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Telling partners about chlamydia: how acceptable are the new technologies?

dc.contributor.authorHopkins, Carol A
dc.contributor.authorTemple-Smith, Meredith J
dc.contributor.authorFairley, Christopher K
dc.contributor.authorPavlin, Natasha L
dc.contributor.authorTomnay, Jane E
dc.contributor.authorParker, Rhian M
dc.contributor.authorBowden, Francis
dc.contributor.authorRussell, Darren B
dc.contributor.authorHocking, Jane S
dc.contributor.authorChen, Marcus Y
dc.date.accessioned2016-01-12T23:42:39Z
dc.date.available2016-01-12T23:42:39Z
dc.date.issued2010-03-09
dc.date.updated2016-02-24T10:20:59Z
dc.description.abstractBACKGROUND Partner notification is accepted as a vital component in the control of chlamydia. However, in reality, many sexual partners of individuals diagnosed with chlamydia are never informed of their risk. The newer technologies of email and SMS have been used as a means of improving partner notification rates. This study explored the use and acceptability of different partner notification methods to help inform the development of strategies and resources to increase the number of partners notified. METHODS Semi-structured telephone interviews were conducted with 40 people who were recently diagnosed with chlamydia from three sexual health centres and two general practices across three Australian jurisdictions. RESULTS Most participants chose to contact their partners either in person (56%) or by phone (44%). Only 17% chose email or SMS. Participants viewed face-to-face as the "gold standard" in partner notification because it demonstrated caring, respect and courage. Telephone contact, while considered insensitive by some, was often valued because it was quick, convenient and less confronting. Email was often seen as less personal while SMS was generally considered the least acceptable method for telling partners. There was also concern that emails and SMS could be misunderstood, not taken seriously or shown to others. Despite these, email and SMS were seen to be appropriate and useful in some circumstances. Letters, both from the patients or from their doctor, were viewed more favourably but were seldom used. CONCLUSION These findings suggest that many people diagnosed with chlamydia are reluctant to use the new technologies for partner notification, except in specific circumstances, and our efforts in developing partner notification resources may best be focused on giving patients the skills and confidence for personal interaction.
dc.description.sponsorshipThe study was funded by the Australian Federal Government Department of Health and Ageing Chlamydia Pilot Program of Targeted Grants.en_AU
dc.identifier.issn1471-2334en_AU
dc.identifier.urihttp://hdl.handle.net/1885/95361
dc.publisherBioMed Central
dc.rights© Hopkins et al. 2010 This article is published under license to 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.
dc.sourceBMC Infectious Diseases
dc.subjectadolescent
dc.subjectadult
dc.subjectaustralia
dc.subjectcell phones
dc.subjectcontact tracing
dc.subjectelectronic mail
dc.subjectfemale
dc.subjecthumans
dc.subjectinterviews as topic
dc.subjectlymphogranuloma venereum
dc.subjectmale
dc.subjectmiddle aged
dc.subjectpatient acceptance of health care
dc.subjectyoung adult
dc.titleTelling partners about chlamydia: how acceptable are the new technologies?
dc.typeJournal article
local.bibliographicCitation.issue1en_AU
local.bibliographicCitation.startpage58en_AU
local.contributor.affiliationHopkins, Carol, Melbourne Sexual Health Centre, Australiaen_AU
local.contributor.affiliationTemple-Smith, M, La Trobe University, Australiaen_AU
local.contributor.affiliationFairley, Christopher K, Melbourne Sexual Health Centre, Australiaen_AU
local.contributor.affiliationPavlin, Natasha, University of Melbourne, Australiaen_AU
local.contributor.affiliationTomnay, Jane, University of Melbourne, Australiaen_AU
local.contributor.affiliationParker, Rhian, College of Medicine, Biology and Environment, CMBE Research School of Population Health, Australian Primary Health Care Research Institute, The Australian National Universityen_AU
local.contributor.affiliationBowden, Francis, College of Medicine, Biology and Environment, CMBE ANU Medical School, ANU Medical School, The Australian National Universityen_AU
local.contributor.affiliationRussell, Darren, La Trobe University, Australiaen_AU
local.contributor.affiliationHocking, Jane S, University of Melbourne, Australiaen_AU
local.contributor.affiliationChen, Marcus Y, University of Melbourne, Australiaen_AU
local.contributor.authoruida177640en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor110309en_AU
local.identifier.ariespublicationu3961986xPUB37en_AU
local.identifier.citationvolume10en_AU
local.identifier.doi10.1186/1471-2334-10-58en_AU
local.identifier.essn1471-2334en_AU
local.identifier.scopusID2-s2.0-77950442547
local.publisher.urlhttp://www.biomedcentral.com/en_AU
local.type.statusPublished Versionen_AU

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