Literature DB >> 17904717

Changing constructions of informed consent: qualitative research and complex social worlds.

Tina Miller1, Mary Boulton.   

Abstract

Informed consent is a concept which attempts to capture and convey what is regarded as the appropriate relationship between researcher and research participant. Definitions have traditionally emphasised respect for autonomy and the right to self-determination of the individual. However, the meaning of informed consent and the values on which it is based are grounded in society and the practicalities of social relationships. As society changes, so too do the meaning and practice of informed consent. In this paper, we trace the ways in which the meaning and practice of informed consent has changed over the last 35 years with reference to four qualitative studies of parenting and children in the UK which we have undertaken at different points in our research careers. We focus in particular on the shifting boundaries between the professional and personal, and changing expressions of agency and power in a context of heightened perceptions of risk in everyday life. We also discuss developments in information and communication technologies as a factor in changing both the formal requirements for and the situated practicalities of obtaining informed consent. We conclude by considering the implications for informed consent of both increasing bureaucratic regulation and increasingly sophisticated information and communication technologies and suggest strategies for rethinking and managing 'consent' in qualitative research practice.

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Year:  2007        PMID: 17904717     DOI: 10.1016/j.socscimed.2007.08.009

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  6 in total

1.  How IRBs view and make decisions about consent forms.

Authors:  Robert L Klitzman
Journal:  J Empir Res Hum Res Ethics       Date:  2013-02       Impact factor: 1.742

2.  Accessing health services through the back door: a qualitative interview study investigating reasons why people participate in health research in Canada.

Authors:  Anne Townsend; Susan M Cox
Journal:  BMC Med Ethics       Date:  2013-10-12       Impact factor: 2.652

3.  Informed Consent in Asymmetrical Relationships: an Investigation into Relational Factors that Influence Room for Reflection.

Authors:  Shannon Lydia Spruit; Ibo van de Poel; Neelke Doorn
Journal:  Nanoethics       Date:  2016-05-24       Impact factor: 0.917

4.  Conducting focus groups in neurodegenerative disease populations: ethical and methodological considerations.

Authors:  Annabel Jones; Philippa Morgan-Jones; Monica Busse; Victoria Shepherd; Fiona Wood
Journal:  BMJ Open       Date:  2021-01-13       Impact factor: 3.006

5.  Securing recruitment and obtaining informed consent in minority ethnic groups in the UK.

Authors:  Cathy E Lloyd; Mark R D Johnson; Shanaz Mughal; Jackie A Sturt; Gary S Collins; Tapash Roy; Rukhsana Bibi; Anthony H Barnett
Journal:  BMC Health Serv Res       Date:  2008-03-30       Impact factor: 2.655

6.  Ethical Considerations and Dilemmas Before, during and after Fieldwork in Less-Democratic Contexts: some Reflections from Post-Uprising Egypt.

Authors:  Arne F Wackenhut
Journal:  Am Sociol       Date:  2017-08-19
  6 in total

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