Journal article
Ethical communication in clinical trials
Abstract
BACKGROUND: Informed consent has been proposed as the optimal method for ensuring the ethical entry of patients into clinical trials. However, it is known that problems with informed consent exist from the perspective of both patients and physicians. This has led to the suggestion that a third party, such as a research nurse or data manager, should be responsible for obtaining informed consent. The objective of this study was to explore the …
Authors
Loh WY; Butow PN; Brown RF; Boyle F
Journal
Cancer, Vol. 95, No. 11, pp. 2414–2421
Publisher
Wiley
Publication Date
December 2002
DOI
10.1002/cncr.10994
ISSN
1097-0142
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AdultClinical Trials as TopicCommunicationDecision MakingEthics, MedicalFemaleFocus GroupsHealth PersonnelHospitals, TeachingHumansInformation ManagementInformed ConsentInterprofessional RelationsKnowledgeMaleMiddle AgedNeoplasmsPhysician-Patient RelationsWorkforceAdenocarcinomaAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Squamous CellCisplatinDeoxycytidineHematologic DiseasesNasopharyngeal NeoplasmsNeoplasm Recurrence, LocalSurvival RateTreatment OutcomeGemcitabine