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COVER PAGE Title of Study: Home Blood Pressure Monitoring Intervention for Self-management of High Blood Pressure Among Alaska Native People NCT number: NCT03872856 Date of Document: July 9, 2021FleschKincaid
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Start by reading and understanding the consent form carefully.
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Who needs consent form research study?

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Anyone who is participating in a research study or clinical trial needs to fill out a consent form. This includes both adults and minors, as their legal guardians or parents need to provide consent on their behalf. Consent forms ensure that participants understand the purpose, risks, benefits, and any other relevant information about the study before agreeing to participate.
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A consent form in a research study is a document that provides potential participants with information about the study, allowing them to understand the risks, benefits, and their rights before agreeing to participate.
Researchers conducting studies that involve human subjects are required to file consent forms to ensure participants are informed about the study and voluntarily agree to participate.
To fill out a consent form, researchers must provide clear information about the study's purpose, procedures, risks, benefits, confidentiality, and the voluntary nature of participants' involvement. Participants then sign to indicate their understanding and agreement.
The purpose of the consent form is to ensure that participants are fully informed about the research study, understand their rights, and willingly agree to participate, thereby upholding ethical standards in research.
The consent form must include the study's purpose, procedures, potential risks and benefits, confidentiality measures, details on voluntary participation, and contact information for questions.
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