Analyser av pasientinformasjon for kliniske studier
- Prosjektnummer
- 46013700
- Ansvarlig person
- Kari Sand
- Institusjon
- NTNU, IKM
- Prosjektkategori
- Phd-stipend 2006
- Helsekategori
- Cancer
- Forskningsaktivitet
- 8. Health Services
Readability of informed consent documents (1987-2007) for clinical trials: a linguistic analysis.
J Empir Res Hum Res Ethics 2012 Oct;7(4):67-78.
PMID: 23086049 - Inngår i doktorgradsavhandlingen
The length of consent documents in oncological trials is doubled in twenty years.
Ann Oncol 2009 Feb;20(2):379-85. Epub 2008 okt 15
PMID: 18922881
Lung cancer patients' perceptions of informed consent documents.
Patient Educ Couns 2008 Aug. Epub 2008 aug 6
PMID: 18691845
Readability of Informed Consent Documents (ICDs) in Clinical Trials (1987-2007) - A Linguistic Approach
The 7th World Research Congress of the European Association for Palliative Care (EAPC) 2012
Blir informert samtykke forstått?
Tidsskr Nor Legeforen 2011; 131:1175
The Understanding of Informed Consent Information—Definitions and Measurements in Empirical Studies
AJOB Primary Research Volume 1, Issue 2 April 2010 , pages 4 - 24
The Understanding of Informed Consent Information—Definitions and Measurements in Empirical Studies
6th Research Congress of the EAPC, Glasgow UK, 10-12th June 2010
The understanding of informed consent information – definitions and measurements in empirical studies.
4th International Trondheim Conference on palliative care
The understanding of informed consent information - definitions and measurements in empirical studies
2008 International Conference On Communication In Healthcare
Consent documents for a palliative chemotherapy trial – what do the patients actually perceive?
5th Research Forum of the European Association for Palliative Care
Informed consent documents for cancer research - textual and contextual factors of relevance for understanding
- Disputert:
- november 2012
- Hovedveileder:
- Jon Håvard Loge
eRapport er utarbeidet av Sølvi Lerfald og Reidar Thorstensen, Regionalt kompetansesenter for klinisk forskning, Helse Vest RHF, og videreutvikles av de fire RHF-ene i fellesskap, med støtte fra Helse Vest IKT
Alle henvendelser rettes til Helse Midt-Norge RHF - Samarbeidsorganet og FFU