Informed Consent

Informed consent is a legal and ethical term defined as the consent by a client to a proposed medical or psychotherapeutic procedure, or for participation in a research project or clinical study. In order for the consent to be informed, the client must first achieve a clear understanding of the relevant facts, risks and benefits, and available alternatives involved. Informed consent requires legal documentation in all 50 states. The concept of informed consent originated with the recognition that individuals have rights: to freedom, autonomy, and human dignity. Informed consent as a professional practice is a legal procedure to ensure that patients, clients, and research participants are aware of all the potential risks and costs involved in a treatment or procedure. The elements of informed consent include informing the client of the nature of the treatment, possible alternative treatments, and the potential risks and benefits of the treatment.

Keeping these ideas in mind, please respond to questions # 2, 3 and 4 on Page 186 of the course textbook in your initial discussion post.

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2. Does a client have a right to be ignorant of the risks of counseling or psychotherapy if that person does not want to know? Explain.

3. What methods of structuring the review of informed consent information do you think are best? Why?

4. Can there ever be truly informed consent in court-mandated situations? If you think not, can a professional ethically conduct such counseling? Explain.

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