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Det informerede samtykke i klinisk forskning kan forbedres

Forfatter(e)
Sarah Wadmann Det Nationale Institut for Kommuners og Regioners Analyse og Forskning, KORA Ugeskr Læger 2016;178:V03160192
Reference: 
Ugeskr Læger 2016;178:V03160192
Blad nummer: 
Sidetal: 
2-5
Clinical trial informed consent information for participants can be improved
Informed consent has been a legal right for patients participating in clinical research and an obligation for health professionals for a long time. A growing body of literature suggests that a considerable share of research participants do not read or understand the information they are given, or do not base their decisions on trial participation on the information. This article points out the challenges for health professionals arising from this situation and offers suggestions for how professionals can deal with the challenges.
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