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dc.rights.licenseopenen_US
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorKERVRAN, Charlotte
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorFRANCIS-OLIVIERO, Florence
dc.contributor.authorKRET, Marion
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBURTIN, Adrianna
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorRATEL, Rebecca
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorCLET, Estelle
dc.contributor.authorCOLLIN, Fidéline
dc.contributor.authorMARTIREN, Séverine
dc.contributor.authorBRANDET, Claire
dc.contributor.authorMARTIN-FERNANDEZ, Judith
dc.contributor.authorPERRIN, Sarah
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMONIN, Carla
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorCAMBON, Linda
hal.structure.identifierSommeil, Addiction et Neuropsychiatrie [Bordeaux] [SANPSY]
dc.contributor.authorAURIACOMBE, Marc
dc.contributor.authorSENTILHES, Loïc
dc.contributor.authorALLA, François
dc.date.accessioned2024-11-25T13:05:41Z
dc.date.available2024-11-25T13:05:41Z
dc.date.issued2024-11-12
dc.identifier.issn2044-6055en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203470
dc.description.abstractEnIn 2021, among French women who smoked when they knew they were pregnant, 59% still smoked at the end of pregnancy. Support for pregnant women to stop smoking must include a structured organisational perspective. The main objective of the study is to evaluate the effectiveness of the 5A-QUIT-N organisational intervention on smoking cessation at delivery among pregnant women who smoke during pregnancy. The overarching goal of the 5A-QUIT-N intervention, which aims to organise the healthcare professionals monitoring pregnancy, specialists in addiction and tobacco use, and clinical and training tools, using the 5As method. The 5A-QUIT-N intervention will be evaluated in a pragmatic stepped-wedge cluster randomised trial. Within each cluster, during the 6 months before (control) and after (intervention) the intervention, women who smoke tobacco during pregnancy will be enrolled during their maternity stay after delivery. A transition period is planned between the control and intervention periods to deploy the intervention. All participating women will be interviewed using a heteroquestionnaire to assess smoking cessation, tobacco use monitoring by healthcare professionals and individual factors associated with tobacco use during pregnancy. The primary outcome was the point prevalence of abstinence at delivery, which is the proportion of women reporting abstinence from smoking for at least 7 days at delivery. 4200 women who smoked tobacco during pregnancy will be recruited over the entire study period (33 months) to evaluate the effectiveness. An estimated 4585 participants will be included for all aims. The study will be implemented in accordance with French regulations. The study including the consent process has been independently reviewed and approved by the French ethical board 'CPP Ile de France I' on 10 February 2022 (No CPPIDF1-2022-DI08-cat.2). The results will be disseminated on various academic and non-academic platforms. The results will be reported in international peer-reviewed journals and presented at international and national conferences.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.enHumans
dc.subject.enFemale
dc.subject.enPregnancy
dc.subject.enSmoking Cessation
dc.subject.enFrance
dc.subject.enHealth Personnel
dc.subject.enPregnancy Complications
dc.subject.enRandomized Controlled Trials as Topic
dc.subject.enAdult
dc.subject.enTobacco Smoking
dc.title.enEffectiveness evaluation of an organisational intervention, targeting pregnancy and addiction care professionals, among women who have just given birth in maternity wards and smoked tobacco during pregnancy (5A-QUIT-N): study protocol for a stepped-wedge cluster randomised trial.
dc.title.alternativeBMJ Openen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1136/bmjopen-2024-087541en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed39532364en_US
bordeaux.journalBMJ Openen_US
bordeaux.pagee087541en_US
bordeaux.volume14en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue11en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.institutionCNRS
bordeaux.teamPHARES_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDInstitut National Du Canceren_US
bordeaux.identifier.funderIDInstitut pour la Recherche en Santé Publiqueen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04802282
hal.version1
hal.date.transferred2024-11-25T13:05:45Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=BMJ%20Open&rft.date=2024-11-12&rft.volume=14&rft.issue=11&rft.spage=e087541&rft.epage=e087541&rft.eissn=2044-6055&rft.issn=2044-6055&rft.au=KERVRAN,%20Charlotte&FRANCIS-OLIVIERO,%20Florence&KRET,%20Marion&BURTIN,%20Adrianna&RATEL,%20Rebecca&rft.genre=article


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