Literature DB >> 17844890

The oncology nurse's role in the informed consent process.

Virginia Chih-Yi Sun1, Tami Borneman.   

Abstract

Cancer clinical trials are a necessary component of the effort to improve cancer prevention, diagnosis, and treatment. Essential to this process is the informed consent of the individuals who participate in these research studies. The purpose of this article is to describe patient, provider, and informed consent process issues with presentations of data reported in the current literature. The role of nursing in the facilitation of informed consent is discussed.

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Year:  2007        PMID： 17844890

Source DB:  PubMed          Journal:  Oncology (Williston Park)        ISSN： 0890-9091            Impact factor:   2.990


  3 in total

1.  The Role of Oncology Nurses in Discussing Clinical Trials.

Authors:  Susan A Flocke; Elizabeth Antognoli; Barbara J Daly; Brigid Jackson; Sarah E Fulton; Tasnuva M Liu; Jessica Surdam; Sharon Manne; Neal J Meropol
Journal:  Oncol Nurs Forum       Date:  2017-09-01       Impact factor: 2.172

2.  A National Study of Oncology Nurses Discussing Cancer Clinical Trials With Patients.

Authors:  Susan A Flocke; Nora L Nock; Sarah Fulton; Seunghee Margevicius; Sharon Manne; Neal J Meropol; Barbara J Daly
Journal:  West J Nurs Res       Date:  2019-02-19       Impact factor: 1.967

Review 3.  Parents' Insights into Pediatric Oncology Phase I Clinical Trials: Experiences from Their Child's Participation.

Authors:  Stacey Crane; James M Croop; Jill Lee; Jamie Walski; Joan Haase
Journal:  Semin Oncol Nurs       Date:  2021-06-18       Impact factor: 3.527
  3 in total

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