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Online Data Collection to Evaluate a Theoretical Cognitive Model of Tinnitus

Handscomb, Lucy; Hall, Deborah A; Shorter, Gillian W; Hoare, Derek J

Description

Purpose The purpose of this article is to describe data collection considerations, methods, and response rates for a survey available both online and on paper. Methodological issues in the design of online data collection, and advantages and disadvantages of different data collection methods are discussed. Method A survey was compiled that included 9 full or partial clinical questionnaires designed to measure different components relevant to tinnitus distress. It was completed once by 342...[Show more]

dc.contributor.authorHandscomb, Lucy
dc.contributor.authorHall, Deborah A
dc.contributor.authorShorter, Gillian W
dc.contributor.authorHoare, Derek J
dc.date.accessioned2017-04-03T06:15:31Z
dc.date.available2017-04-03T06:15:31Z
dc.identifier.issn1059-0889
dc.identifier.urihttp://hdl.handle.net/1885/114367
dc.description.abstractPurpose The purpose of this article is to describe data collection considerations, methods, and response rates for a survey available both online and on paper. Methodological issues in the design of online data collection, and advantages and disadvantages of different data collection methods are discussed. Method A survey was compiled that included 9 full or partial clinical questionnaires designed to measure different components relevant to tinnitus distress. It was completed once by 342 members of the public with tinnitus. Respondents could choose whether to complete the survey online or on paper. Results Ninety-five percent of participants chose to complete the survey online. The advantages of an online self-administered questionnaire include low numbers of unanswered questions, convenience (particularly in a longer survey such as this), a fast return rate, and reduced expense. Age emerged as an important variable, with those opting to complete the paper-based version of the survey being older. Conclusions Online data collection has several advantages to both participants and researchers. However, cross-sectional studies such as that presented here should also offer paper questionnaires to avoid excluding certain subgroups of the population. Ethics and reporting guidelines for Internet-delivered questionnaire studies are available. These can usefully inform study design and guide high-quality reporting.
dc.description.sponsorshipLucy Handscomb was funded by the British Tinnitus Asso-ciation. Deborah A. Hall and Derek J. Hoare were funded bythe Nat ional Institute for Health Research (NIHR) BiomedicalResearch Unit program.
dc.format.mimetypeapplication/pdf
dc.publisherAmerican Speech-Language-Hearing Association
dc.rights© 2016 The Authors. This work is licensed under a Creative Commons Attribution 4.0 International License.
dc.sourceAmerican journal of audiology
dc.titleOnline Data Collection to Evaluate a Theoretical Cognitive Model of Tinnitus
dc.typeJournal article
local.identifier.citationvolume25
dc.date.issued2016-10-01
local.publisher.urlhttp://www.asha.org/default.htm
local.type.statusPublished Version
local.contributor.affiliationShorter, G. W., National Institute for Mental Health Research, The Australian NationalUniversity
local.identifier.essn1558-9137
local.bibliographicCitation.issue3S
local.bibliographicCitation.startpage313
local.bibliographicCitation.lastpage317
local.identifier.doi10.1044/2016_AJA-16-0007
dcterms.accessRightsOpen Access
CollectionsANU Research Publications

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