Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/18368
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dc.contributor.authorEricson, Jennyen_UK
dc.contributor.authorEriksson, Matsen_UK
dc.contributor.authorHellstrom-Westas, Lenaen_UK
dc.contributor.authorHagberg, Larsen_UK
dc.contributor.authorHoddinott, Paten_UK
dc.contributor.authorFlacking, Reneeen_UK
dc.date.accessioned2014-09-13T20:58:49Z-
dc.date.available2014-09-13T20:58:49Z-
dc.date.issued2013-05-10en_UK
dc.identifier.other73en_UK
dc.identifier.urihttp://hdl.handle.net/1893/18368-
dc.description.abstractBackground: Although breast milk has numerous benefits for infants' development, with greater effects in those born preterm (at < 37 gestational weeks), mothers of preterm infants have shorter breastfeeding duration than mothers of term infants. One of the explanations proposed is the difficulties in the transition from a Neonatal Intensive Care Unit (NICU) to the home environment. A person-centred proactive telephone support intervention after discharge from NICU is expected to promote mothers' sense of trust in their own capacity and thereby facilitate breastfeeding. Methods/design: A multicentre randomized controlled trial has been designed to evaluate the effectiveness and cost-effectiveness of person-centred proactive telephone support on breastfeeding outcomes for mothers of preterm infants. Participating mothers will be randomized to either an intervention group or control group. In the intervention group person-centred proactive telephone support will be provided, in which the support team phones the mother daily for up to 14 days after hospital discharge. In the control group, mothers are offered a person-centred reactive support where mothers can phone the breastfeeding support team up to day 14 after hospital discharge. The intervention group will also be offered the same reactive telephone support as the control group. A stratified block randomization will be used; group allocation will be by high or low socioeconomic status and by NICU. Recruitment will be performed continuously until 1116 mothers (I: 558 C: 558) have been included. Primary outcome: proportion of mothers exclusively breastfeeding at eight weeks after discharge. Secondary outcomes: proportion of breastfeeding (exclusive, partial, none and method of feeding), mothers satisfaction with breastfeeding, attachment, stress and quality of life in mothers/partners at eight weeks after hospital discharge and at six months postnatal age. Data will be collected by researchers blind to group allocation for the primary outcome. A qualitative evaluation of experiences of receiving/providing the intervention will also be undertaken with mothers and staff. Discussion: This paper presents the rationale, study design and protocol for a RCT providing person-centred proactive telephone support to mothers of preterm infants. Furthermore, with a health economic evaluation, the cost-effectiveness of the intervention will be assessed.en_UK
dc.language.isoenen_UK
dc.publisherBioMed Central Ltden_UK
dc.relationEricson J, Eriksson M, Hellstrom-Westas L, Hagberg L, Hoddinott P & Flacking R (2013) The effectiveness of proactive telephone support provided to breastfeeding mothers of preterm infants: Study protocol for a randomized controlled trial. BMC Pediatrics, 13 (1), Art. No.: 73. https://doi.org/10.1186/1471-2431-13-73en_UK
dc.rights© 2013 Ericson et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted 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.subjectBreastfeedingen_UK
dc.subjectMothersen_UK
dc.subjectNeonatal careen_UK
dc.subjectPreterm infanten_UK
dc.subjectSupporten_UK
dc.subjectTelephoneen_UK
dc.titleThe effectiveness of proactive telephone support provided to breastfeeding mothers of preterm infants: Study protocol for a randomized controlled trialen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1186/1471-2431-13-73en_UK
dc.citation.jtitleBMC Pediatricsen_UK
dc.citation.issn1471-2431en_UK
dc.citation.volume13en_UK
dc.citation.issue1en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.author.emailp.m.hoddinott@stir.ac.uken_UK
dc.contributor.affiliationUppsala Universityen_UK
dc.contributor.affiliationOrebro Universityen_UK
dc.contributor.affiliationUppsala Universityen_UK
dc.contributor.affiliationOrebro Universityen_UK
dc.contributor.affiliationHealth Sciences Research - Stirling - LEGACYen_UK
dc.contributor.affiliationUniversity of Central Lancashireen_UK
dc.identifier.isiWOS:000318953500001en_UK
dc.identifier.scopusid2-s2.0-84877291737en_UK
dc.identifier.wtid665205en_UK
dc.contributor.orcid0000-0002-4372-9681en_UK
dc.date.accepted2013-05-02en_UK
dcterms.dateAccepted2013-05-02en_UK
dc.date.filedepositdate2014-01-20en_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorEricson, Jenny|en_UK
local.rioxx.authorEriksson, Mats|en_UK
local.rioxx.authorHellstrom-Westas, Lena|en_UK
local.rioxx.authorHagberg, Lars|en_UK
local.rioxx.authorHoddinott, Pat|0000-0002-4372-9681en_UK
local.rioxx.authorFlacking, Renee|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2014-01-20en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2014-01-20|en_UK
local.rioxx.filenameBMC Pediatrics 2013 Sweden FEST.pdfen_UK
local.rioxx.filecount1en_UK
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