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INFORMED CONSENT ADDENDUM: ELEMENTAL HEALTH THERAPY The following information is provided to clients who are seeking elemental health therapy. This document covers your rights, risks, and benefits
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Who needs informed consent addendum for?

01
Researchers conducting a study or research project that requires informed consent from participants.
02
Participants or subjects involved in a study who are required to provide informed consent.
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Institutional review boards or ethics committees overseeing research projects.
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Any individuals or entities involved in the research process who need a legally binding document to record modifications or updates to the initial informed consent.
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It is a form used to add additional information or updates to an existing informed consent document.
Researchers and study coordinators who need to update the informed consent document for a clinical trial or research study.
The addendum should be filled out with the new information, signed and dated by the appropriate parties, and attached to the original informed consent document.
The purpose is to ensure that participants are fully informed of any changes to the study or potential risks before continuing their participation.
Any new information, updates, or changes to the study protocol, risks, benefits, or procedures that could impact the participant's decision to continue in the study.
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