Information Sheets and Informed Consent Forms for Clinical Study Participants: Towards Standardised Recommendations?
- 1 May 2009
- journal article
- review article
- Published by Elsevier BV
- Vol. 64 (3), 179-186
- https://doi.org/10.2515/therapie/2009035
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Improvement of the comprehension of written information given to healthy volunteers in biomedical research: a single-blind randomized controlled studyFundamental & Clinical Pharmacology, 2007
- Impact of French 'Comites de Protection des Personnes' on the readability of informed consent documents (ICD) in biomedical research: more information, but not better informationFundamental & Clinical Pharmacology, 2005
- Lisibilité de l’information écrite destinée aux sujets se prêtant à une recherche biomédicale: Une nécessaire remise en questionLa Presse Médicale, 2005
- Consent Documents for Oncology Trials: Does Anybody Read These Things?American Journal of Clinical Oncology, 2004
- Can We Ensure That All Research Subjects Give Valid Consent?Archives of Internal Medicine, 2004
- Interventions to Improve Research Participants' Understanding in Informed Consent for ResearchJAMA, 2004
- Modifying a Standard Industry Clinical Trial Consent Form Improves Patient Information Retention as Part of the Informed Consent ProcessAcademic Emergency Medicine, 2001
- Can the written information to research subjects be improved?--an empirical study.Journal of Medical Ethics, 1999