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Three basic principles, among those generally accepted in our cultural tradition, are particularly relevant to the ethics of research involving human subjects: the principles of respect of persons, beneficence and justice.
The underlying principle of consent isn't particularly complicated: Patients have a right to make an informed, voluntary decision about their care. That means they need to know the nature, risks, and benefits of their options ? which includes declining treatment.
Informed consent is the process in which a health care provider educates a patient about the risks, benefits, and alternatives of a given procedure or intervention. The patient must be competent to make a voluntary decision about whether to undergo the procedure or intervention.
Types of consent include implied consent, express consent, informed consent and unanimous consent.
Informed Consent Essentials Consent must be given voluntarily. The client must be competent (legally as well as cognitively/emotionally) to give consent. We must actively ensure the client's understanding of what she or he is agreeing to. The information shared and all that is agreed to must be documented.
Four core criteria must be met: the patient giving consent must have capacity ? the consent must be freely given ? the consent must be sufficiently specific to the procedure or treatment proposed ? the consent must be informed.
I will make every attempt to inform you in advance of planned absences, and provide you with the name and phone number of the mental health professional covering my practice. If you are unhappy with what is happening in therapy, I hope you will will talk with me so that I can respond to your concerns.
There are 4 components of informed consent including decision capacity, documentation of consent, disclosure, and competency. Doctors will give you information about a particular treatment or test in order for you to decide whether or not you wish to undergo a treatment or test.