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dc.contributor.authorJohnsen, Anna T
dc.contributor.authorPetersen, Morten A
dc.contributor.authorGluud, Christian
dc.contributor.authorLindschou, Jane
dc.contributor.authorFayers, Peter
dc.contributor.authorSjøgren, Per
dc.contributor.authorPedersen, Lise
dc.contributor.authorNeergaard, Mette A
dc.contributor.authorVejlgaard, Tove Bahn
dc.contributor.authorDamkier, Anette
dc.contributor.authorNielsen, Jan B
dc.contributor.authorStrömgren, Annette S
dc.contributor.authorHigginson, Irene J
dc.contributor.authorGroenvold, Mogens
dc.date.accessioned2019-11-01T08:23:31Z
dc.date.available2019-11-01T08:23:31Z
dc.date.created2015-01-19T14:54:06Z
dc.date.issued2014
dc.identifier.citationTrials. 2014, 15 (376)nb_NO
dc.identifier.issn1745-6215
dc.identifier.urihttp://hdl.handle.net/11250/2626025
dc.description.abstractBackground Advanced cancer patients experience considerable symptoms, problems, and needs. Early referral of these patients to specialized palliative care (SPC) could offer improvements. The Danish Palliative Care Trial (DanPaCT) investigates whether patients with metastatic cancer will benefit from being referred to ‘early SPC’. DanPaCT is a multicenter, parallel-group, superiority clinical trial with 1:1 randomization. The planned sample size was 300 patients. The primary data collection for DanPaCT is finished. To prevent outcome reporting bias, selective reporting, and data-driven results, we present a detailed statistical analysis plan (SAP) for DanPaCT here. Results This SAP provides detailed descriptions of the statistical analyses of the primary and secondary outcomes in DanPaCT. The primary outcome is the change in the patient’s ‘primary need’. The ‘primary need’ is a patient-individualised outcome representing the score of the symptom or problem that had the highest intensity out of seven at baseline assessed with the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30). Secondary outcomes are the seven scales that are represented in the primary outcome, but each scale evaluated individually for all patients, and survival. The detailed description includes chosen significance levels, models for multiple imputations, sensitivity analyses and blinding. In addition, we discuss the patient-individualized primary outcome, blinding, missing data, multiplicity and the risk of bias. Conclusions Only few trials have investigated the effects of SPC. To our knowledge DanPaCT is the first trial to investigate screening based ‘early SPC’ for patients with metastatic cancer from a broad spectrum of cancer diagnosis.nb_NO
dc.language.isoengnb_NO
dc.publisherBioMed Centralnb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleDetailed statistical analysis plan for the Danish Palliative care trial (DanPaCT)nb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.volume15nb_NO
dc.source.journalTrialsnb_NO
dc.source.issue376nb_NO
dc.identifier.doi10.1186/1745-6215-15-376
dc.identifier.cristin1201264
dc.description.localcodeThis article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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.nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal