The use of social networks in scientific research with questionnaires

dc.creatorSoraya de Mattos Camargo Grossmann
dc.creatorMariela Dutra Gontijo de Moura
dc.creatorMichelle Danielle Porto Matias
dc.creatorSaul Martins de Paiva
dc.creatorRicardo Alves de Mesquita
dc.date.accessioned2025-07-04T20:32:39Z
dc.date.accessioned2025-09-09T01:12:07Z
dc.date.available2025-07-04T20:32:39Z
dc.date.issued2018-07-10
dc.format.mimetypepdf
dc.identifier.doihttp://dx.doi.org/10.20396/bjos.v17i0.8652908
dc.identifier.issn1677-3225
dc.identifier.urihttps://hdl.handle.net/1843/83346
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofBrazilian Journal of Oral Sciences
dc.rightsAcesso Aberto
dc.subjectEpidermolysis bullosa
dc.subjectElectronic mail
dc.subjectQuality of life
dc.subjectSocial support
dc.subjectSurveys and questionnaires
dc.subjectCaregivers
dc.subjectSocial networking
dc.subject.otherEpidermolysis bullosa
dc.subject.otherElectronic mail
dc.subject.otherQuality of life
dc.subject.otherSocial support
dc.subject.otherSurveys and questionnaires
dc.titleThe use of social networks in scientific research with questionnaires
dc.typeArtigo de periódico
local.citation.epage8
local.citation.spage1
local.citation.volume17
local.description.resumoAim: The aim of this study was to determine the response rate of the SF-36 quality of life questionnaire sent and received by mail and over a social network to caregivers of individuals with epidermolysis bullosa (EB) in Brazil. Methods: All volunteers were first-degree relatives of patients with EB that directly spent time helping them with their basic activities of daily living. A maximum of two caregivers per patient could answer the questionnaire. Volunteers were divided into two groups: for group 1, questionnaires were sent to 53 members of a support association for the disease by mail, and for group 2, 798 members of the Facebook™ page of friends and relatives of patients with EB were invited to participate using an access link to Google Drive™ to gain access to the questionnaire. The data from both groups were analyzed 150 days after the start the study. Descriptive analysis was performed by EpiInfo8 and the return of questionnaires was evaluated according to age, sex, and time of return using the Chi-squared and Fisher’s exact test. Results: After 150 days, 30 questionnaires were returned, 17 (56.7%) of which from group 1 and 13 (43.3%) from group 2. Approximately 12 questionnaires were returned by mail and 11 over the social network. Conclusions: The data collection of the SF-36 quality of life questionnaire from caregivers of individuals with EB over a social network seems to be efficient mainly when it is necessary to collect results within a short timeframe, highlighting the importance of social networks as a means for conducting this type of research. However, in our study, the most efficient method was distributing the questionnaires by mail.Keywords: Epidermolysis bullosa. Electronic mail. Quality of life. Social support. Surveys and questionnaires.
local.identifier.orcidhttps://orcid.org/0000-0002-8920-3853
local.identifier.orcidhttps://orcid.org/0000-0003-3576-3457
local.identifier.orcidhttps://orcid.org/0000-0002-8598-4170
local.identifier.orcidhttps://orcid.org/0000-0002-3968-1638
local.identifier.orcidhttps://orcid.org/0000-0003-3207-4007
local.publisher.countryBrasil
local.publisher.departmentFAO - DEPARTAMENTO DE CLÍNICA
local.publisher.departmentFAO - DEPARTAMENTO DE ODONTOPEDIATRIA E ORTODONTIA
local.publisher.initialsUFMG
local.url.externahttps://periodicos.sbu.unicamp.br/ojs/index.php/bjos/article/view/8652908

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