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SUPPLEMENTAL INFORMED CONSENT Orthodontic Treatment in the Era of COVID-19 Thank 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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Step 1: Obtain a copy of the supplemental informed consent form.
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Step 2: Read and understand the main informed consent form for the study.
03
Step 3: Identify the additional information or procedures that require supplemental informed consent.
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Step 4: Fill in the necessary details on the supplemental informed consent form.
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Step 5: Review the completed form for accuracy and completeness.
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Step 6: Sign and date the form, indicating your agreement to the supplemental informed consent.
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Step 7: Return the signed form to the appropriate party or entity involved in the study.

Who needs supplemental informed consent?

01
Supplemental informed consent is needed by individuals participating in research studies or clinical trials where additional information or procedures are being introduced after the initial informed consent has been obtained.
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Supplemental informed consent is additional consent obtained after the initial consent for research or medical treatment, typically to inform participants of new information or changes in the study.
Researchers, medical professionals, or institutions conducting studies or treatments requiring additional consent from participants.
Supplemental informed consent forms are typically filled out by the participant or their legal guardian, with the assistance of the researcher or medical professional.
The purpose of supplemental informed consent is to ensure that participants are fully informed of any new information or changes in a study or treatment, allowing them to make an updated decision on their participation.
Supplemental informed consent forms should include details of the new information or changes, potential risks or benefits, and any updated procedures or requirements.
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