specific, significant stressor. If found to be effective, this program may offer schools a new approach to preparing students for their final year of schooling. Trial registration: Australian New Zealand Clinical Trials Registry identifier: ACTRN12614000316606 . Registered 25 March 2014.en
dc.description.statementofresponsibilityYael Perry, Alison L. Calear, Andrew Mackinnon, Philip J. Batterham, Julio Licinio, Catherine King, Noel Thomsen, Jan Scott, Tara Donker, Sally Merry, Theresa Fleming, Karolina Stasiak, Aliza Werner-Seidler, and Helen Christensenen
dc.language.isoenen
dc.publisherBiomed Central Ltd.en
dc.rights© 2015 Perry et al. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en
dc.subjectAdolescents; CBT; computerised CBT; depression, e-health; prevention; RCT; schoolen
dc.titleTrial for the Prevention of Depression (TriPoD) in final-year secondary students: study protocol for a cluster randomised controlled trialen
dc.typeJournal articleen
dc.identifier.rmid0030048297en
dc.identifier.doi10.1186/s13063-015-0929-1en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1061072en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1013199en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1083311en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1056964en
dc.identifier.pubid216682-
pubs.library.collectionMedicine publicationsen
pubs.library.teamDS14en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidLicinio, J. [0000-0001-6905-5884]en
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