Research is required to improve theconditions.
Prepared for any research islikely to help society directly or indirectly. Before beginning collecting thedata, the researchers need to inform and obtain consent first to theparticipants.The meaning of informedconsent is an essential part of the researchers to get to the participantsbefore doing the research. Informed consent implies that participants are aware of the type of information you wantfrom them, why the information is being sought, what the purpose it will beingcarried out, how they are expected to participate in the study and how itdirectly effect to the.
It is important things to get consent voluntary andwithout any pressure to the participants.Information elements of the consents areparticipants must be fully noted. Subject should be confidential and anonymous.The informed consent form must be written in lay language to make participantseasy to understand about the research. The researcher must give time to answerquestions at any time the participants available.
The elements in the consent must bevoluntary without any pressure. Participants also must be free to withdrawconsent at any time they want. The consent form must contains explanation the aim of the research project, the ways howthe study will being conducted study, the harm and risk, the value and thebeneficial, privately, refusal from the study, harsh statement, consentform ,and the last thing must being sign by participants. A humansubject is defined as a living person about who will investigatorconducting research get the information. This includes studying of humans through observations orinterviews, psychological, physiological or medical testing or treatment,access to their personal document or other materials such as the collection anduse of their body organs, tissues or fluids.
Access to their details is personallyidentifiable confidential information form as a part of an existing publishedsource or database.An issues relating to this is the risk ofthe research to the participants. A risk can cause harm to participants,discomfort or inconvenience. The list of harm include physical harm such asinjury, illness and pain. Psychological harm which is feelings ofworthlessness, distress, guilt, anger or fear. For example, to expose of somethingsensitive or embarrassing information, or learning about the geneticpossibility of developing an untreatable disease. Another issues is to sought the sensitiveinformation.
In seeking this matter, it will make the participants may upset orembarrass to participate, but if we not ask for it, there is no way to soughtthis problem. For most people in this world, the sexual behaviour , drug use,marital status, salary, age are privacy and personal lifestyle without anyoneshould know about that things. So, incollecting the data about the sensitive information, the researchers need toexplain carefully and smoothly to the participants.
Keep the information privatelyand give them enough time without any pressure.Another issue is to keep all theinformation privately. Do not share theinformation we get from the participants with another besides the purpose ofthe study. It is unethical when we do so, so be careful. Make sure all confidentialityis maintained. Providing some present also one of theissue in research human subjects.
Some of the researchers provide some presentto their participants as appreciation because of their time involving in thestudy but some thinking is inducements. It depends to any researchers andparticipants about the present. The major ethical principles that guideresearchers in their works, respect the persons as human dignity, beneficence,and justice.Respect for persons. The principle of respectfor human as an individual involves acknowledge the existence of human beinghas value for themselves. Researchers must equally regard the value of those areinvolving in research.
The moral and ethical requirement is based on theacceptance of the participant’s autonomy. It is the important things and the responsibilityof the researcher to get informed consent from the participants and to maintainprivately on their behalf. From the beginning till the end of the researchprocess to the capacity of human beings to make their own decision without anypressure from anybody. When the participants are unable to make their owndecisions or have lack of ability to do so, respect for them by empowering themwhen possible, give them time and providing for their protection as necessary.Researchers should respect the privacy, confidentiality and cultural norms sensitivitiesof participants and what the relevant things, of their communities.
Anyspecific agreement made with the participants or the community should beaccomplished.The principle of beneficence is between thepotential benefit and risk for participation. The likely benefit of theresearch must justify any risks of harm or discomfort to participants or thewider community. Researchers must have to maximize possible benefits andminimize possible harm. Researchers are responsible for designing the researchto minimize the risks of harm or discomfort to participants, clarifying toparticipants the potential benefits and risk, and the welfare of theparticipants in the research.
Where there is no likely benefit to participants,the risk to participants should be lower than would be ethically acceptablewhere there are such likely benefits over there.The principle of justice involves regard forhuman similarity that each person share with others, that means should treatequally. It means a fair distribution of the burdens and benefits of researchand encompasses fair treatment in recruitment of participants and in the reviewof research. Researchers must ensure that the vulnerable are not exploited andthat eligible candidates who may benefit from participation are not excludedwithout good cause.