about
A review of approaches to improve participation of culturally and linguistically diverse populations in clinical trialsHuman Subjects Protection and Technology in Prevention Science: Selected Opportunities and ChallengesEthical Challenges and Lessons Learned During the Clinical Development of a Group A Meningococcal Conjugate VaccineCulturally and Linguistically Diverse Populations in Medical Research: Perceptions and Experiences of Older Italians, Their Families, Ethics Administrators and ResearchersVoluntary participation and comprehension of informed consent in a genetic epidemiological study of breast cancer in NigeriaProcedures of recruiting, obtaining informed consent, and compensating research participants in Qatar: findings from a qualitative investigationSexual, Reproductive Health Needs, and Rights of Young People in Slum Areas of Kampala, Uganda: A Cross Sectional Study.Politics, Culture, and Governance in the Development of Prior Informed Consent in Indigenous Communities.Applying research ethics guidelines: the view from a sub-saharan research ethics committee.Consenting of the vulnerable: the informed consent procedure in advanced cancer patients in Mexico.Ethical practices for health research in the Eastern Mediterranean region of the World Health Organization: a retrospective data analysisEthics Review Committee approval and informed consent: an analysis of biomedical publications originating from Sri LankaSecuring recruitment and obtaining informed consent in minority ethnic groups in the UK.Understanding and retention of the informed consent process among parents in rural northern Ghana.Understanding of research: a Sri Lankan perspectiveA mixed-methods study on perceptions towards use of Rapid Ethical Assessment to improve informed consent processes for health research in a low-income settingTailoring the process of informed consent in genetic and genomic researchInformed consent in otolaryngologic surgery: case scenario from a nigerian specialist hospital.Theoretical model of critical issues in informed consent in HIV vaccine trialsInformed consent and researchAssessing the quality of informed consent in a resource-limited setting: a cross-sectional study.Navigating the challenges of global reproductive health research.Challenges to obtaining parental permission for child participation in a school-based waterpipe tobacco smoking prevention intervention in Qatar.Lost in translation: assessing effectiveness of focus group questioning techniques to develop improved translation of terminology used in HIV prevention clinical trials.Participants' understanding of informed consent in clinical trials over three decades: systematic review and meta-analysis.Pharmacogenomic technologies: a necessary "luxury" for better global public health?Volunteer experiences and perceptions of the informed consent process: Lessons from two HIV clinical trials in Uganda.Adapting ethical guidelines for adolescent health research to street-connected children and youth in low- and middle-income countries: a case study from western KenyaConducting environmental health research in the Arabian Middle East: lessons learned and opportunities.Community Knowledge, Perceptions, and Practices Associated with Urogenital Schistosomiasis among School-Aged Children in Zanzibar, United Republic of Tanzania.A qualitative study using traditional community assemblies to investigate community perspectives on informed consent and research participation in western KenyaDiverse perceptions of the informed consent process: implications for the recruitment and participation of diverse communities in the National Children's Study.Understanding of research, genetics and genetic research in a rapid ethical assessment in north west Cameroon.Faith-based NGOs and healthcare in poor countries: a preliminary exploration of ethical issues.Exploring informed consent in HIV clinical trials: A case study in Uganda.Comprehensive Format of Informed Consent in Research and Practice: A Tool to uphold the Ethical and Moral StandardsUnderstanding of Essential Elements Required in Informed Consent Form among Researchers and Institutional Review Board MembersRecall and decay of consent information among parents of infants participating in a randomized controlled clinical trial using an audio-visual tool in The Gambia.Bioethics In Practice: Understanding Understood Consent.Informed consent for clinical treatment in low-income setting: evaluating the relationship between satisfying consent and extent of recall of consent information.
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description
im Oktober 2004 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 October 2004
@en
наукова стаття, опублікована в жовтні 2004
@uk
name
Beyond informed consent
@en
type
label
Beyond informed consent
@en
prefLabel
Beyond informed consent
@en
P1476
Beyond informed consent
@en
P2093
Zulfiqar A Bhutta
P304
P407
P577
2004-10-01T00:00:00Z