Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/35465
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dc.contributor.authorNotley, Caitlinen_UK
dc.contributor.authorBrown, Tracey Jen_UK
dc.contributor.authorBauld, Lindaen_UK
dc.contributor.authorClark, Allan Ben_UK
dc.contributor.authorDuneclift, Sharonen_UK
dc.contributor.authorGilroy, Vickyen_UK
dc.contributor.authorHarris, Tessen_UK
dc.contributor.authorHardeman, Wendyen_UK
dc.contributor.authorHolland, Richarden_UK
dc.contributor.authorHoward, Gregoryen_UK
dc.contributor.authorMan, Mei-Seeen_UK
dc.contributor.authorNaughton, Felixen_UK
dc.contributor.authorSmith, Danen_UK
dc.contributor.authorTurner, Daviden_UK
dc.contributor.authorUssher, Michaelen_UK
dc.date.accessioned2023-10-18T00:00:38Z-
dc.date.available2023-10-18T00:00:38Z-
dc.date.issued2023-09-04en_UK
dc.identifier.othere076458en_UK
dc.identifier.urihttp://hdl.handle.net/1893/35465-
dc.description.abstractIntroduction Many people quit smoking during pregnancy, but postpartum smoking relapse is common. Maintaining smoking abstinence achieved during pregnancy is key to improving maternal and child health. There are no evidence-based interventions for preventing postpartum smoking relapse. This trial aims to determine whether an intervention to prevent postpartum relapse is effective and cost-effective. Methods and analysis A randomised controlled trial of a complex intervention to prevent postpartum smoking relapse (BabyBreathe), with internal pilot, economic and process evaluations. Participants are adults who are pregnant and who report having quit smoking in the 12 months before, or during pregnancy. Participants are eligible if they read and understand English, and provide informed consent. Following consent and biochemical validation of smoking abstinence, participants are randomised to intervention or usual care/control (no specific relapse prevention support). The BabyBreathe intervention consists of manualised advice from a trained member of the health visiting service, health information leaflets for participants and partners, access to the BabyBreathe website and app. At the time of birth, participants are posted the BabyBreathe box and support is provided by text message for up to 12 months postpartum. Target sample size is 880, recruiting across midwifery services at four hubs in England and Scotland and through remote advertising in England, Scotland, Wales and Northern Ireland. Outcomes are collected at 6 and 12 months. The primary outcome is self-reported sustained smoking abstinence at 12 months, carbon monoxide verified. Secondary outcomes include self-reported abstinence, time to relapse, partner smoking status and quality of life. Ethics and dissemination The trial was approved by the North West Preston Research Ethics committee (21/NW/0017). Dissemination will include publication in peer-reviewed journals, presentation at academic and public conferences including patient and public involvement and to policymakers and practitioners.en_UK
dc.language.isoenen_UK
dc.publisherBMJen_UK
dc.relationNotley C, Brown TJ, Bauld L, Clark AB, Duneclift S, Gilroy V, Harris T, Hardeman W, Holland R, Howard G, Man M, Naughton F, Smith D, Turner D & Ussher M (2023) BabyBreathe trial: protocol for a randomised controlled trial of a complex intervention to prevent postpartum return to smoking. <i>BMJ Open</i>, 13 (9), Art. No.: e076458. https://doi.org/10.1136/bmjopen-2023-076458en_UK
dc.rights© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectGeneral Medicineen_UK
dc.titleBabyBreathe trial: protocol for a randomised controlled trial of a complex intervention to prevent postpartum return to smokingen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1136/bmjopen-2023-076458en_UK
dc.identifier.pmid37666562en_UK
dc.citation.jtitleBMJ Openen_UK
dc.citation.issn2044-6055en_UK
dc.citation.volume13en_UK
dc.citation.issue9en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderNIHR National Institute for Health Researchen_UK
dc.author.emailaileen.paton@stir.ac.uken_UK
dc.citation.date04/09/2023en_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationIndependenten_UK
dc.contributor.affiliationInstitute of Health Visitingen_UK
dc.contributor.affiliationSt George's, University of Londonen_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationUniversity of Exeteren_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationUniversity of East Angliaen_UK
dc.contributor.affiliationSt George's, University of Londonen_UK
dc.identifier.scopusid2-s2.0-85169848749en_UK
dc.identifier.wtid1939213en_UK
dc.contributor.orcid0000-0003-0876-3304en_UK
dc.contributor.orcid0000-0003-4381-5974en_UK
dc.contributor.orcid0000-0002-8671-1553en_UK
dc.contributor.orcid0000-0001-9790-2796en_UK
dc.contributor.orcid0000-0002-0995-7955en_UK
dc.date.accepted2023-08-04en_UK
dcterms.dateAccepted2023-08-04en_UK
dc.date.filedepositdate2023-10-17en_UK
dc.relation.funderprojectBabybreathe Trial (A randomised controlled trial of a complex intervention to prevent return to smoking postpartum)en_UK
dc.relation.funderrefNIHR129074en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorNotley, Caitlin|0000-0003-0876-3304en_UK
local.rioxx.authorBrown, Tracey J|0000-0003-4381-5974en_UK
local.rioxx.authorBauld, Linda|en_UK
local.rioxx.authorClark, Allan B|en_UK
local.rioxx.authorDuneclift, Sharon|en_UK
local.rioxx.authorGilroy, Vicky|en_UK
local.rioxx.authorHarris, Tess|0000-0002-8671-1553en_UK
local.rioxx.authorHardeman, Wendy|en_UK
local.rioxx.authorHolland, Richard|en_UK
local.rioxx.authorHoward, Gregory|en_UK
local.rioxx.authorMan, Mei-See|en_UK
local.rioxx.authorNaughton, Felix|0000-0001-9790-2796en_UK
local.rioxx.authorSmith, Dan|en_UK
local.rioxx.authorTurner, David|en_UK
local.rioxx.authorUssher, Michael|0000-0002-0995-7955en_UK
local.rioxx.projectNIHR129074|National Institute for Health Research|http://dx.doi.org/10.13039/501100000272en_UK
local.rioxx.freetoreaddate2023-10-17en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2023-10-17|en_UK
local.rioxx.filenamee076458.full.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source2044-6055en_UK
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