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INFORMED CONSENT The following information is provided to acquaint you with the procedures of this office and to better assist you in your efforts towards personal growth. I. Your Rights as a Client
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Informed consent is a process for getting permission before conducting a healthcare intervention on a person.
Healthcare providers and researchers are required to obtain informed consent before conducting any healthcare intervention or research study.
To fill out informed consent, the healthcare provider or researcher must explain the purpose of the intervention, risks and benefits, alternative treatments, and ensure the individual fully understands before obtaining their signature.
The purpose of informed consent is to protect the autonomy and rights of individuals by ensuring they are fully informed about the healthcare intervention or research study before giving their consent.
Informed consent must include information about the purpose of the intervention, risks and benefits, alternative treatments, confidentiality, and the right to refuse or withdraw consent.
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