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dc.contributor.authorStarr, Kathryn
dc.contributor.authorMcPherson, Gladys
dc.contributor.authorForrest, Mark
dc.contributor.authorCotton, Seonaidh C.
dc.date.accessioned2015-10-20T09:09:01Z
dc.date.available2015-10-20T09:09:01Z
dc.date.issued2015-07-08
dc.identifier57706312
dc.identifiera7cbe8a9-c258-4390-aab0-f99c7437dbab
dc.identifier000357562000001
dc.identifier84935480802
dc.identifier.citationStarr , K , McPherson , G , Forrest , M & Cotton , S C 2015 , ' SMS text pre-notification and delivery of reminder e-mails to increase response rates to postal questionnaires in the SUSPEND trial : a factorial design, randomised controlled trial ' , Trials , vol. 16 , 295 . https://doi.org/10.1186/s13063-015-0808-9en
dc.identifier.issn1745-6215
dc.identifier.urihttp://hdl.handle.net/2164/5080
dc.descriptionAcknowledgements SUSPEND was funded by the National Institute for Health Research (NIHR) Health Technology Assessment (HTA) Programme (project 80/71/01) and will be published in full in Health Technology Assessment. The Health Services Research Unit of the University of Aberdeen is funded in part by the Chief Scientist Office of the Scottish Government Health and Social Care Directorates. The views and opinions expressed herein are those of the authors and do not necessarily reflect those of the Chief Scientist Office, HTA programme, NIHR, National Health Service, or Department of Health. The authors thank the SUSPEND staff and participants, without whom this study would not have been possible.en
dc.format.extent8
dc.format.extent877855
dc.language.isoeng
dc.relation.ispartofTrialsen
dc.subjectQuestionnairesen
dc.subjectNon-responseen
dc.subjectRandomised controlled trialen
dc.subjectShort messenger service (SMS)en
dc.subjectElectronic mail (e-mail)en
dc.subjectRETENTIONen
dc.subjectCOHORTen
dc.subjectNational Institute for Health Research (NIHR)en
dc.subject80/71/01en
dc.titleSMS text pre-notification and delivery of reminder e-mails to increase response rates to postal questionnaires in the SUSPEND trial : a factorial design, randomised controlled trialen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Health Services Research Uniten
dc.contributor.institutionUniversity of Aberdeen.Academic Urology Uniten
dc.contributor.institutionUniversity of Aberdeen.Institute of Applied Health Sciencesen
dc.description.statusPeer revieweden
dc.identifier.doi10.1186/s13063-015-0808-9
dc.identifier.vol16en


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