Roy Marsh, Research Fellow, Evidence Adoption Centre, Cambridge.
T: 01223 746161
Dear all
I completely disagree with the last writer. Our approach should be proportionate and take a measured approach to thinking about research.
Student research is undertaken the world over with little expectation that the results will reach the publiv domain. The benefit is to the community of researchers or practitioners through the education of the next generation.
This decision should consider the actual risk posed by the research. An awful lot of research poses no geater risk than the time taken to participate. Any research restricted to interviews, questionnaires or case review for example. So we should be comfortable with residents undertaking such low risk research as part of their learning. This balance would change if the risks were greater e.g. If treatment decisions were to be altered.
Best wishes
Patricia
On 11 Mar 2011 01:12, "Richard Saitz" <[log in to unmask]> wrote:
Seems to me the issue here is not about publication in journals.
When research is done there are risks to participants. Those risks are only
justified if there are benefits (to them or to science). If the research
results are not available to anyone then they cannot benefit anyone (beyond
those in the study). If they cannot benefit anyone else, then the risk of
the study was not justified. (an internationally accepted ethical
principle).
One can make a solid case for peer review (not that it is perfect but it is
difficult to argue that zero review is a better system for vetting
scientific results). But the issue here is not (in my view) publication in
peer review journals. The ethical issue is making the results available
because if that is not done, the risk was not justified (and one could
ask--why was it done if not to share it).
One might imagine doing a study and telling participants---we will do this
study but we will never publish the results. Anywhere. Because we don't
think peer reviewed journals are good. We will keep them secret. Or, we wont
share them because we are too busy to write them down...
Would the participant agree? Should they? Is that ethical? And to return to
the focus of the listserve, what is the impact on systematic reviews that
try to determine the efficacy of interventions when such studies are not
reported? (they become either useless or unknowingly biased...)
Best
Rich Saitz
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