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FOLLOWUP SURVEY INFORMED CONSENT INTRODUCTION You are invited to participate in Followup Survey process upon being discharged from Substance Use Disorder (SUD) Treatment. The decision to complete
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How to fill out follow-up survey informed consent:

01
Read the consent form carefully: Start by thoroughly reading the follow-up survey informed consent form. Make sure you understand the purpose of the survey, what information will be collected, and how it will be used.
02
Provide necessary personal information: Fill in all the required personal information accurately. This may include your name, contact details, age, gender, and any other demographic information that is relevant to the survey.
03
Understand the risks and benefits: Take the time to review any potential risks or benefits associated with participating in the follow-up survey. This could include the possibility of emotional discomfort, privacy concerns, or potential benefits such as contributing to valuable research.
04
Ask questions if needed: If there is anything in the follow-up survey informed consent form that you don't understand or need clarification on, don't hesitate to ask questions. It is essential that you have a clear understanding of what you are consenting to.
05
Provide informed consent: After reviewing the form and understanding its content, you can give your informed consent by signing and dating the document. This signifies that you agree to participate in the follow-up survey and understand the terms outlined in the consent form.

Who needs follow-up survey informed consent:

01
Researchers: Researchers conducting a follow-up survey generally require informed consent from participants. This ensures that participants understand the purpose of the survey and are willing to provide the necessary information.
02
Participants: Individuals who agree to participate in a follow-up survey should also provide informed consent. This gives them the opportunity to understand what their involvement entails and make an informed decision about whether they want to take part.
03
Institutional Review Boards (IRBs): In some cases, an IRB may also require researchers to obtain informed consent for follow-up surveys. IRBs review research proposals to ensure ethical standards are met, including obtaining informed consent from participants.
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Follow-up survey informed consent is a document that participants sign to agree to participate in a follow-up survey after the initial study.
Researchers conducting a study that includes a follow-up survey are required to obtain and file follow-up survey informed consent from participants.
Follow-up survey informed consent can be filled out by clearly explaining the purpose of the follow-up survey, potential risks and benefits, and obtaining signatures from participants.
The purpose of follow-up survey informed consent is to ensure that participants are fully informed about the follow-up survey, including its purpose, risks, benefits, and their rights as participants.
Follow-up survey informed consent must include details about the study, purpose of the follow-up survey, risks and benefits, confidentiality assurances, participant rights, and contact information for questions or concerns.
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