Receiving a summary of the results of a trial: qualitative study of participants' views
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Mary Dixon-Woods | Sara Kenyon | C. Jackson | S. Kenyon | M. Dixon-Woods | Clare Jackson | Kate C Windridge | K. Windridge
[1] R Smith,et al. The rights of patients in research , 1995, BMJ.
[2] A. Strauss,et al. The discovery of grounded theory: strategies for qualitative research aldine de gruyter , 1968 .
[3] D. Elbourne,et al. Reactions of participants to the results of a randomised controlled trial: exploratory study , 1998, BMJ.
[4] Charles Weijer,et al. Informing study participants of research results: an ethical imperative. , 2003, IRB.
[5] S. Kenyon,et al. What do they know?: a content analysis of women's perceptions of trial information , 2004, BJOG : an international journal of obstetrics and gynaecology.
[6] Marc Taylor,et al. Research governance framework for health and social care. , 2002, Health & social care in the community.
[7] C. Weijer,et al. Considerations and costs of disclosing study findings to research participants , 2004, Canadian Medical Association Journal.
[8] M Gwinn,et al. Informed consent for population-based research involving genetics. , 2001, JAMA.
[9] E. Winer,et al. Offering participants results of a clinical trial: sharing results of a negative study , 2005, The Lancet.
[10] W. Tarnow-Mordi,et al. Broad-spectrum antibiotics for spontaneous preterm labour: the ORACLE II randomised trial , 2001, The Lancet.
[11] E. Winer,et al. Informing clinical trial participants about study results. , 2002, JAMA.
[12] C. Sklar,et al. Impact on survivors of retinoblastoma when informed of study results on risk of second cancers. , 2003, Medical and pediatric oncology.
[13] P. Pharoah,et al. Issues of consent and feedback in a genetic epidemiological study of women with breast cancer , 2003, Journal of medical ethics.
[14] J. López. How sociology can save bioethics . . . maybe. , 2004, Sociology of health & illness.
[15] S. Edwards,et al. Lay public's understanding of equipoise and randomisation in randomised controlled trials. , 2005, Health technology assessment.
[16] N. Pfeffer. Information and consent forms should use short words and sentences , 1996, BMJ.
[17] E. Winer,et al. Do patients participating in clinical trials want to know study results? , 2003, Journal of the National Cancer Institute.
[18] J. Kleijnen,et al. Reactions to treatment debriefing among the participants of a placebo controlled trial , 2005, BMC health services research.
[19] G. Elwyn,et al. Evolving the multiple roles of ‘patients’ in health‐care research: reflections after involvement in a trial of shared decision‐making , 2003, Health expectations : an international journal of public participation in health care and health policy.
[20] S. Kenyon,et al. Broad-spectrum antibiotics for preterm, prelabour rupture of fetal membranes: the ORACLE I randomised trial , 2001, The Lancet.
[21] Broad-spectrum antibiotics for preterm, prelabour rupture of fetal membranes: the ORACLE I randomised trial , 2001, The Lancet.
[22] V. Marzinotto,et al. DISSEMINATION TO RESEARCH SUBJECTS: OPERATIONALIZING INVESTIGATOR ACCOUNTABILITY , 2005, Accountability in research.
[23] M Dixon-Woods,et al. Writing wrongs? An analysis of published discourses about the use of patient information leaflets. , 2001, Social science & medicine.