Open AccessISSN: 2167-1168
Journal of Nursing & Care
Book Reviews
Volume 11:3, 2022
*Address for Correspondence: Dilshada Rashid, Department of Pediatric
Surgery, SKIMS, Srinagar, Kashmir, India, E-mail: [email protected]
Copyright: © 2022 Rashid D. This is an open-access article distributed under the
terms of the Creative Commons Attribution License, which permits unrestricted
use, distribution, and reproduction in any medium, provided the original author
and source are credited.
Received: 05 March, 2022, Manuscript No. jnc-21-53252; Editor assigned: 08
March, 2022, PreQC No. P-53252; Reviewed: 19 March, 2022, QC No. Q-53252;
Revised: 20 March, 2022, Manuscript No. R-53252; Published: 27 March, 2022,
DOI: 10.37421/2167-1168.2022.11.520
Ethics in Nursing Research
Dilshada Rashid*
Department of Pediatric Surgery, SKIMS, Srinagar, Kashmir, India
Introduction
The Ethics are the moral principles that govern a person’s behaviour.
Research ethics may be referred to as doing what is mostly and legally right
in research. They are actually norms for conduct that distinguish between
right and wrong, and acceptable & unacceptable behaviour. Knowingly that
research is “a process of investigation leading to new insights, effectively
shared.” Research is a multi-stage process. Ethics are central to this process.
Researcher need to take care of various ethical issues at different levels of this
process [1-4].
Definition: Ethics in nursing research can be defined as the act of
moral principles which the researcher has to follow while conducting nursing
research to ensure the rights and welfare of individuals, groups or community
under study.
Importance of Ethics in Nursing Re-
search
Ethics within healthcare are important because workers must recognize
healthcare dilemmas, make good judgments and decision based on their
values while keeping within the laws that govern them. The important reasons
to support importance of ethics in nursing research are:
Protect the vulnerable group & other study participants from harmful
effects of the experimental intervention.
Participants are safeguarded from exploitation by researchers.
Establish risk-benefit ratio for the study subjects.
Ensure the fullest respect, dignity, privacy, disclosure of information &
fair treatment for study subjects.
Build the capability of subjects to accept or reject participation in study
and to have access to informed or written consent for participation in
research study.
Ethical Principles
The three broad principles on which standards of ethical conduct in
research are based: Beneficence, Respect for human dignity and Justice.
Principle of beneficence
Beneficence imposes a duty on researchers to minimize harm and
maximize benefits. Human research should be intended to produce benefits
for participants or a situation that is more common for others. Participants must
be provided with maximum physical, psychological, social & religious comfort
and undue disturbance and time utilization of the subjects should be avoided.
Participants must be assured that their information will not be used against
them in any way e,g person reporting drug abuse should not be exposed to the
of criminal authorities. Research must be conducted by scientifically qualified
expert. This principle covers multiple dimensions:
Freedom from Harm
Freedom from Exploitation
Benefits from Research
The Risk Benefit Ratio if the perceived risks to participants outweigh
the anticipated benefits of the research, the research should be either
abandoned or redesigned.
Principle of respect of human dignity
This principle includes the right to self-determination and right to full
disclosure. This principle of the ethics emphasizes on the freedom of choice,
where participants have right to accept or reject to be a part of the research
study. In addition, volunteers must be provided full information about the
research study and an informed consent must be obtained, preferably a written
one. The researcher under this principle must ensure following:
Participants have full right to question the researcher for any additional
information or clarification of doubts.
Participants have right to quit from the study at any stage of the
research study.
A fully informed consent must be taken from the participants. In case
of foetus, child, psychological, neurological, physical inability to give
informed consent; this can be obtained from parent or legal guardians.
The contents of an informed consent must include the
following:
Purpose of the research study, Procedural process & any intervention
involved in the study, expected time & nature of participant’s involvement in
the study, type of data /information to be obtained for respondents, details
of the support available in case any harm occurs to participants, details of
the potential discomfort or risk for participants in the study, description of the
expected benefits of the research study, there are certain ethical dilemmas
where taking consent may distort the actual situation & research finding.
Example: A study on nurses’ time utilization in productive & non-productive
activities during working period , Behaviour of the nurses with patients and
their family in surgical wards, Performance observation of the nurses in
medical ward.
Such ethical dilemmas must be dealt carefully, where informed consent
may be avoided until research does not actually harm the participants or
breach their privacy & take permission from competent authority. However,
strictly speaking, the ethical principles never permit this.
Principle of Justice
This principle concerns justice, which includes participants’ right to fair
treatment and their right to privacy.
The fair & non-discriminatory selection of the participant such as any
risk & benefits will be equally shared by study participants.
J Nurs Care, Volume 11:3, 2022Rashid D
Page 2 of 2
The fair treatment principle covers issues other than participant
selection. the right to fair treatment means that researchers must
treat people who decline to participate (or who with draw from
after initial agreement)in a non-prejudicial manner ,that they must
honour all agreements made with participants (including payment if
promised),that they demonstrate respect for the beliefs, habits & life
styles of people from different background or cultures.
Anonymity of participants & confidentiality of information must be
maintained.
No information collected from study participants can be used for other
than research purpose.
The vulnerable subjects such as children, pregnant women, mentally
ill, institutionalized (prisoners) people etc., who are easily accessible
must be protected from overuse & undue use for research purpose.
Obtain identifying information (e.g. name, address) from participants
only when it is essential to do so. Destroy identifying information as
quickly as is feasible.
References
1. Polit, Denise F., and Cheryl Tatano Beck. “Nursing research: Principles and
methods.” Lippincott Williams & Wilkins (2004).
2. Sharma, Suresh. “Nursing research and statistics.” Elsevier Health Sci (2018).
3. Polit, Denise F., and Cheryl Tatano Beck. “Nursing research: Generating and
assessing evidence for nursing practice.” Lippincott Williams & Wilkins (2008).
4. Showkat, Nayeem, and Huma Parveen. "In-depth interview." Quadrant-I (e-Text)
(2017).
How to cite this article: Rashid, Dilshada. “Ethics in Nursing Research.” J Nurs
Care 11 (2022): 520.