JME

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
[Advanced]

Journal of Medical Ethics 2005;31:715-720; doi:10.1136/jme.2003.003228
Copyright © 2005 by the BMJ Publishing Group Ltd & Institute of Medical Ethics.

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this link to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Burke, T M
Right arrow Articles by Zlotkin, S
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Burke, T M
Right arrow Articles by Zlotkin, S

RESEARCH ETHICS

Children’s understanding of the risks and benefits associated with research

T M Burke1, R Abramovitch2, S Zlotkin3

1 Department of Psychology, Ryerson University, Toronto, Ontario, Canada
2 Department of Psychology, University of Toronto, Toronto, Ontario, Canada
3 Departments of Paediatrics and Nutritional Sciences, University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada

Correspondence to:
Tara M Burke
Department of Psychology, Ryerson University, 350 Victoria Street, Toronto, Ontario, M5B 2K3, Canada; tburke{at}ryerson.ca Objective: The objective of the current study was to maximise the amount of information children and adolescents understand about the risks and benefits associated with participation in a biomedical research study.

Design: Participants were presented with one of six hypothetical research protocols describing how to fix a fractured thigh using either a "standard" cast or "new" pins procedure. Risks and benefits associated with each of the treatment options were manipulated so that for each one of the six protocols there was either a correct or ambiguous choice.

Participants and setting: Two hundred and fifty one children, ages 6–15 (53% boys), and 237 adults (30% men) were interviewed while waiting for a clinic appointment at the Hospital for Sick Children.

Results: Using standardised procedures and questionnaires, it was determined that most participants, regardless of age group, were able to understand the basic purpose and procedures involved in the research, and most were able to choose the "correct" operation. The younger children, however, showed an overall preference for a cast operation, whereas the older participants were more likely to choose the pins.

Conclusions: By creating age appropriate modules of information, children as young as six years can understand potentially difficult and complex concepts such as the risks and benefits associated with participation in biomedical research. It appears, however, that different criteria were used for treatment preference, regardless of associated risks; older participants tended to opt for mobility (the pins procedure) whereas younger participants stayed with the more familiar cast operation.


Keywords: children; biomedical research; ethics; assent; risks; benefits




This article has been cited by other articles:


Home page
West J Nurs ResHome page
B. Holaday, O. Gonzales, and D. Mills
Assent of School-Age Bilingual Children
West J Nurs Res, June 1, 2007; 29(4): 466 - 485.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 2005 by the BMJ Publishing Group Ltd & Institute of Medical Ethics.