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What are the elements of a valid consent?

What is informed consent?

Is patient/client consent required in all service settings?

Does consent have to be written?

How does one document consent?

Do I need to speak to or meet with the patient/client or substitute decision-maker to obtain consent?

How does one judge a person to be capable?

Must patients/clients be informed of their incapacity?

What is the process for challenging a finding that a person has been found incapable?

What is the hierarchy of substitute decision makers?

What are the criteria for qualifying as a substitute decision maker?

How do you determine who the highest ranking substitute decision maker is?

Are there any guidelines for substitute decision makers?

What do I do if I feel that the substitute decision maker is not acting in the best interests of the incapable person?

Can I provide a service without consent?

When am I liable?

Can I assume that, since patients/clients call for appointments and come to my office, they are consenting to my services?

In my work setting, I see patients/clients who appear to be incapable of providing valid consent, for a variety of reasons. When I try to reach the substitute decision maker (SDM) to make a decision on behalf of the patient/client, I am often not successful in reaching the SDM. Can I proceed with the service?

How can I obtain consent from a person who has significant communication difficulties?

If I am seeing patients/clients over a period of years, how often do I have to obtain their consent for services? Am I required to obtain consent every time there is a slight change in the services I am providing?

What is the difference between a power of attorney and a substitute decision maker?