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dc.contributor.authorClarkson, Jan E.
dc.contributor.authorPitts, Nigel B.
dc.contributor.authorBonetti, Debbie
dc.contributor.authorBoyers, Dwayne
dc.contributor.authorBraid, Hazel
dc.contributor.authorElford, Robert
dc.contributor.authorFee, Patrick A.
dc.contributor.authorFloate, Ruth
dc.contributor.authorGoulão, Beatriz
dc.contributor.authorHumphris, Gerry
dc.contributor.authorNeedleman, Ian
dc.contributor.authorNorrie, John D. T.
dc.contributor.authorOrd, Fiona
dc.contributor.authorvan der Pol, Marjon
dc.contributor.authorRamsay, Craig R.
dc.contributor.authorRicketts, David N. J.
dc.contributor.authorWorthington, Helen V.
dc.contributor.authorYoung, Linda
dc.contributor.authorAnderson, Tony
dc.contributor.authorBurke, Trevor
dc.contributor.authorDolan, Philip
dc.contributor.authorDouglas, Gail
dc.contributor.authorFreeman, Ruth
dc.contributor.authorGorter, Ronald
dc.contributor.authorHerbert, Richard
dc.contributor.authorHodge, Penny
dc.contributor.authorMettes, Dirk
dc.contributor.authorMcCombes, Wendy
dc.contributor.authorRoss, Margaret
dc.contributor.authorWhite, Debbie
dc.contributor.authorINTERVAL Trial Collaboration
dc.date.accessioned2018-08-09T13:30:05Z
dc.date.available2018-08-09T13:30:05Z
dc.date.issued2018-08-07
dc.identifier255238157
dc.identifier842c24d9-6124-415f-ae07-cc0ddf26fcc7
dc.identifier85058839781
dc.identifier000441213800003
dc.identifier.citationClarkson , J E , Pitts , N B , Bonetti , D , Boyers , D , Braid , H , Elford , R , Fee , P A , Floate , R , Goulão , B , Humphris , G , Needleman , I , Norrie , J D T , Ord , F , van der Pol , M , Ramsay , C R , Ricketts , D N J , Worthington , H V , Young , L , Anderson , T , Burke , T , Dolan , P , Douglas , G , Freeman , R , Gorter , R , Herbert , R , Hodge , P , Mettes , D , McCombes , W , Ross , M , White , D & INTERVAL Trial Collaboration 2018 , ' INTERVAL (investigation of NICE technologies for enabling risk-variable-adjusted-length) dental recalls trial : a multicentre randomised controlled trial investigating the best dental recall interval for optimum, cost-effective maintenance of oral health in dentate adults attending dental primary care ' , BMC Oral Health , vol. 18 , 135 . https://doi.org/10.1186/s12903-018-0587-2en
dc.identifier.issn1472-6831
dc.identifier.otherRIS: urn:EB2EA92FFBAAF0A755DDB796D5AFE26A
dc.identifier.otherRIS: Clarkson2018
dc.identifier.otherORCID: /0000-0002-4601-8834/work/64033879
dc.identifier.urihttps://hdl.handle.net/10023/15791
dc.descriptionThis project was funded by the National Institute for Health Research Health Technology Assessment (NIHR HTA) Programme (project number 06/35/99) and will be published in full in Health Technology Assessment.en
dc.description.abstractBackground:  Traditionally, patients at low risk and high risk of developing dental disease have been encouraged to attend dental recall appointments at regular intervals of six months between appointments. The lack of evidence for the effect that different recall intervals between dental check-ups have on patient outcomes, provider workload and healthcare costs is causing considerable uncertainty for the profession and patients, despite the publication of the NICE Guideline on dental recall. The need for primary research has been highlighted in the Health Technology Assessment Group’s systematic review of routine dental check-ups, which found little evidence to support or refute the practice of encouraging 6-monthly dental check-ups in adults. The more recent Cochrane review on recall interval concluded there was insufficient evidence to draw any conclusions regarding the potential beneficial or harmful effects of altering the recall interval between dental check-ups. There is therefore an urgent need to assess the relative effectiveness and cost-benefit of different dental recall intervals in a robust, sufficiently powered randomised control trial (RCT) in primary dental care. Methods: This is a four year multi-centre, parallel-group, randomised controlled trial with blinded outcome assessment based in dental primary care in the UK. Practitioners will recruit 2372 dentate adult patients. Patient participants will be randomised to one of three groups: fixed-period six month recall, risk-based recall, or fixed-period twenty-four month recall. Outcome data will be assessed through clinical examination, patient questionnaires and NHS databases. The primary outcomes measure gingival inflammation/bleeding on probing and oral health-related quality of life. Discussion: INTERVAL will provide evidence for the most clinically-effective and cost-beneficial recall interval for maintaining optimum oral health in dentate adults attending general dental practice.
dc.format.extent10
dc.format.extent1027084
dc.language.isoeng
dc.relation.ispartofBMC Oral Healthen
dc.subjectDental recallen
dc.subjectOral healthen
dc.subjectRCTen
dc.subjectPrimary careen
dc.subjectRK Dentistryen
dc.subjectT-NDASen
dc.subject.lccRKen
dc.titleINTERVAL (investigation of NICE technologies for enabling risk-variable-adjusted-length) dental recalls trial : a multicentre randomised controlled trial investigating the best dental recall interval for optimum, cost-effective maintenance of oral health in dentate adults attending dental primary careen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. Population and Behavioural Science Divisionen
dc.contributor.institutionUniversity of St Andrews. WHO Collaborating Centre for International Child & Adolescent Health Policyen
dc.contributor.institutionUniversity of St Andrews. Health Psychologyen
dc.contributor.institutionUniversity of St Andrews. St Andrews Sustainability Instituteen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.identifier.doi10.1186/s12903-018-0587-2
dc.description.statusPeer revieweden


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