- ►critcaremed.com DJ Willison, C Emerson, KV Szala-Meneok, E … - British Medical Journal, 2008 - jme.bmj.com Introduction: Variation across research ethics boards (REBs) in conditions
placed on access to medical records for research purposes raises concerns around
negative impacts on research quality and on human subject protection, ... Cited by 10 - Related articles - BL Direct - All 4 versions
AL Dunlop, T Graham, Z Leroy, K Glanz, B … - Annals of Epidemiology, 2007 - Elsevier For a purposive sample of 384 African American outpatients at four metropolitan
primary care clinics from August 2005 through May 2006, willingness to
participate in a hypothetic clinical research study of an antihypertensive ... Cited by 7 - Related articles - All 6 versions
TJ Beebe, NJ Talley, M Camilleri, SM Jenkins, … - Medical Care, 2007 - journals.lww.com Timothy J. Beebe, PhD,* Nicholas J. Talley, MD, PhD,†‡ Michael Camilleri,
MD,† Sarah M. Jenkins, MS,* Kari J. Anderson, BS,* G. Richard Locke III,
MD,†‡ ... Background: There has been speculation that the Health ... Cited by 5 - Related articles - BL Direct - All 4 versions
- ►nih.gov DJ Willison, L Schwartz, J Abelson, C … - Journal of the American Medical Informatics …, 2007 - Elsevier Alternatives to Project-specific Consent for Access to Personal Information for
Health Research: What Is the Opinion of the Canadian Public? ... This study
sought to determine public opinion on alternatives to project-specific ... Cited by 4 - Related articles - All 7 versions
K El Emam, FK Dankar, R Issa, E Jonker, D … - Journal of the American Medical Informatics …, 2009 - Elsevier Explicit patient consent requirements in privacy laws can have a negative impact
on health research, leading to selection bias and reduced recruitment. Often
legislative requirements to obtain consent are waived if the information ... Cited by 3 - Related articles - All 4 versions
RJ Helmreich, V Hundley, A Norman, J … - NURSING FOR WOMENS HEALTH, 2007 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 1 - Related articles - BL Direct - All 3 versions
- ►critcaremed.com B Wilfond - The Journal of Trauma, 2007 - journals.lww.com The balance of potential benefits and risks to research participants is one of
the central ethical issues in evaluating biomedical research.1 Although this
balance is particu- larly salient in intervention studies because the ... Cited by 1 - Related articles - BL Direct - All 4 versions
H Länsimies-Antikainen, T Laitinen, R … - Scandinavian journal of caring sciences, 2009 - ncbi.nlm.nih.gov Objective: Informed consent is ethically and legally required for all biomedical
and health research involving human participants. This study analyses the
realization of informed consent in health research from the point of view ... Related articles
H Länsimies-Antikainen, AM Pietilä, V … - Gerontology, 2009 - content.karger.com Background: The informed consent process is the legal and ethical cornerstone of
health research and is essential to ensure that participants in health research
really understand the information they receive. Clinical studies often fail ...
HLA MNSc, T Laitinen, R Rauramaa, AMP … - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Related articles