Taking to be a part of the research.

Taking
consent is not an easy process as we are getting someone permission by using
their data, knowledge and experience to use in a research and at the same time
we need to maintain the integrity of the information we have so it would have
not leaked out to other stranger that might use it for wrong purposes. The
process is vital in any form of research either is in written or verbal
informed consent. In the new world now days, almost everything we do require to
have informed consent. The purpose to ensure the participants well verse about
coming event that they are about to participate and confidentiality of their
information. In the other hand, it is also protecting the other company which
is the provider or researcher especially when there are medical issues being
raised.

When
it comes about taking the consent, the researcher should have explained in
detail of the objectives of the research. The researcher should inform the
future participants of all aspects of the research so that they are able to
influence the participants to willingly joining them in the research. The
participants must aware the risk or benefit from the research and they can ask
any enquiries regarding the research that they are going to. Any enquires
should be handle in full manner and professional way as to give a good
impression on how serious they are (researcher) to get the participant’s
attention to be a part of the research.

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            There
are a few issues that might disturb smoothness of the process taking the
consent. The common issue is language. Most of consent are written in English
version and there are in certain country, they will use their own national
language to write the consent. For those who would like to participate in the
research but unable to do so because they are not fully understanding the
concept and need extra hands to help them translating the consent form thus
it’s become time consuming. Some of if due to their unwillingness despite a
strong explanation has given to the respective participant. Another reason
could be that they are afraid of chances being misuses of their data by the
researcher.  If patient insist for not to
be part of the research, just let go and do not create any force on them.
Participants do have right to refuse in any sort of treatment if they wanted
too.

            When
we are taking the consent, it must ethically relevant. Patient’s priory comes
first, and their own values is something that we must respect. There are
certain principles has been discussed related to this topic. The ethical principles
emphasized more on beneficence and do no harm to them. So, as for that there
are five ethical principles should be considered when carrying out a research.

            The
principle number one is minimising the risk of harm to participants. The type
of harm can be subjective to such as physically, discomfort and distress or an
invasion to participant’s privacy and anonymity. There is no reason why
researcher wanted to put any harm to the participant’s, but it is something
that we could consider the risk of harm that we should try to be minimised.

            The
principle number two is obtaining informed consent which is the core of the
research. Explanation and details of research need to be inform and well
understand by the participants. Participants must be voluntarily, no force nor
being deceived to be involve in the research.

            Protecting
anonymity and confidentiality is the fourth principle of research ethics.  In research, these two components are important
as we should take care the information giving by the participants. Confidentiality
itself in research means that the data must be protected but how far we could
say and promise that data is being 100% protected and would not leak out? In research,
the step of processing the data will go through some level of analysis and this
could make the date been exposed to other people. Researcher must maintain the
promises of keeping the data right at the place and privacy is applied. By making
the participants anonymous, some how the researcher will unable to share the
outcome of the research that they have participate. Probably, they need to come
out some coding to identify the participant and at the same time no one able to
know about the participation.

 

 

           

            

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