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ASHLEY HUDSON, LCSW, LLC 2039 Regency Road, Suite 1 Lexington, KY 40503 8594921090 (phone) 8592023640 (fax) ashleyhudsonlcsw@gmail.comInformed Consent and Permission to Treat Client Name: ___1. Qualifications
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Begin by providing the participant with a clear explanation of the study and its purpose.
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Make sure the participant understands their rights and responsibilities as a study participant.
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Clearly outline the risks and benefits of participating in the study.
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Who needs informed consent and permission?

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Researchers conducting studies that involve human participants require informed consent and permission.
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Minors and individuals who may not have the capacity to fully understand the study also require permission from a legal guardian or authorized representative.
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Informed consent is the process of obtaining permission from an individual to participate in a study or project after providing them with all the relevant information.
Researchers, doctors, or anyone conducting a study or project involving human subjects are required to file informed consent and permission.
Informed consent forms are typically filled out by the researcher or project leader and must include all relevant information about the study or project.
The purpose of informed consent and permission is to ensure that individuals are aware of the risks and benefits of participating in a study or project and that they voluntarily agree to take part.
Informed consent and permission forms must include information about the study objectives, procedures, risks, benefits, confidentiality, and the right to withdraw.
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