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TO:Prospective Researchers/InvestigatorsFROM:MESAS PREDATE:January 21, 2019SUBJECT: Sample Informed Consent Template Tennessee Department of Mental Health and Substance Abuse Services Institutional
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How to fill out sample informed consent template

01
To fill out a sample informed consent template, follow these steps:
02
Begin by reading through the entire template to understand its contents.
03
Start by providing information about the study or research project for which the informed consent is being obtained.
04
Include a section explaining the purpose of the study and what participation entails.
05
Clearly state any potential risks or benefits associated with participation and ensure that they are explained in a comprehensible manner.
06
Include a section on confidentiality and how participant data will be handled and stored.
07
Provide a section that outlines the participant's rights and options for withdrawing consent at any time.
08
Clearly state the contact information of the principal investigator or researcher in case participants have any questions or concerns.
09
Include a space for the participant's signature, as well as the date of signing.
10
Make sure to provide an additional copy of the filled-out consent form to the participant.
11
Finally, ensure that the consent form is written in plain and easily understandable language, avoiding excessive technical jargon.

Who needs sample informed consent template?

01
A sample informed consent template is needed by researchers, scientists, medical professionals, and anyone conducting a study or research project that involves human participants. It is essential for ensuring that participants understand the purpose of the study, the risks and benefits involved, and their rights as participants.
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The sample informed consent template is a document that outlines the information provided to research participants, ensuring that they understand the nature of the study and their involvement, and that they voluntarily agree to participate.
Researchers conducting studies that involve human subjects are required to file a sample informed consent template.
To fill out a sample informed consent template, researchers must provide detailed information about the study, risks and benefits, confidentiality, and participant rights, among other things.
The purpose of the sample informed consent template is to protect the rights and welfare of research participants by ensuring that they are fully informed about the study before agreeing to participate.
The sample informed consent template must include information about the study procedures, risks and benefits, confidentiality, voluntariness of participation, and contact information for questions or concerns.
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