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I understand that my participation is voluntary and that I am free to withdraw at any time, without giving a reason and without cost. I understand that I will be given a copy of this consent form. I voluntarily agree to take part in this study.
Informed consent may not include language that: the research subject is made to ignore or appear to ignore any of the research subjects legal rights, releases or appears to release the investigator, the sponsor, the institution, or its agents from their liability for negligence.
I consent to participate in the research project and the following has been explained to me: the research may not be of direct benefit to me. my participation is completely voluntary. my right to withdraw from the study at any time without any implications to me.
A statement that the study involves research, an explanation of the purposes of the research and the expected duration of the subjects participation, a description of the procedures to be followed, and identification of any procedures which are experimental.
The following elements must be included in the Key Information section: The fact that consent is being sought for research and that participation is voluntary. The purposes of the research, expected duration of the prospective subjects participation, and procedures to be followed in the research.
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Most consent includes general risks, risks specific to the procedure, risks of no treatment and alternatives to treatment. Additionally, many consent forms express that there are no guarantees that the proposed procedure will provide a cure to the problem being addressed.
Hear this out loud PauseWrite directly to the reader, as though you are explaining the facts in person. Informed consent language should be written in the second person (you), not in the first person (I). Minimize passive voice to the extent possible.
Defining consent informed the person must be given all of the information about what the treatment involves, including the benefits and risks, whether there are reasonable alternative treatments, and what will happen if treatment does not go ahead.
The consent form must include: A statement that the study involves research. Purpose of the research. Procedures. Risks or discomforts to the subject. Benefits of the research to the subject. Treatment Alternatives. Costs of Participation. Confidentiality.
Hear this out loud PauseI have had the opportunity to ask questions about this research and I have received satisfactory answers. I understand the general purposes, risks and methods of this research. I consent to participate in the research project and the following has been explained to me: the research may not be of direct benefit to me.

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