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issue facing nurses’ researcher is the sources of funding for their
research.  Provate foundations and the federal
government provide much of the money for the nursing research projects.
However, many nurses researchers  are
turning to industry as another source of funding. According to Erlen (2000), cautioned
that ‘conflict of interest’ may occur when nurse researchers accept funds and
enter into financial relationships with industry

there might some misunderstanding that might occur. Besides that, some issue is
the participants may have a false expectation regarding the research. The participants might get involved in
research projects that they did not approve of due to misunderstandings or
misinterpretation concerning the experimental procedures (Escobedo et al.,
2007). The participant’s perception regarding the research might affect the
process of obtaining the informed consent because they afraid of the
consequences of the research on them. In this case, disclosing information to
them might scare them away.

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The process might create or result
several ethical issues if it is not being done properly. Misunderstandings
between the researchers and the participants will result due to communication
barriers such as language differences, religious dogma and believes. The
individual who signed the informed consent is assumed to have fully understand
the information that is stated in the consent form but it is difficult to
evaluate the level of understanding in the individual’s point of view. Nurse
researcher in clinical practice must take extra precautions to inform the
participants that they are acting in their capacity as researchers and not a
nurse instead. Potential participants may not be able to differentiate when the
nurse is acting as a caregiver or aa a researcher.

informed consent process is where the participant is informed regarding all
aspects of the trial, which are important for the participant to make a
decision and after studying all aspects of the trial, the participant
voluntarily confirms his or her willingness to participate in a particular
clinical trial and significance of the research for advancement of medical
knowledge and social welfare (Nijhawan et al., 2013)

Informed consent is a fundamental
ethical requirements for research with human subjects. It is when a subject voluntarily agrees to participate in a research
study in which he or she has full understanding of the study before the study
begins (Nieswiadomy, 2014).  A
subject voluntary agress to participate in a research study in which she/he has
full understanding of the study before the study begins. Informed consent
concern subjects’ participation in research in which they have full
understanding of the study before the study begins.

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