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Informed Consent Addendum For Tell Psychotherapy This is to be used in conjunction with the Informed Consent document that is required of all clients prior to starting therapy services, What is Tell
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How to fill out informed consent addendum for

01
Step 1: Obtain the informed consent addendum form from the appropriate source.
02
Step 2: Read the instructions and requirements stated in the addendum form carefully.
03
Step 3: Fill out the introductory portion of the addendum form, which usually includes the study title, principal investigator's name, and date.
04
Step 4: Provide a detailed explanation of the changes or additions being made to the original informed consent document. Clearly state the reasons for these modifications.
05
Step 5: Include any new risks, benefits, or alternatives that need to be communicated to the participants as part of the addendum.
06
Step 6: Ensure that the addendum includes a space for the participant's signature and date, confirming their agreement to the revised information.
07
Step 7: Review the completed addendum form for accuracy and completeness.
08
Step 8: Submit the filled-out informed consent addendum form to the designated person or authority as instructed.

Who needs informed consent addendum for?

01
Anyone who is already participating in a study that requires an informed consent document may need an addendum. The addendum becomes necessary when there are changes or additions to the original information provided to the participants. This ensures that the participants are kept informed and have the opportunity to reconsider their participation based on the revised details.
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The informed consent addendum is used to update or modify the original informed consent document.
Research participants and researchers are required to file informed consent addendum.
To fill out the informed consent addendum, participants and researchers must review the original informed consent document and make any necessary changes or updates.
The purpose of the informed consent addendum is to ensure that research participants are fully informed of any changes to the study protocol or procedures.
The informed consent addendum must report any changes to the study protocol, procedures, risks, benefits, or any other relevant information.
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