Show simple item record

dc.contributor.authorFenlon, D
dc.contributor.authorNuttall, J
dc.contributor.authorMay, C
dc.contributor.authorRaftery, J
dc.contributor.authorFields, J
dc.contributor.authorKirkpatrick, E
dc.contributor.authorAbab, J
dc.contributor.authorEllis, M
dc.contributor.authorRose, T
dc.contributor.authorKhambhaita, P
dc.contributor.authorGalanopoulou, A
dc.contributor.authorMaishman, T
dc.contributor.authorHaviland, J
dc.contributor.authorGriffiths, G
dc.contributor.authorTurner, L
dc.contributor.authorHunter, M
dc.date.accessioned2018-05-22T08:04:42Z
dc.date.issued2018-05-08
dc.identifier.citationBMC women's health, 2018, 18 (1), pp. 63 - ?
dc.identifier.issn1472-6874
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1678
dc.identifier.eissn1472-6874
dc.identifier.doi10.1186/s12905-018-0550-z
dc.description.abstractBACKGROUND: Women who have been treated for breast cancer may identify vasomotor symptoms, such as hot flushes and night sweats (HFNS), as a serious problem. HFNS are unpleasant to experience and can have a significant impact on daily life, potentially leading to reduced adherence to life saving adjuvant hormonal therapy. It is known that Cognitive Behavioural Therapy (CBT) is effective for the alleviation of hot flushes in both well women and women who have had breast cancer. Most women with breast cancer will see a breast care nurse and there is evidence that nurses can be trained to deliver psychological treatments to a satisfactory level, whilst also maintaining treatment fidelity. The research team will assess whether breast care nurses can effectively deliver a CBT intervention to alleviate hot flushes in women with breast cancer. METHODS: This study is a multi-centre phase III individually randomised controlled trial of group CBT versus usual care to reduce the impact of hot flushes in women with breast cancer. 120-160 women with primary breast cancer experiencing seven or more problematic HFNS a week will be randomised to receive either treatment as usual (TAU) or participation in the group CBT intervention plus TAU (CBT Group). A process evaluation using May's Normalisation Process Theory will be conducted, as well as practical and organisational issues relating to the implementation of the intervention. Fidelity of implementation of the intervention will be conducted by expert assessment. The cost effectiveness of the intervention will also be assessed. DISCUSSION: There is a need for studies that enable effective interventions to be implemented in practice. There is good evidence that CBT is helpful for women with breast cancer who experience HFNS, yet it is not widely available. It is not yet known whether the intervention can be effectively delivered by breast care nurses or implemented in practice. This study will provide information on both whether the intervention can effectively help women with hot flushes and whether and how it can be translated into routine clinical practice. TRIAL REGISTRATION: ISRCTN 12824632 . Registered 25-01-2017.
dc.formatElectronic
dc.format.extent63 - ?
dc.languageeng
dc.language.isoeng
dc.publisherBIOMED CENTRAL LTD
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectHot Flashes
dc.subjectPsychotherapy, Group
dc.subjectSweating
dc.subjectResearch Design
dc.subjectCost-Benefit Analysis
dc.subjectFemale
dc.subjectPractice Patterns, Nurses'
dc.subjectCognitive Behavioral Therapy
dc.titleMENOS4 trial: a multicentre randomised controlled trial (RCT) of a breast care nurse delivered cognitive behavioural therapy (CBT) intervention to reduce the impact of hot flushes in women with breast cancer: Study Protocol.
dc.typeJournal Article
dcterms.dateAccepted2018-04-10
rioxxterms.versionofrecord10.1186/s12905-018-0550-z
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-05-08
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBMC women's health
pubs.issue1
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.publication-statusPublished
pubs.volume18
pubs.embargo.termsNot known
icr.researchteamClinical Trials & Statistics Unit
dc.contributor.icrauthorHaviland, Joanne


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by/4.0
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0