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INFORMED CONSENT
Lisa B. Anderson, MOM, Dial. OM, Lac
Courtney Smith, Mac., Dial. Ac, Lac
I hereby request and consent to the performance of acupuncture treatments and other procedures
within the
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01
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02
Start by reading the consent form carefully and make sure you understand its contents.
03
Provide your personal information such as name, age, address, and contact details.
04
Sign and date the form to acknowledge your understanding and agreement.
05
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Return the original form to the appropriate party as instructed.
Who needs clarifying informed consentashrminformed consent?
01
Clarifying informed consent is needed by any individual who is being asked to participate in a study, research, medical procedure, or any situation where their consent is required.
02
It ensures that individuals fully understand the purpose, risks, benefits, and alternatives related to the activity they are consenting to.
03
This includes patients, research participants, volunteers, or anyone who may be affected by the outcome of the consented activity.
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What is clarifying informed consent?
Clarifying informed consent refers to the process of ensuring that individuals fully understand the information presented to them before agreeing to participate in a study or treatment. This involves providing clear explanations of the purpose, risks, benefits, and alternatives.
Who is required to file clarifying informed consent?
Researchers and institutions conducting studies involving human participants are typically required to file clarifying informed consent to ensure compliance with ethical guidelines and legal regulations.
How to fill out clarifying informed consent?
To fill out clarifying informed consent, individuals must provide comprehensive information about the study, including its purpose, procedures, potential risks, benefits, and the participant's right to withdraw at any time without penalty. Additionally, both the researcher and participant must sign the document.
What is the purpose of clarifying informed consent?
The purpose of clarifying informed consent is to protect the rights and welfare of participants by ensuring that they are fully informed about what their participation entails and that they voluntarily agree to it.
What information must be reported on clarifying informed consent?
Information that must be reported includes the study's purpose, duration, procedures, risks and benefits, confidentiality assurances, and contact information for questions or concerns.
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