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Main Study Informed Consent Form and HIPAA Authorization Study Title:Occipital Nerve Blocks for Acute Treatment of Pediatric MigraineVersion Date:October 04, 2018Principal Investigator:Dr. Christina
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Read the entire study informed consent form carefully.
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Make sure you understand all the information provided in the form.
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Fill out all required fields accurately.
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Ask any questions you may have before signing the form.
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Sign and date the form to indicate your consent to participate in the study.

Who needs study informed consent form?

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Anyone who is invited to participate in a research study or clinical trial needs to fill out a study informed consent form.
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In some cases, legal guardians may need to fill out the form on behalf of minors or individuals who are unable to provide informed consent themselves.
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Study informed consent form is a document that explains the details of a research study to participants, including the risks and benefits, and allows them to make an informed decision about whether or not to participate.
Researchers conducting a study are required to provide participants with a study informed consent form.
Study informed consent forms should be filled out by including all necessary information about the study, risks, benefits, and providing space for participants to sign indicating their understanding and agreement.
The purpose of study informed consent form is to ensure that participants are fully informed about the research study and to obtain their voluntary agreement to participate.
Study informed consent forms must include information about the study objectives, procedures, risks, benefits, confidentiality, voluntary participation, and contact information for questions or concerns.
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