7/26/2023 0 Comments Informed consent form![]() Whether the results can be used for research purposes. What the test results mean, including positive and negative results, and the potential for uninformative results or incorrect results such as false positives or false negatives.Īny physical or emotional risks associated with the test. How the test will be carried out (for example, a blood sample). Several factors are commonly included on an informed consent form:Ī general description of the test, including the purpose of the test and the condition for which the testing is being performed. If the person wishes to have the test, he or she will then usually read and sign a consent form. The health care provider will discuss the test and answer any questions. Informed consent for genetic testing is generally obtained by a doctor or genetic counselor during an office visit. For children and others who are unable to make their own medical decisions (such as people with impaired mental status), informed consent can be given by a parent, guardian, or other person legally responsible for making decisions on that person's behalf. In general, informed consent can only be given by adults who are competent to make medical decisions for themselves. "Informed" means that the person has enough information to make an educated decision about testing "consent" refers to a person's voluntary agreement to have the test done. The process of educating a person about the test and obtaining permission to carry out testing is called informed consent. Before a person has a genetic test, it is important to fully understand the testing procedure, the benefits and limitations of the test, and the possible consequences of the test results.
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