Recruiting Terminally Ill Patients into Non-Therapeutic Oncology Studies: views of Health Professionals

[1]  Y. Khaliq,et al.  Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans , 2012 .

[2]  Y. Bombard,et al.  Genetic discrimination: international perspectives. , 2012, Annual review of genomics and human genetics.

[3]  Alicia M Ward,et al.  Cancer Management and Research Dovepress Deciding What Information Is Necessary: Do Patients with Advanced Cancer Want to Know All the Details? , 2022 .

[4]  Juri G. Gelovani,et al.  Methodological and practical challenges for personalized cancer therapies , 2011, Nature Reviews Clinical Oncology.

[5]  M. Kottow Ethical quandaries posing as conflicts of interest , 2010, Journal of Medical Ethics.

[6]  J. Tulsky,et al.  Can metaphors and analogies improve communication with seriously ill patients? , 2010, Journal of palliative medicine.

[7]  C. Reynaert,et al.  Les enjeux de la communication médecin-patient et l’importance des caractéristiques psychologiques du médecin , 2009 .

[8]  K. Rameshkumar Ethics in medical curriculum; Ethics by the teachers for students and society , 2009, Indian journal of urology : IJU : journal of the Urological Society of India.

[9]  E. Emanuel,et al.  The obligation to participate in biomedical research. , 2009, JAMA.

[10]  Amy P Abernethy,et al.  Oncologist communication about emotion during visits with patients with advanced cancer. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[11]  A. Abernethy,et al.  Studying communication in oncologist-patient encounters: The SCOPE Trial , 2006, Palliative medicine.

[12]  L. Knapp,et al.  A review of international and UK-based ethical guidelines for researchers conducting nontherapeutic genetic studies in developing countries , 2006, European Journal of Human Genetics.

[13]  E. Thomson,et al.  Concerns in a primary care population about genetic discrimination by insurers , 2005, Genetics in Medicine.

[14]  D. Razavi,et al.  Physicians' communication with a cancer patient and a relative: a randomized study assessing the efficacy of consolidation workshops. , 2005, Cancer.

[15]  L. McKee,et al.  Family Communication about Genetic Risk: The Little That Is Known , 2004, Public Health Genomics.

[16]  J. Weitzel,et al.  Genetic discrimination: the clinician perspective , 2004, Clinical genetics.

[17]  L. McKee,et al.  To tell or not to tell: barriers and facilitators in family communication about genetic risk , 2003, Clinical genetics.

[18]  A. Jubb Palliative care research: trading ethics for an evidence base , 2002, Journal of medical ethics.

[19]  A. Whelan Genetics in the Clinic: Clinical, Ethical, and Social Implications for Primary Care , 2001, Annals of Internal Medicine.

[20]  J. Karlawish,et al.  Are special ethical guidelines needed for palliative care research? , 2000, Journal of pain and symptom management.

[21]  K. McPherson,et al.  Cancer patients' information needs and information seeking behaviour: in depth interview study , 2000, BMJ : British Medical Journal.

[22]  K. Lloyd,et al.  Psychological distress among cancer patients and informed consent. , 1999, Journal of psychosomatic research.

[23]  D. Dudgeon,et al.  Ethical issues in palliative care research revisited , 1995, Palliative medicine.

[24]  J. de Haes,et al.  Doctor-patient communication: a review of the literature. , 1995, Social science & medicine.

[25]  J. L. Nelson Taking families seriously. , 1992, The Hastings Center report.

[26]  B. Raudonis Ethical Considerations in Qualitative Research with Hospice Patients , 1992, Qualitative health research.

[27]  M. Patton Qualitative research and evaluation methods , 1980 .

[28]  F. G.,et al.  The Family , 1906, Nature.