431
Views
3
CrossRef citations to date
0
Altmetric
ARTICLES

Ethical Issues in Researching Black Teenage Mothers with Harmful Childhood Histories: Marginal Voices

Pages 54-73 | Received 08 Feb 2012, Accepted 11 Feb 2012, Published online: 12 Mar 2012
 

Abstract

This paper highlights a number of ethical dilemmas encountered in a pilot study with a hard-to-reach group of research participants with harmful childhood histories. Drawing on a project exploring black teenage mothers' understandings of their own childhood experiences of abuse, it is argued that in asking young mothers to talk about such an emotionally sensitive topic as their own harmful childhood, a number of challenges are posed about how to deal with number of key ethical principles. The paper begins by outlining the context of the pilot study, including the research literature on this subject. It then discusses three key ethical principles that were considered during the process of the research: issues of gaining consent; and when the principle of confidentiality ought to be breached when a duty of care prerogative emerges. The paper explores these tensions in operationalising these principles when dealing with the competing needs and rights of gatekeepers, the young women and their carers, using occasional extracts from research findings to illustrate these tensions. The paper concludes with a discussion of the ethical challenges in accessing marginal voices in social research.

Acknowledgements

The author wishes to thank BASPCAN for the funding for this project. The author also thanks the anonymous reviewers and Professor Jim Campbell for their helpful feedback on earlier drafts of this paper.

Notes

1This competency is used to consider the ability of children and young people under the age of 16 to give informed consent. It originally addressed the question of the rights of children/young people under the age of 16 to consent to treatment on their own behalf and was reviewed by the courts in 1985, in connection with contraception. This principle has been extended beyond consent to medical treatment and has been used in subsequent legislation, for example the Children Act (1989).

Additional information

Notes on contributors

Claudia Bernard

Claudia Bernard is Head of Postgraduate Studies in the Department of Professional and Community Education at Goldsmiths, University of London. Her research interests lie in investigating the intersection of race, gender, social class, and child and family welfare

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 53.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 241.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.