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APPROVED BY INTERVIEW IRB JUNE 29, 2020, Informed Consent Form TITLE OF STUDY:EVALUATION OF A PATIENTCENTERED APPROACH TO COLLECTING ELECTRONIC MEDICAL RECORD DATA FOR AN OBSERVATIONAL, NATURAL HISTORY
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Read the lupus informed consent form thoroughly to understand all the information provided.
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Fill out personal information accurately, including name, date of birth, contact information, etc.
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Check boxes or provide answers to all questions on the form.
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Sign and date the form to acknowledge your understanding and agreement with the information provided.
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Ask any questions or seek clarification from the healthcare provider if needed before submitting the form.

Who needs lupus informed consent form?

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Patients who are diagnosed with lupus and are considering participating in a clinical trial or research study related to lupus treatment.
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The lupus informed consent form is a document provided to patients participating in lupus research studies, outlining the risks and benefits of participation.
Patients who are participating in lupus research studies are required to fill out the lupus informed consent form.
Patients must read the form carefully, ask any questions they may have, and then sign the form to indicate their consent to participate in the study.
The purpose of the lupus informed consent form is to ensure that patients are fully informed about the study they are participating in, and to obtain their consent to participate.
The lupus informed consent form must include information about the study, risks and benefits of participation, confidentiality, and the patient's rights.
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