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dc.contributor.authorJoa, Inge
dc.contributor.authorGisselgård, Jens
dc.contributor.authorBrønnick, Kolbjørn
dc.contributor.authorMcGlashan, Thomas
dc.contributor.authorJohannessen, Jan Olav
dc.date.accessioned2016-08-31T13:00:26Z
dc.date.available2016-08-31T13:00:26Z
dc.date.issued2015-04
dc.identifier.citationJoa, I. et al. (2015) Primary prevention of psychosis through interventions in the symptomatic prodromal phase, a pragmatic Norwegian Ultra High Risk study. BMC Psychiatrynb_NO
dc.identifier.urihttp://hdl.handle.net/11250/2403177
dc.descriptionThis is an Open Access article originally published in BMC Psychiatry, 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.nb_NO
dc.description.abstractBackground: Evidence has been accumulating that it may be possible to achieve prevention in psychotic disorders. The aim of the Prevention Of Psychosis (POP) study is to reduce the annual incidence of psychotic disorders in a catchment area population through detection and intervention in the prodromal phase of disorder. Prodromal patients will be recruited through information campaigns modelled on the Scandinavian early Treatment and Intervention in Psychosis (TIPS) study and assessed by low-threshold detection teams. Methods/Design: The study will use a parallel control design comparing the incidence of first episode psychotic disorders between two Norwegian catchment areas with prodromal detection and treatment (Stavanger and Fonna) with two catchment areas without a prodromal intervention program (Bergen and Østfold). The primary aim of the current study is to test the effect of a Prodromal Detection and Treatment program at the health care systems level. The study will investigate: 1) If the combination of information campaigns and detection teams modelled will help in identifying individuals (age 13–65, fulfilling study inclusion criteria) at high risk of developing psychosis early, and 2) If a graded, multi-modal treatment program will reduce rates of conversion compared to the rates seen in follow-along assessments. Discussion: Positive results could potentially revolutionize therapy by treating risk earlier rather than disorder later and could open a new era of early detection and intervention in psychosis. Negative results will suggest that the potential for psychosis is determined early in life and that research should focus more on genetically linked neurodevelopmental processes. If we can identify people about to become psychotic with high accuracy, we can track them to understand more about how psychosis unfolds. Appropriate intervention at this stage could also prevent or delay the onset of psychosis and/or subsequent deterioration, i.e., social and instrumental disability, suicide, aggressive behavior, affective- and cognitive deficits.nb_NO
dc.language.isoengnb_NO
dc.publisherBioMed Centralnb_NO
dc.rightsNavngivelse 3.0 Norge*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/no/*
dc.subjectpsykiatrinb_NO
dc.subjectpsykosenb_NO
dc.subjectschizophrenianb_NO
dc.subjectpsychosisnb_NO
dc.subjectprodromalnb_NO
dc.subjectultra-high risknb_NO
dc.subjectearly detectionnb_NO
dc.subjectschizofreninb_NO
dc.titlePrimary prevention of psychosis through interventions in the symptomatic prodromal phase, a pragmatic Norwegian Ultra High Risk studynb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.rights.holder© 2015 Joa et al.nb_NO
dc.subject.nsiVDP::Medical disciplines: 700::Clinical medical disciplines: 750::Psychiatry, child psychiatry: 757nb_NO
dc.source.pagenumber9nb_NO
dc.source.volume15nb_NO
dc.source.journalBMC Psychiatrynb_NO
dc.source.issue89nb_NO
dc.identifier.doi10.1186/s12888-015-0470-5


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