Lay perceptions of evidence-based information – a qualitative evaluation of a website for back pain sufferers

[1]  Alan Irwin,et al.  Misunderstanding science?: Science and Hell's kitchen: the local understanding of hazard issues , 1996 .

[2]  Elizabeth Sillence,et al.  Trust and mistrust of online health sites , 2004, CHI.

[3]  Emma Irvin,et al.  Surfing for Back Pain Patients: The Nature and Quality of Back Pain Information on the Internet , 2001, Spine.

[4]  David L. Sackett,et al.  Evidence based medicine: What it is and what it isn't (reprinted from BMJ, vol 312, pg 71-72, 1996) , 2007 .

[5]  D. Nelkin,et al.  An uneasy relationship: the tensions between medicine and the media , 1996, The Lancet.

[6]  S. Wyatt,et al.  'Ignorance is bliss sometimes': constraints on the emergence of the 'informed patient' in the changing landscapes of health information. , 2003, Sociology of health & illness.

[7]  Christian Köhler,et al.  How do consumers search for and appraise health information on the world wide web? Qualitative study using focus groups, usability tests, and in-depth interviews , 2002, BMJ : British Medical Journal.

[8]  C. Glenton,et al.  Developing patient‐centred information for back pain sufferers , 2002, Health expectations : an international journal of public participation in health care and health policy.

[9]  Claire Glenton,et al.  Portals to Wonderland: Health portals lead to confusing information about the effects of health care , 2005, BMC Medical Informatics Decis. Mak..

[10]  B. Wynne,et al.  Misunderstanding science? : the public reconstruction of science and technology , 1996 .

[11]  J. Benbassat,et al.  Patients' preferences for participation in clinical decision making: a review of published surveys. , 1998, Behavioral medicine.

[12]  Kylie A. Williams,et al.  How do Consumers Search for and Appraise Information on Medicines on the Internet? A Qualitative Study Using Focus Groups , 2003, Journal of medical Internet research.

[13]  R A Deyo,et al.  An interactive videodisc program for low back pain patients. , 1996, Health education research.

[14]  B. Wynne,et al.  Misunderstanding science?: Conclusions , 1996 .

[15]  Claire Glenton,et al.  Summaries of findings, descriptions of interventions, and information about adverse effects would make reviews more informative. , 2006, Journal of clinical epidemiology.

[16]  T A Sheldon,et al.  Evidence-Informed Patient Choice: Practical Issues of Involving Patients in Decisions About Health Care Technologies , 1998, International Journal of Technology Assessment in Health Care.

[17]  Jane Ogden,et al.  What's in a name? An experimental study of patients' views of the impact and function of a diagnosis. , 2003, Family practice.

[18]  V. Entwistle,et al.  Health and medical coverage in the UK national press , 1992 .

[19]  F. Griffiths,et al.  The nature of medical evidence and its inherent uncertainty for the clinical consultation: qualitative study , 2005, BMJ : British Medical Journal.

[20]  K. McPherson,et al.  Cancer patients' information needs and information seeking behaviour: in depth interview study , 2000, BMJ : British Medical Journal.

[21]  R. Barbour.  Introducing Focus Groups , 2007 .

[22]  A. Skelton.  Patient education for the millennium: beyond control and emancipation? , 1997, Patient education and counseling.

[23]  Graham R. Gibbs,et al.  Analyzing Qualitative Data , 2014 .

[24]  D. Sackett,et al.  Evidence based medicine: what it is and what it isn't , 1996, BMJ.

[25]  Bruce V. Lewenstein,et al.  Selling Science: How the Press Covers Science and Technology , 1988 .

[26]  J. Kitzinger,et al.  Qualitative Research: Introducing focus groups , 1995 .

[27]  Sue Ziebland,et al.  The importance of being expert: the quest for cancer information on the Internet. , 2004, Social science & medicine.

[28]  S. Ziebland,et al.  What do patients with prostate or breast cancer want from an Internet site? A qualitative study of information needs. , 2004, Patient education and counseling.

[29]  R. Thomson,et al.  Decision aids for people facing health treatment or screening decisions. , 2003, The Cochrane database of systematic reviews.

[30]  V. Entwistle,et al.  Decision aids for people facing health treatment or screening decisions. , 2018, The Cochrane database of systematic reviews.

[31]  C. Glenton.  Chronic back pain sufferers--striving for the sick role. , 2003, Social science & medicine.

[32]  R A Deyo,et al.  Outcome Measures for Low Back Pain Research: A Proposal for Standardized Use , 1998, Spine.

[33]  C. Mulrow,et al.  Systematic Reviews: Rationale for systematic reviews , 1994, BMJ.

[34]  L. Spencer,et al.  Qualitative data analysis for applied policy research , 2002 .

[35]  K. Malterud.  Shared understanding of the qualitative research process. Guidelines for the medical researcher. , 1993, Family practice.

[36]  M W Enkin,et al.  Using anecdotal information in evidence-based health care: heresy or necessity? , 1998, Annals of oncology : official journal of the European Society for Medical Oncology.