False hopes and best data: consent to research and the therapeutic misconception.
about
Clinical trials and medical care: defining the therapeutic misconceptionThe law of incidental findings in human subjects research: establishing researchers' dutiesEthical issues in clinical trials involving nanomedicinePrioritizing Approaches to Engage Community Members and Build Trust in Biobanks: A Survey of Attitudes and Opinions of Adults within Outpatient Practices at the University of MarylandSharing the Knowledge: Sharing Aggregate Genomic Findings with Research Participants in Developing CountriesUnderstandings of genomic research in developing countries: a qualitative study of the views of MalariaGEN participants in Mali.Formative research on perceptions of biobanking: what community members thinkSeeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experienceQualitative thematic analysis of consent forms used in cancer genome sequencingPlanning for translational research in genomicsDoes random treatment assignment cause harm to research participants?Participants' perceptions and understanding of a malaria clinical trial in Bangladesh.Motivations for participating in a non-interventional gender-based violence survey in a low-income setting in South AfricaValid consent for genomic epidemiology in developing countriesAttitudes, understanding, and concerns regarding medical research amongst Egyptians: a qualitative pilot study.Tailoring consent to context: designing an appropriate consent process for a biomedical study in a low income setting.Informed consent from patients participating in medical education: a survey from a university hospital in Jamaica.Marginalized populations and drug addiction research: realism, mistrust, and misconceptionLong term understanding of study information in research participants with Parkinson's diseaseAccepting risk in clinical research: is the gene therapy field becoming too risk-averse?Integrating statistical and clinical research elements in intervention-related grant applications: summary from an NIMH workshop.Ethical issues in perinatal mental health researchReasons for participating in randomised controlled trials: conditional altruism and considerations for self.Utilizing Focus Groups with Potential Participants and Their Parents: An Approach to Inform Study Design in a Large Clinical TrialAmnestic MCI Patients' Perspectives toward Disclosure of Amyloid PET Results in a Research Context.An intervention to improve cancer patients' understanding of early-phase clinical trials.Payment of clinical research subjects.Informed consent in randomised controlled trials: development and preliminary evaluation of a measure of Participatory and Informed Consent (PIC).What research ethics should learn from genomics and society research: lessons from the ELSI Congress of 2011.Strengthening the informed consent process in international health research through community engagement: The KEMRI-Wellcome Trust Research Programme Experience.Ethical issues at the interface of clinical care and research practice in pediatric oncology: a narrative review of parents' and physicians' experiences.Repeated assessments of informed consent comprehension among HIV-infected participants of a three-year clinical trial in Botswana.The effect of early insulin therapy on pancreatic β-cell function and long-term glycemic control in newly diagnosed type 2 diabetic patientsUnrealistic optimism in early-phase oncology trials.Therapeutic misconception, misestimation, and optimism in participants enrolled in phase 1 trials.Rethinking the therapeutic misconception: social justice, patient advocacy, and cancer clinical trial recruitment in the US safety net.Informed consent and placebo effects: a content analysis of information leaflets to identify what clinical trial participants are told about placebosMotivations of patients with pulmonary arterial hypertension to participate in randomized clinical trialsPharmaceutical information systems and possible implementations of informed consent -- developing an heuristicPatients' perspectives and motivators to participate in clinical trials with novel therapies for rheumatoid arthritis
P2860
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P2860
False hopes and best data: consent to research and the therapeutic misconception.
description
1987 nî lūn-bûn
@nan
1987 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
False hopes and best data: consent to research and the therapeutic misconception.
@ast
False hopes and best data: consent to research and the therapeutic misconception.
@en
False hopes and best data: consent to research and the therapeutic misconception.
@nl
type
label
False hopes and best data: consent to research and the therapeutic misconception.
@ast
False hopes and best data: consent to research and the therapeutic misconception.
@en
False hopes and best data: consent to research and the therapeutic misconception.
@nl
prefLabel
False hopes and best data: consent to research and the therapeutic misconception.
@ast
False hopes and best data: consent to research and the therapeutic misconception.
@en
False hopes and best data: consent to research and the therapeutic misconception.
@nl
P2093
P1476
False hopes and best data: consent to research and the therapeutic misconception.
@en
P2093
P577
1987-04-01T00:00:00Z