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Category: Informed Consent

Quality-Improvement Research and Informed Consent

  By admin Archives, Clinical Trials, Informed Consent

Franklin G. Miller, Ezekiel J. Emanuel | The New England Journal of Medicine | 21 Feb 2008 Tens of thousands of patients die each year because of hospitals’ failure to adhere consistently to standard procedures of safe and effective medical care.… Continue reading

Informed consent in Ghana: what do participants really understand?

  By admin Archives, Clinical Trials, Informed Consent

Hill Z., Tawiah-Agyemang C., Odei-Danso S., Kirkwood B. | Journal of Medical Ethics | 2008 | NCBI-PubMed ABSTRACT OBJECTIVES: To explore how subjects in a placebo-controlled vitamin A supplementation trial among Ghanaian women aged 15-45 years perceive the trial and… Continue reading

Interventions to improve research participant’s understanding in informed consent for research: A systematic review

  By admin Clinical Trials, Informed Consent

Flory, J., & Emanuel, E. | JAMA | 6 October 2004 | Vol. 292, No. 13 | Aim of article: To review research on interventions to improve research participants understanding of information disclosed in the informed consent process Read original… Continue reading

Seeking informed consent to cancer clinical trials: describing current practice

  By admin Archives, Clinical Trials, Informed Consent

Brown R. F., Butow P. N., Ellis P., Boyle F., Tattersall M. H. | Social Science and Medicine | June 2004 | NCBI-PubMed Abstract Clinical trials have come to be regarded as the gold standard for treatment evaluation. However, many… Continue reading

What makes clinical research in developing countries ethical? The benchmarks of ethical research

  By admin Archives, Clinical Trials, Informed Consent

Eamnuel E. J., Wendler D., Killen J., Grady C. | The Journal of Infectious Diseases | Vol. 189, Issue 5 | Oxford Journals | 1 March 2004 In recent years, there has been substantial debate about the ethics of research… Continue reading

Cancer clinical trial recruitment: The emerging role and perspectives of clinical research associates and data managers

  By admin Archives, Clinical Trials, Informed Consent

Martin Tattersall | Cancer | American Cancer Society | Volume 95, Issue 7, pages 1397–1400 | 1 October 2002 Clinical trials are an essential component of modern health care. The results of randomized clinical trials increasingly define current standards of care.… Continue reading

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  • Building Capacities and Leadership

    Our training and capacity-building initiatives are designed to strengthen women’s and young people’s (especially young women and girls) leadership in rural and peri-urban … Read more »

  • Research

    Over the last 25 years, Sama – Resource Group for Women and Health has conducted research on wide-ranging issues related to women’s health, public health, mental health, gender-based violence (GBV), and sexual and reproductive … Read more »

  • Advocacy

    With our strong and expanding connections at both the policy and grassroots levels, we are well placed to shape policy initiatives that reflect ground realities. We also create platforms that support community … Read more »

  • Knowledge Creation

    The knowledge resources we create cover a broad range of formats, including research papers, essays, articles, podcasts, training modules, policy briefs, information guides, videos, booklets, and posters … Read more »

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