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SUPPLEMENTAL INFORMED CONSENT Orthodontic Treatment in the Era of COVID19Thank you for your continued trust in our practice. As with the transmission of any communicable disease like a cold or the
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How to fill out supplemental informed consent

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Step 1: Begin by reviewing the main informed consent form.
02
Step 2: Identify the specific additional information or procedures that require further consent.
03
Step 3: Create a separate supplemental informed consent form that includes the necessary details.
04
Step 4: Clearly explain the purpose, risks, benefits, and alternatives of the additional information or procedures in the form.
05
Step 5: Leave space for the participant to provide their signature and date.
06
Step 6: Provide the participant with enough time to read and understand the supplemental informed consent form.
07
Step 7: Ensure that all questions and concerns of the participant are addressed before they sign the form.
08
Step 8: Obtain the participant's signature and date on the supplemental informed consent form.
09
Step 9: Keep a copy of the signed form for both the participant's and researcher's records.
10
Step 10: Ensure that the participant receives a copy of the signed supplemental informed consent form.

Who needs supplemental informed consent?

01
Supplemental informed consent is typically needed when there are additional information or procedures beyond what is covered in the main informed consent form.
02
This can include situations where new risks or benefits emerge during the course of a study, or when a participant's consent is required for additional procedures or changes in the study protocol.
03
In general, anyone participating in a research study that involves such circumstances would need to provide supplemental informed consent.
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Supplemental informed consent is a document that provides additional information or updates to an existing informed consent form.
Anyone involved in a research study or clinical trial that requires additional information or updates to the original informed consent.
Supplemental informed consent forms are typically filled out by the research team or healthcare providers involved in the study and must be signed by the participant.
The purpose of supplemental informed consent is to ensure that participants are fully informed about any changes or updates to the study and can make an informed decision about continuing to participate.
Supplemental informed consent forms may include information about new risks, procedures, or updated study protocols that were not included in the original consent form.
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