'You don't know which bits to believe'

qualitative study exploring carers' experiences of seeking information on the internet about childhood eczema

Miriam Santer (Lead / Corresponding author), Ingrid Muller, Lucy Yardley, Hana Burgess, Steven J. Ersser, Sue Lewis-Jones, Paul Little

    Research output: Contribution to journalArticle

    13 Citations (Scopus)

    Abstract

    OBJECTIVE: We sought to explore parents and carers' experiences of searching for information about childhood eczema on the internet.

    DESIGN: A qualitative interview study was carried out among carers of children aged 5 years or less with a recorded diagnosis of eczema. The main focus of the study was to explore carers' beliefs and understandings around eczema and its treatment. As part of this, we explored experiences of formal and informal information seeking about childhood eczema. Transcripts of interviews were analysed thematically.

    SETTING: Participants were recruited from six general practices in South West England.

    PARTICIPANTS: Interviews were carried out with 31 parents from 28 families.

    RESULTS: Experiences of searching for eczema information on the internet varied widely. A few interviewees were able to navigate through the internet and find the specific information they were looking for (for instance about treatments their child had been prescribed), but more found searching for eczema information online to be a bewildering experience. Some could find no information of relevance to them, whereas others found the volume of different information sources overwhelming. Some said that they were unsure how to evaluate online information or that they were wary of commercial interests behind some information sources. Interviewees said that they would welcome more signposting towards high quality information from their healthcare providers.

    CONCLUSIONS: We found very mixed experiences of seeking eczema information on the internet; but many participants in this study found this to be frustrating and confusing. Healthcare professionals and healthcare systems have a role to play in helping people with long-term health conditions and their carers find reliable online information to support them with self-care.

    Original languageEnglish
    Article numbere006339
    Number of pages6
    JournalBMJ Open
    Volume5
    Issue number4
    DOIs
    Publication statusPublished - 8 Apr 2015

    Fingerprint

    Eczema
    Internet
    Caregivers
    Interviews
    Parents
    Delivery of Health Care
    Self Care
    General Practice
    England
    Health Personnel
    Health
    Therapeutics

    Cite this

    Santer, Miriam ; Muller, Ingrid ; Yardley, Lucy ; Burgess, Hana ; Ersser, Steven J. ; Lewis-Jones, Sue ; Little, Paul. / 'You don't know which bits to believe' : qualitative study exploring carers' experiences of seeking information on the internet about childhood eczema. In: BMJ Open. 2015 ; Vol. 5, No. 4.
    @article{1494b36abb304904b8d17715516da59d,
    title = "'You don't know which bits to believe': qualitative study exploring carers' experiences of seeking information on the internet about childhood eczema",
    abstract = "OBJECTIVE: We sought to explore parents and carers' experiences of searching for information about childhood eczema on the internet.DESIGN: A qualitative interview study was carried out among carers of children aged 5 years or less with a recorded diagnosis of eczema. The main focus of the study was to explore carers' beliefs and understandings around eczema and its treatment. As part of this, we explored experiences of formal and informal information seeking about childhood eczema. Transcripts of interviews were analysed thematically.SETTING: Participants were recruited from six general practices in South West England.PARTICIPANTS: Interviews were carried out with 31 parents from 28 families.RESULTS: Experiences of searching for eczema information on the internet varied widely. A few interviewees were able to navigate through the internet and find the specific information they were looking for (for instance about treatments their child had been prescribed), but more found searching for eczema information online to be a bewildering experience. Some could find no information of relevance to them, whereas others found the volume of different information sources overwhelming. Some said that they were unsure how to evaluate online information or that they were wary of commercial interests behind some information sources. Interviewees said that they would welcome more signposting towards high quality information from their healthcare providers.CONCLUSIONS: We found very mixed experiences of seeking eczema information on the internet; but many participants in this study found this to be frustrating and confusing. Healthcare professionals and healthcare systems have a role to play in helping people with long-term health conditions and their carers find reliable online information to support them with self-care.",
    author = "Miriam Santer and Ingrid Muller and Lucy Yardley and Hana Burgess and Ersser, {Steven J.} and Sue Lewis-Jones and Paul Little",
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    year = "2015",
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    doi = "10.1136/bmjopen-2014-006339",
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    'You don't know which bits to believe' : qualitative study exploring carers' experiences of seeking information on the internet about childhood eczema. / Santer, Miriam (Lead / Corresponding author); Muller, Ingrid; Yardley, Lucy; Burgess, Hana; Ersser, Steven J.; Lewis-Jones, Sue; Little, Paul.

