Parental perceptions of the informed consent process in pediatric oncology clinical trials
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چکیده
منابع مشابه
The oncology nurse's role in the informed consent process.
Cancer clinical trials are a necessary component of the effort to improve cancer prevention, diagnosis, and treatment. Essential to this process is the informed consent of the individuals who participate in these research studies. The purpose of this article is to describe patient, provider, and informed consent process issues with presentations of data reported in the current literature. The r...
متن کاملInformed consent, parental permission, and assent in pediatric practice.
The statement on informed consent, parental permission, and patient assent has a long and extraordinary history. The first draft of this document, prepared by William G. Bartholome, MD, was presented to the original American Academy of Pediatrics (AAP) Committee on Bioethics in 1985. Bill put his soul into the manuscript and has watched over it carefully ever since. Now, a decade later, those w...
متن کاملInformed consent for clinical trials: a review.
OBJECTIVE To identify and highlight challenges related to informed consent process for clinical trials in sub-Saharan Africa. DATA SOURCES Published original research findings and reviews in the English literature, together with anecdotal information from our current professional experiences with clinical trials. DESIGN Review of peer-reviewed articles. DATA EXTRACTION Online searches wer...
متن کاملInformed Consent: A Clinical Trials Perspective.
The primary goal of the thousands of registered trials in cancer research is to extend survival. With evaluation of efficacy, safety, and tolerability, healthcare providers must ensure that the principles described in the Belmont Report are upheld and that patients are truly informed when signing a consent form. In this article, two cases are highlighted, and reasons for participating in clinic...
متن کاملVolunteer experiences and perceptions of the informed consent process: Lessons from two HIV clinical trials in Uganda.
BACKGROUND Informed consent as stipulated in regulatory human research guidelines requires that a volunteer is well-informed about what will happen to them in a trial. However researchers are faced with a challenge of how to ensure that a volunteer agreeing to take part in a clinical trial is truly informed. We conducted a qualitative study among volunteers taking part in two HIV clinical trial...
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ژورنال
عنوان ژورنال: Journal of Nursing Education and Practice
سال: 2013
ISSN: 1925-4059,1925-4040
DOI: 10.5430/jnep.v3n11p71