If you are considering involvement in a research study, you should know that you have certain rights as a research participant.
You are likely to be presented with an informed consent form indicating approval by the IRB. This document is intended to provide you with relevant information necessary to decide whether or not you want to participate. This form itself should be coupled with a discussion of the research.
Generally, informed consent will involve a description of the following:
You should not sign the form agreeing to the research until all of your questions have been answered to your satisfaction. Signing this form does not waive any of your legal rights or alter your ability to stop participating at a later time. You should be given a copy of the form to take with you in case you have questions later.
Any participation in a research study is completely voluntary. You are free to decline to participate for any reason. You may also stop participating at any time or refuse to answer any individual questions. Even after you sign the consent form, you can stop. Should you decide to decline or stop participating, this decision will in no way influence any services to which you are otherwise entitled. For example, if you are a student, your teacher or professor can not hold this against you when determining your grade. If you are receiving treatment, that treatment can not be withheld if you do not agree to participate.
If at anytime during or after participating in a study you have any questions or concerns, you can contact either the researcher, using the contact information on the consent form, or one of the IRBs.
The Human Investigation Committees is responsible for oversight of biomedical research and can be reached at the firstname.lastname@example.org, (203) 785-4688.
The Human Subjects Committee oversees social and behavioral science research and can be reached at email@example.com, (203) 436-3650.
Whether or not you participate in a research study is entirely up to you.