IDEAS home Printed from https://ideas.repec.org/a/wly/nuhsci/v15y2013i1p3-8.html
   My bibliography  Save this article

Descriptive survey of Summer Genetics Institute nurse graduates in the USA

Author

Listed:
  • Kathleen T. Hickey
  • Robert R. Sciacca
  • Mary S. McCarthy

Abstract

The purpose of this study was to describe the clinical, research, educational, and professional activities that nurses are engaged in following participation in a 2 month intramural genetics training program. An online survey was administered in 2010 to graduates of the program sponsored by the US National Institute of Nursing Research from 2000 to 2009, in Bethesda, Maryland, USA. The electronic, voluntary survey was sent to 189 graduates via email. The survey included demographic characteristics, educational preparation, professional roles and responsibilities, and attitudes about genetic testing and privacy issues. Of the 95 graduates responding to the survey, 74% had doctorates and 70% were advanced practice nurses. All respondents reported incorporating genetics knowledge into daily clinical, academic, or research practices since completing the program, with 72% reporting being involved in genetically‐focused research (52% with research funding), 32% incorporating genetics into patient care, and 79% providing genetics education. Respondents working in a hospital setting or academic institution were more likely to desire additional training in genetics. National Institute of Nursing Research graduates have successfully integrated genomics into a variety of nursing practices.

Suggested Citation

  • Kathleen T. Hickey & Robert R. Sciacca & Mary S. McCarthy, 2013. "Descriptive survey of Summer Genetics Institute nurse graduates in the USA," Nursing & Health Sciences, John Wiley & Sons, vol. 15(1), pages 3-8, March.
    • Handle: RePEc:wly:nuhsci:v:15:y:2013:i:1:p:3-8
    DOI: 10.1111/j.1442-2018.2012.00693.x
    as

    Download full text from publisher

    File URL: https://doi.org/10.1111/j.1442-2018.2012.00693.x
    Download Restriction: no
    File URL: https://libkey.io/10.1111/j.1442-2018.2012.00693.x?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Francis S. Collins & Eric D. Green & Alan E. Guttmacher & Mark S. Guyer, 2003. "A vision for the future of genomics research," Nature, Nature, vol. 422(6934), pages 835-847, April.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. ZHU Chen & MOTOHASHI Kazuyuki, 2022. "Government R&D spending as a driving force of technology convergence," Discussion papers 22030, Research Institute of Economy, Trade and Industry (RIETI).
    2. Navon, Daniel & Shwed, Uri, 2012. "The chromosome 22q11.2 deletion: From the unification of biomedical fields to a new kind of genetic condition," Social Science & Medicine, Elsevier, vol. 75(9), pages 1633-1641.
    3. Sandra Millon Underwood & Aaron G. Buseh & Sheryl T. Kelber & Patricia E. Stevens & Leolia Townsend, 2013. "Enhancing the Participation of African Americans in Health-Related Genetic Research: Findings of a Collaborative Academic and Community-Based Research Study," Nursing Research and Practice, Hindawi, vol. 2013, pages 1-9, December.
    4. Sabatello, Maya & Insel, Beverly J. & Corbeil, Thomas & Link, Bruce G. & Appelbaum, Paul S., 2021. "The double helix at school: Behavioral genetics, disability, and precision education," Social Science & Medicine, Elsevier, vol. 278(C).
    5. Pinar, Candas & Almeling, Rene & Gadarian, Shana Kushner, 2018. "Does genetic risk for common adult diseases influence reproductive plans? Evidence from a national survey experiment in the United States," Social Science & Medicine, Elsevier, vol. 218(C), pages 62-68.
    6. Nchangwi Syntia Munung & Bongani M Mayosi & Jantina de Vries, 2017. "Equity in international health research collaborations in Africa: Perceptions and expectations of African researchers," PLOS ONE, Public Library of Science, vol. 12(10), pages 1-17, October.
    7. Gail E. Henderson, 2008. "Introducing Social and Ethical Perspectives on Gene—Environment Research," Sociological Methods & Research, , vol. 37(2), pages 251-276, November.
    8. Theresa M. Marteau & Scott Roberts & Susan LaRusse & Robert C. Green, 2005. "Predictive Genetic Testing for Alzheimer's Disease: Impact upon Risk Perception," Risk Analysis, John Wiley & Sons, vol. 25(2), pages 397-404, April.
    9. Timothy G Lesnick & Spiridon Papapetropoulos & Deborah C Mash & Jarlath Ffrench-Mullen & Lina Shehadeh & Mariza de Andrade & John R Henley & Walter A Rocca & J Eric Ahlskog & Demetrius M Maraganore, 2007. "A Genomic Pathway Approach to a Complex Disease: Axon Guidance and Parkinson Disease," PLOS Genetics, Public Library of Science, vol. 3(6), pages 1-12, June.
    10. Liang Yulan & Kelemen Arpad, 2016. "Bayesian state space models for dynamic genetic network construction across multiple tissues," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 15(4), pages 273-290, August.
    11. Cambrosio, Alberto & Keating, Peter & Schlich, Thomas & Weisz, George, 2006. "Regulatory objectivity and the generation and management of evidence in medicine," Social Science & Medicine, Elsevier, vol. 63(1), pages 189-199, July.
    12. Miller, Fiona Alice & Ahern, Catherine & Ogilvie, Jacqueline & Giacomini, Mita & Schwartz, Lisa, 2005. "Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification," Social Science & Medicine, Elsevier, vol. 61(12), pages 2536-2545, December.
    13. Marteau, Theresa M. & Weinman, John, 2006. "Self-regulation and the behavioural response to DNA risk information: A theoretical analysis and framework for future research," Social Science & Medicine, Elsevier, vol. 62(6), pages 1360-1368, March.
    14. O'Doherty, Kieran C. & Burgess, Michael M. & Edwards, Kelly & Gallagher, Richard P. & Hawkins, Alice K. & Kaye, Jane & McCaffrey, Veronica & Winickoff, David E., 2011. "From consent to institutions: Designing adaptive governance for genomic biobanks," Social Science & Medicine, Elsevier, vol. 73(3), pages 367-374, August.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:wly:nuhsci:v:15:y:2013:i:1:p:3-8. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Wiley Content Delivery (email available below). General contact details of provider: https://doi.org/10.1111/(ISSN)1442-2018 .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.