Comprehension during informed consent in a less-developed country.
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Extended discussion of information for informed consent for participation in clinical trialsOptimizing the HIV/AIDS informed consent process in IndiaAspects of vulnerable patients and informed consent in clinical trialsConsent and community engagement in diverse research contextsDigitised audio questionnaire for assessment of informed consent comprehension in a low-literacy African research population: development and psychometric evaluationRecruiting for epigenetic research: facilitating the informed consent processApplying research ethics guidelines: the view from a sub-saharan research ethics committee.Seeking consent for research with indigenous communities: a systematic reviewValid consent for genomic epidemiology in developing countriesEnrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa.Understanding and retention of the informed consent process among parents in rural northern Ghana.Formative Evaluation of Participant Experience With Mobile eConsent in the App-Mediated Parkinson mPower Study: A Mixed Methods Study.Comparison of group counseling with individual counseling in the comprehension of informed consent: a randomized controlled trialAre women who work in bars, guesthouses and similar facilities a suitable study population for vaginal microbicide trials in Africa?How informed is consent in vulnerable populations? Experience using a continuous consent process during the MDP301 vaginal microbicide trial in Mwanza, Tanzania.Repeated assessments of informed consent comprehension among HIV-infected participants of a three-year clinical trial in Botswana.Comparison of closed-ended, open-ended, and perceived informed consent comprehension measures for a mock HIV prevention trial among women in Tanzania.A randomized trial of enhanced HIV risk-reduction and vaccine trial education interventions among HIV-negative, high-risk women who use noninjection drugs: the UNITY studyInformed consent in international research: the rationale for different approaches.Continuing review of ethics in clinical trials: a surveillance study in Iran.Motivations, understanding, and voluntariness in international randomized trials.Experiencing everyday ethics in context: frontline data collectors perspectives and practices of bioethicsCould the decision of trial participation precede the informed consent process? Evidence from Burkina Faso.An Ad5-vectored HIV-1 vaccine elicits cell-mediated immunity but does not affect disease progression in HIV-1-infected male subjects: results from a randomized placebo-controlled trial (the Step study)Using formative research to develop a context-specific approach to informed consent for clinical trials.Informed consent and participant perceptions of influenza vaccine trials in South AfricaThe effect of HIV and HPV coinfection on cervical COX-2 expression and systemic prostaglandin E2 levelsResearch in family medicine in developing countriesIncorporating a quiz into informed consent processes: qualitative study of participants' reactions.Descriptive ethics: a qualitative study of local research ethics committees in Mexico.A qualitative study using traditional community assemblies to investigate community perspectives on informed consent and research participation in western KenyaImproved participants' understanding in a healthy volunteer study using the SIDCER informed consent form: a randomized-controlled study.Introduction: the Fogarty International Research Ethics Education and Curriculum Development Program in historical contextObtaining informed consent from HIV-infected pregnant women, Abidjan, Côte d'Ivoire.Early versus standard antiretroviral therapy for HIV-infected adults in Haiti.Cohort Profile: Caribbean, Central and South America Network for HIV research (CCASAnet) collaboration within the International Epidemiologic Databases to Evaluate AIDS (IeDEA) programme.Informing the uninformed: optimizing the consent message using a fractional factorial designComposition, training needs and independence of ethics review committees across Africa: are the gate-keepers rising to the emerging challenges?Assessing whether consent for a clinical trial is voluntaryManaging Ethical Challenges to Mental Health Research in Post-Conflict Settings.
P2860
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P2860
Comprehension during informed consent in a less-developed country.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Comprehension during informed consent in a less-developed country.
@en
Comprehension during informed consent in a less-developed country.
@nl
type
label
Comprehension during informed consent in a less-developed country.
@en
Comprehension during informed consent in a less-developed country.
@nl
prefLabel
Comprehension during informed consent in a less-developed country.
@en
Comprehension during informed consent in a less-developed country.
@nl
P50
P1433
P1476
Comprehension during informed consent in a less-developed country.
@en
P2093
Cécile Marotte
Warren D Johnson
P304
P356
10.1016/S0140-6736(02)11338-9
P407
P577
2002-10-01T00:00:00Z