Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/30500
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dc.contributor.authorBick, Debraen_UK
dc.contributor.authorTaylor, Cathen_UK
dc.contributor.authorBhavnani, Vanitaen_UK
dc.contributor.authorHealey, Andyen_UK
dc.contributor.authorSeed, Paulen_UK
dc.contributor.authorRoberts, Sarahen_UK
dc.contributor.authorZasada, Magdelenaen_UK
dc.contributor.authorAvery, Amandaen_UK
dc.contributor.authorCraig, Victoriaen_UK
dc.contributor.authorKhazaezadah, Ninaen_UK
dc.contributor.authorMcMullen, Sarahen_UK
dc.contributor.authorO’Connor, Sheilaen_UK
dc.contributor.authorOki, Bimpien_UK
dc.contributor.authorOteng Ntim, Eugeneen_UK
dc.contributor.authorPoston, Lucillaen_UK
dc.contributor.authorUssher, Michaelen_UK
dc.date.accessioned2019-12-06T01:02:10Z-
dc.date.available2019-12-06T01:02:10Z-
dc.date.issued2020-04en_UK
dc.identifier.urihttp://hdl.handle.net/1893/30500-
dc.description.abstractObjectives: To assess feasibility of a future randomised controlled trial (RCT) of clinical and cost-effectiveness of lifestyle information and commercial weight-management groups to support postnatal weight management to 12 months post-birth. Design: Two-arm feasibility trial, with nested mixed-methods process evaluation. Setting: Inner-city unit, South England. Population: Women with BMIs ≥25kg/m2 at pregnancy booking or normal BMIs (18.5kg/m2-24.9kg/m2) identified with excessive gestational weight gain at 36 weeks gestation. Methods: Randomised to standard care plus commercial weight-management sessions commencing 8-16 weeks postnatally or standard care only. Main outcomes: Feasibility outcomes included assessment of recruitment, retention, acceptability, and economic data collation. Primary and secondary endpoints included difference between groups in weight 12 months postnatally compared with booking (proposed primary outcome for a future trial), diet, physical activity, smoking, alcohol, mental health, infant feeding, NHS resource use. Results: 193 women were randomised; 98 intervention and 95 control; only four women had excessive gestational weight gain. A slightly greater weight change was found among intervention women at 12 months, with greatest benefit. among women attending 10+ weight management sessions. There was >80% follow-up to 12 months, low risk of contamination and no group differences in trial completion. Conclusion: It was feasible to recruit and retain women with BMIs≥25kg/m2 to an intervention to support postnatal weight management; identification of excessive gestational weight gain requires consideration. Economic modelling could inform out-of-trial costs and benefits in a future trial. A definitive trial is an important next step.en_UK
dc.language.isoenen_UK
dc.publisherWileyen_UK
dc.relationBick D, Taylor C, Bhavnani V, Healey A, Seed P, Roberts S, Zasada M, Avery A, Craig V, Khazaezadah N, McMullen S, O’Connor S, Oki B, Oteng Ntim E, Poston L & Ussher M (2020) Lifestyle information and commercial weight management groups to support maternal postnatal weight management and positive lifestyle behaviour: the SWAN feasibility randomised controlled trial. BJOG: An International Journal of Obstetrics and Gynecology, 127 (5), pp. 636-645. https://doi.org/10.1111/1471-0528.16043en_UK
dc.rights© 2019 The Authors. BJOG: An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd on behalf of Royal College of Obstetricians and Gynaecologists This is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectPostnatalen_UK
dc.subjectweight managementen_UK
dc.subjectrandomised controlled trialen_UK
dc.subjectfeasibilityen_UK
dc.titleLifestyle information and commercial weight management groups to support maternal postnatal weight management and positive lifestyle behaviour: the SWAN feasibility randomised controlled trialen_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate2020-12-06en_UK
dc.identifier.doi10.1111/1471-0528.16043en_UK
dc.identifier.pmid31808248en_UK
dc.citation.jtitleBJOG: An International Journal of Obstetrics and Gynaecologyen_UK
dc.citation.issn1471-0528en_UK
dc.citation.issn1470-0328en_UK
dc.citation.volume127en_UK
dc.citation.issue5en_UK
dc.citation.spage636en_UK
dc.citation.epage645en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderNational Institute for Health Researchen_UK
dc.author.emailmichael.ussher@stir.ac.uken_UK
dc.citation.date05/12/2019en_UK
dc.contributor.affiliationUniversity of Warwicken_UK
dc.contributor.affiliationUniversity of Surreyen_UK
dc.contributor.affiliationNational Childbirth Trusten_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.contributor.affiliationUniversity of Surreyen_UK
dc.contributor.affiliationUniversity of Nottinghamen_UK
dc.contributor.affiliationGuy's and St Thomas' NHS Foundation Trusten_UK
dc.contributor.affiliationGuy's and St Thomas' NHS Foundation Trusten_UK
dc.contributor.affiliationNational Childbirth Trusten_UK
dc.contributor.affiliationGuy's and St Thomas' NHS Foundation Trusten_UK
dc.contributor.affiliationLambeth Councilen_UK
dc.contributor.affiliationGuy's and St Thomas' NHS Foundation Trusten_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.contributor.affiliationInstitute for Social Marketingen_UK
dc.identifier.isiWOS:000504686200001en_UK
dc.identifier.scopusid2-s2.0-85078586091en_UK
dc.identifier.wtid1490271en_UK
dc.contributor.orcid0000-0002-0995-7955en_UK
dc.date.accepted2019-11-25en_UK
dcterms.dateAccepted2019-11-25en_UK
dc.date.filedepositdate2019-12-05en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorBick, Debra|en_UK
local.rioxx.authorTaylor, Cath|en_UK
local.rioxx.authorBhavnani, Vanita|en_UK
local.rioxx.authorHealey, Andy|en_UK
local.rioxx.authorSeed, Paul|en_UK
local.rioxx.authorRoberts, Sarah|en_UK
local.rioxx.authorZasada, Magdelena|en_UK
local.rioxx.authorAvery, Amanda|en_UK
local.rioxx.authorCraig, Victoria|en_UK
local.rioxx.authorKhazaezadah, Nina|en_UK
local.rioxx.authorMcMullen, Sarah|en_UK
local.rioxx.authorO’Connor, Sheila|en_UK
local.rioxx.authorOki, Bimpi|en_UK
local.rioxx.authorOteng Ntim, Eugene|en_UK
local.rioxx.authorPoston, Lucilla|en_UK
local.rioxx.authorUssher, Michael|0000-0002-0995-7955en_UK
local.rioxx.projectProject ID unknown|National Institute for Health Research|http://dx.doi.org/10.13039/501100000272en_UK
local.rioxx.freetoreaddate2020-12-06en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved||2020-12-05en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2020-12-06|en_UK
local.rioxx.filename1471-0528.16043.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1471-0528en_UK
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