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To ensure informed consent, a consent form must include the following: A statement of activity. The purpose of the activity. Procedures. Risks to the participant. Benefits to the participant. Cost of participation. Confidentiality. Voluntary participation.
Considerations in preparing the informed consent document: Elements of consent present. Complete explanations. Lay language. Protection of confidentiality. No unproven claims of effectiveness. Device studies include a statement that the study includes an evaluation of the safety of the test article.
If you prefer to write your own consent document, you may do so, but be sure to include all required elements of informed consent.
The consent form must identify the subjects alternatives to participation in the protocol and should offer a discussion of their relative advantages and disadvantages. It is usually not necessary to provide a full account of the risks and benefits of alternative treatments in the research consent form.
To achieve truly informed consent, four criteria have been identified: Information disclosure. Competence. Comprehension. Voluntariness.

People also ask

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.
A consent form is a document that someone signs to show that they will allow something to happen. Consent forms are used in psychology to insure that a person is aware of what they are agreeing to do and of any risks or costs that may exist.
Provide the title of the research project, the researcher(s) name, supervisors name (for 2. student research), the Unit in which the researcher is based and the name of the governing institution. State that the PIS has been read and the participant has had the opportunity to ask 3. questions of the researcher.

administration record consent form