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Consent to Participate in Research A Randomized Control Trial for Substance Use Problems Introduction You are being asked to participate in a research study conducted by Dr. Kent A. Kiel who is the
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Read the consent form carefully and make sure you understand all the information provided.
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Fill out your personal information such as your name, address, and date of birth.
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Who needs consent to participate in?

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Anyone who is planning to participate in a research study, clinical trial, or any other type of activity that requires formal consent.
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Consent to participate refers to an individual's agreement to take part in a particular activity, often related to research studies or clinical trials, indicating that they understand the nature and risks of participation.
Researchers and organizations conducting studies or activities that involve human subjects are required to file consent to participate in.
To fill out consent to participate, individuals should read the document carefully, understand the information provided, and sign where indicated to confirm their agreement.
The purpose of consent to participate is to ensure that individuals are fully informed about the activities they are participating in and to protect their rights and welfare.
Information such as the study's purpose, procedures, risks, benefits, confidentiality, and the participant's rights must be reported on the consent to participate document.
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