Home Research PapersInformed are enroll or not to continue in the

Informed are enroll or not to continue in the

Informed consent is an authorization verbally or written
agreement to participate in research. Basically, participant involves are
voluntarily without compulsion and there are rational decision to participate.
There is a common procedure to go through before starting any study or
research. Informed consent document must be clearly written and must be
understandable by the participant. The consent must use the easy language and
should be define or explained in lay terms if the words are scientific or there
is medical terms. The informed consent is an important agreement before
register a participant.

Indeed, the informed consent is described an ethical codes
and legal for human subjects research. The aim of informed consent process is
to provide sufficient detailed information on the study. The participants are
entitled to ask question and researcher must answer those question.
Furthermore, allowing sufficient time for participant to make their decision.
Therefore, the participant will make decision whether they are enroll or not to
continue in the study. However, the participants have the right to refuse to
participate in this study without penalty if they wish.

We Will Write a Custom Essay Specifically
For You For Only $13.90/page!

order now

However, there are some issues relating research on human

1. Potential risk to subject

Potential risk can be widely categorized in human research.
Researcher need to take precaution to minimize potential of risk. The potential
risk in human research included;

a)            Risk of
physical includes injury, physical discomfort, illness or disease cause by
research method and procedure.

b)            Psychological
risks include the level of muscle tension such as depression, anxiety and loss
of self-esteem.

c)            Risks of
legal happened when the method of research violate the law rules designated. It
happen either by exposing the subject or other person engaging in an activity
where the subject can be a criminal.

d)            Social or
economic risk occur due to changes in the relationship between subjects and
others people who are disadvantage such as shame, loss of respect of others and
labeling the subject in a way that bring negative. While economically including
payment by subject to unnecessary procedures, loss of salary and any financial
costs such as damage to the subject’s marketability as a result of
participation in research.


2. Deceptive practice

Deceptive happen when a researcher gives false information
to the subject or deliberately misleads them about some of the key aspect of
research. This may include feedback on the subject involving creating false
beliefs about relationship or the manipulation of self-concept.

3.  Confidentially.

Confidentially needs to be maintained in order not to leak
information. The subjects have the right to be protected from injury or unauthorized
intrusions into their privacy and the preservation of their personal dignity.
Benefits of maintaining confidentially will help to establish trust between the
participant and researcher and participant feels more respected.


Research Ethics is essential to comply with ethical
principles and protect the rights and well-being of research participants.
Therefore, all research involving humans should be reviewed by ethical
committees to ensure that appropriate ethical standards are maintained.

The existing source of research ethics is the Belmont Report
published in 1979. It is a major work on ethics and healthcare research. Its
main purpose is to protect subjects and participants in clinical trials or
research studies. The Belmont Report was written by a panel of experts and
proposed three ethical research principles involving human subjects. The three
major ethical principles cited in Belmont are autonomy, beneficence, and

In general, autonomy can be defined as the right of an
individual to determine the activities they want or not to participate.
Specifically, autonomy requires an individual to understand what they are
asking to do, make a reasonable decision about the inclusion of their
impression on them, and make the choice to freely participate from the forces
of coercion.The principle of protecting autonomy is known as the consent
process, in which a researcher provides potential research participants with
complete disclosure of the types of research, risks, benefits and alternatives,
and gives a chance to ask before deciding to participate.The population is
considered as a reduced autonomy, based on the declining cognition such as
children, cognitive disabilities or the subject of mental illness. Other
conditions such as prisoners or people with severe illnesses are considered
vulnerable populations. In some cases, children and prisoners have specific
protection to protect their autonomy as required by regulations.

Beneficence can be substantially defined for the benefit of
research participants. The beneficence principle is behind research efforts to
minimize risk for participants and maximize benefits to participants and

Justice requires the careful selection of participants,
avoiding the population of imposed participants unfair to participate, such as
prisoners and organized children. The principle of justice requires that those
who carry out the burden of inquiry should benefit from the investigation, and
principles that are often violated by the export of clinical trials to less
developed countries.


I'm Alfred!

Would you like to get a custom essay? How about receiving a customized one?

Check it out