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Synergy Health 1151 West Main Street Richmond, VT 05477 8024345437INFORMED CONSENT I have received information about my condition and proposed chiropractic treatment program as well as alternative
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Read the informed consent document thoroughly to understand the purpose, procedures, risks, and benefits of the study or activity.
02
Discuss any concerns or questions with the person in charge of administering the informed consent.
03
Provide any necessary personal information or medical history as requested.
04
Sign and date the informed consent document to indicate your understanding and agreement to participate.
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Keep a copy of the signed informed consent form for your records.
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If there are any changes or updates to the study or activity, make sure to receive and review any revised informed consent forms.
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If you have any further questions or concerns during the study or activity, reach out to the person in charge for clarification or assistance.

Who needs informed consent i have?

01
Anyone who is being asked to participate in a research study or any activity that involves potential risks or benefits should be provided with an informed consent form. This includes individuals of legal age, individuals with decision-making capacity, and individuals who have been fully informed about the study or activity in question. Informed consent ensures that individuals have the opportunity to make an informed and voluntary decision regarding their participation.
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Informed consent is a process where a patient or participant agrees to undergo a specific medical treatment or participate in a research study after being informed of the risks, benefits, and alternatives.
Healthcare providers, researchers, and medical facilities are required to file informed consent forms.
Informed consent forms are typically provided by the healthcare provider or research team and should be filled out by the patient or participant with all the required information.
The purpose of informed consent is to ensure that patients or participants have a full understanding of the treatment or study they are agreeing to, including the potential risks and benefits.
Informed consent forms typically include information about the treatment or study, risks and benefits, alternatives, confidentiality, and the right to withdraw consent.
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