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Journal Abstract Search

187 related items for PubMed ID: 22104045

  • 1. Designing research with hospice and palliative care populations.
    Wohleber AM, McKitrick DS, Davis SE.
    Am J Hosp Palliat Care; 2012 Aug; 29(5):335-45. PubMed ID: 22104045
    [Abstract] [Full Text] [Related]

  • 2. Informed consent in palliative care clinical trials: challenging but possible.
    Agar M, Ko DN, Sheehan C, Chapman M, Currow DC.
    J Palliat Med; 2013 May; 16(5):485-91. PubMed ID: 23631612
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  • 4. Refining a checklist for reporting patient populations and service characteristics in hospice and palliative care research.
    Currow DC, Tieman JJ, Greene A, Zafar SY, Wheeler JL, Abernethy AP.
    J Pain Symptom Manage; 2012 May; 43(5):902-10. PubMed ID: 22445274
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  • 5. A concept analysis of palliative care in the United States.
    Meghani SH.
    J Adv Nurs; 2004 Apr; 46(2):152-61. PubMed ID: 15056328
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  • 8. Ethical issues of recruitment and enrollment of critically ill and injured patients for research.
    Richmond TS, Ulrich C.
    AACN Adv Crit Care; 2007 Apr; 18(4):352-5. PubMed ID: 17978608
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  • 10. Reconciling informed consent and 'do no harm': ethical challenges in palliative-care research and practice in chronic obstructive pulmonary disease.
    Gardiner C, Barnes S, Small N, Gott M, Payne S, Seamark D, Halpin D.
    Palliat Med; 2010 Jul; 24(5):469-72. PubMed ID: 20444768
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  • 11. Review: a narrative review of the published ethical debates in palliative care research and an assessment of their adequacy to inform research governance.
    Duke S, Bennett H.
    Palliat Med; 2010 Mar; 24(2):111-26. PubMed ID: 19965950
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  • 12. Research versus innovation: real differences.
    Morreim H.
    Am J Bioeth; 2005 Mar; 5(1):42-3; author reply W15-8. PubMed ID: 16036658
    [No Abstract] [Full Text] [Related]

  • 13. Knowledge and attitudes of terminally ill patients and their family to palliative care and hospice services in Nigeria.
    Adenipekun A, Onibokun A, Elumelu TN, Soyannwo OA.
    Niger J Clin Pract; 2005 Jun; 8(1):19-22. PubMed ID: 16392451
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  • 14. Stakeholder perspectives on ethical challenges in HIV vaccine trials in South Africa.
    Essack Z, Koen J, Barsdorf N, Slack C, Quayle M, Milford C, Lindegger G, Ranchod C, Mukuka R.
    Dev World Bioeth; 2010 Apr; 10(1):11-21. PubMed ID: 19459900
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  • 15. Literature review: considerations in undertaking focus group research with culturally and linguistically diverse groups.
    Halcomb EJ, Gholizadeh L, DiGiacomo M, Phillips J, Davidson PM.
    J Clin Nurs; 2007 Jun; 16(6):1000-11. PubMed ID: 17518876
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  • 16. Voluntary informed consent in research and clinical care: an update.
    Cahana A, Hurst SA.
    Pain Pract; 2008 Jun; 8(6):446-51. PubMed ID: 19000172
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  • 17. Improving subject recruitment by maintaining truly informed consent: a practical benefit of disclosing adverse clinical trial results.
    Shah KR, Batzer FR.
    Am J Bioeth; 2009 Aug; 9(8):36-7. PubMed ID: 19998157
    [No Abstract] [Full Text] [Related]

  • 18. Topics in research: structuring studies in palliative care.
    Davis MP, Mitchell GK.
    Curr Opin Support Palliat Care; 2012 Dec; 6(4):483-9. PubMed ID: 23123820
    [Abstract] [Full Text] [Related]

  • 19. Designing and conducting randomized controlled trials in palliative care: A summary of discussions from the 2010 clinical research forum of the Australian Palliative Care Clinical Studies Collaborative.
    Shelby-James TM, Hardy J, Agar M, Yates P, Mitchell G, Sanderson C, Luckett T, Abernethy AP, Currow DC.
    Palliat Med; 2012 Dec; 26(8):1042-7. PubMed ID: 21844138
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  • 20. Research methodologies in palliative care: a bibliometric analysis.
    Payne SA, Turner JM.
    Palliat Med; 2008 Jun; 22(4):336-42. PubMed ID: 18541637
    [Abstract] [Full Text] [Related]

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