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Informed Consent

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Placebos      Clinical Trials      Patient Bill of Rights and Responsibilties      Informed Consent

        What is informed consent?

            One of the things that you will have to do before you can participate in a CPCRA research study
            is to give informed consent. This means that you will need to sign a piece of paper called a
            consent form that says that you agree to take part in the research study and that you know about
            different parts of the study including:
                The purpose and importance of the research
                The length of the study
                How often a doctor will check you
                How often a doctor will check you
                How often a doctor will check you
                Tests that you will have to take
                Costs of treatment
                How your records will be kept private
                Your treatment options
                All known side effects from the study drugs
                Information about who to call with questions

        Why do doctors have to obtain informed consent?

            The law requires doctors to tell patients who are going to be in a research study all about the
            study before they volunteer to participate in it. When you sign the consent form, you are saying
            that you have been told about all parts of the study, that you agree to all the conditions of the
            consent form. Your doctor will keep the consent form that you sign and will make a copy for you
            to keep.

        It's your decision!

            Your doctor will be careful about treating you with the study drug and will check you closely for
            any side effects, but it is still important for you to read the consent form very carefully of have
            someone else read it to you. Ask questions if you don't understand something. Even after you
            sign a consent form, taking part in a research study is your decision. A signed consent form will
            in no way bind you to continue the study and your health  care will not be affected. You should
            always, however, discuss this with your doctor. You will not give up any of your rights by signing
            a consent form.

            If you have any questions about informed consent, ask your doctor or nurse.