    In: BMJ Open, Vol. 5, No. 4, e006339, 08.04.2015.

    Research output: Contribution to journalArticle

    TY - JOUR

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    T2 - qualitative study exploring carers' experiences of seeking information on the internet about childhood eczema

    AU - Santer, Miriam

    AU - Muller, Ingrid

    AU - Yardley, Lucy

    AU - Burgess, Hana

    AU - Ersser, Steven J.

    AU - Lewis-Jones, Sue

    AU - Little, Paul

    N1 - Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

    PY - 2015/4/8

    Y1 - 2015/4/8

    N2 - OBJECTIVE: We sought to explore parents and carers' experiences of searching for information about childhood eczema on the internet.DESIGN: A qualitative interview study was carried out among carers of children aged 5 years or less with a recorded diagnosis of eczema. The main focus of the study was to explore carers' beliefs and understandings around eczema and its treatment. As part of this, we explored experiences of formal and informal information seeking about childhood eczema. Transcripts of interviews were analysed thematically.SETTING: Participants were recruited from six general practices in South West England.PARTICIPANTS: Interviews were carried out with 31 parents from 28 families.RESULTS: Experiences of searching for eczema information on the internet varied widely. A few interviewees were able to navigate through the internet and find the specific information they were looking for (for instance about treatments their child had been prescribed), but more found searching for eczema information online to be a bewildering experience. Some could find no information of relevance to them, whereas others found the volume of different information sources overwhelming. Some said that they were unsure how to evaluate online information or that they were wary of commercial interests behind some information sources. Interviewees said that they would welcome more signposting towards high quality information from their healthcare providers.CONCLUSIONS: We found very mixed experiences of seeking eczema information on the internet; but many participants in this study found this to be frustrating and confusing. Healthcare professionals and healthcare systems have a role to play in helping people with long-term health conditions and their carers find reliable online information to support them with self-care.

    AB - OBJECTIVE: We sought to explore parents and carers' experiences of searching for information about childhood eczema on the internet.DESIGN: A qualitative interview study was carried out among carers of children aged 5 years or less with a recorded diagnosis of eczema. The main focus of the study was to explore carers' beliefs and understandings around eczema and its treatment. As part of this, we explored experiences of formal and informal information seeking about childhood eczema. Transcripts of interviews were analysed thematically.SETTING: Participants were recruited from six general practices in South West England.PARTICIPANTS: Interviews were carried out with 31 parents from 28 families.RESULTS: Experiences of searching for eczema information on the internet varied widely. A few interviewees were able to navigate through the internet and find the specific information they were looking for (for instance about treatments their child had been prescribed), but more found searching for eczema information online to be a bewildering experience. Some could find no information of relevance to them, whereas others found the volume of different information sources overwhelming. Some said that they were unsure how to evaluate online information or that they were wary of commercial interests behind some information sources. Interviewees said that they would welcome more signposting towards high quality information from their healthcare providers.CONCLUSIONS: We found very mixed experiences of seeking eczema information on the internet; but many participants in this study found this to be frustrating and confusing. Healthcare professionals and healthcare systems have a role to play in helping people with long-term health conditions and their carers find reliable online information to support them with self-care.

    U2 - 10.1136/bmjopen-2014-006339

    DO - 10.1136/bmjopen-2014-006339

    M3 - Article

    VL - 5

    JO - BMJ Open

    JF - BMJ Open

    SN - 2044-6055

    IS - 4

    M1 - e006339

    ER -