Informed Consent Process
It is the policy of 澳门六合彩官网直播 that all research involving human subjects will be reviewed by the Institutional Review Board. The involvement of human subjects in research is not permitted until the IRB has reviewed and approved the research protocol. This means that no contact with subjects鈥攊ncluding recruitment and obtaining consent鈥攃an be initiated until the research has been approved, although researchers may contact organizations from which subjects will be recruited.
Furthermore, unless the consent process has been specifically waived by the IRB, no subjects may be included in research unless the investigator has obtained the legally effective informed consent of the subject or the subject鈥檚 legally authorized representative.
A consent document should have three parts: beginning, middle and end.
Beginning
- Who is doing the experiment.
- The nature, purpose and duration of the experiment, including the fact that the procedure is experimental.
- The uses to be made of the data.
Middle
- The methods to be employed.
- The hazards, inconveniences and risks the subjects will undergo, as far as they are known.
- The availability of compensation and treatment, if injured.
- The benefits that might be expected.
- Disclosure of alternate procedures the subject may choose if the experiment is therapeutically related.
- The conditions of participation, if any.
End
- A statement that the data are confidential and a description of the procedures to be employed in maintaining confidentiality.
- The fact that the subject is at liberty to withdraw his/her consent prior to the experiment, discontinue participation in the experiment at any time, or refuse to answer any questions, without prejudice.
- An offer to answer any questions as well as instructions as to how to contact the researcher, the IRB and the vice president for research, should questions arise later.
- A place for the date of signing and for the signature of the subject (and witness, is required).
Note: There can be no exculpatory language anywhere in the form.
Administering the consent document
- Pass out two forms鈥攐ne for subjects to sign and return to you and one for them to keep for their records.
- Read the form aloud as the subjects read it to themselves.
- After reading it aloud, summarize what is stated on the form.
- Allow time for questions.
- Schedule a break to allow subjects time to consider whether or not they want to participate.
FORMS
The information and sample documents in the compliance form section are provided to help researchers develop consent and assent documents customized to the design of the individual research project. If departmental letterhead is used, the header 鈥湴拿帕喜使偻辈モ and the department name may by omitted.
Additional resources
Contact
Julia Mays
(269) 387-8293
Associate Director of Compliance