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Appendix F: Recruitment Confirmation Emails/LettersTenant Recruitment Confirmation Email/Letter Thank you for agreeing to participate in the evaluation of the Small Area Fair Market Rent Demonstration,
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How to fill out getting informed consent for

01
Start by introducing yourself and explaining your role in the consent process.
02
Provide a brief overview of the purpose and nature of the research or procedure.
03
Clearly explain the risks and benefits involved, including any potential side effects.
04
Use clear and simple language to ensure the participant understands the information.
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Give the participant enough time to ask questions and clarify any doubts.
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Obtain written consent by having the participant sign the consent form.
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Provide a copy of the signed consent form to the participant for their records.
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Ensure that the participant understands their right to withdraw from the study at any time.
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Continually communicate and update the participant about any changes or new information that may arise during the study.
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Respect the participant's autonomy and ensure their voluntary participation throughout the process.

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Getting informed consent is necessary for any research study or medical procedure involving human participants.
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It is required in both medical and non-medical fields to ensure ethical standards and protect the rights of individuals.
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Researchers, doctors, healthcare professionals, scientists, and anyone involved in conducting studies or experiments on humans need to obtain informed consent.
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This includes clinical trials, surveys, interviews, experiments, observational studies, and any other research that involves human subjects.

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Informed consent is obtained to ensure that individuals are fully aware of the risks and benefits associated with a particular action or decision before giving their consent.
Those who are conducting research or providing medical treatment are required to obtain informed consent from the participants or patients involved.
To fill out informed consent forms, individuals must clearly explain the purpose of the research or treatment, as well as the risks and benefits involved. Participants must also sign the form to indicate their understanding and agreement.
The purpose of obtaining informed consent is to protect individuals' autonomy and ensure that they are able to make informed decisions about their participation in research or medical treatment.
Informed consent forms must include information about the purpose of the research or treatment, potential risks and benefits, confidentiality measures, and the individuals' rights as participants.
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