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This document is a consent form for a research study aimed at understanding barriers to the adoption of continuous glucose monitoring (CGM) devices among adults with type 1 diabetes (T1D). The study will provide support and supplies for a duration of one year and aims to assess the effectiveness of an intervention called ONBOARD. Participants will undergo assessments and provide data related to their diabetes management throughout the study.
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How to fill out med_survey_consent rev072020

01
Read the entire consent form carefully.
02
Fill in your personal information as requested, including name, date of birth, and contact details.
03
Review the purpose of the survey and how your data will be used.
04
Understand your rights regarding privacy and data protection.
05
Sign and date the consent form at the designated section.
06
Submit the completed consent form as instructed.

Who needs med_survey_consent rev072020?

01
Participants of the medical survey who are at least 18 years old.
02
Individuals who have been invited to take part in the survey.
03
Anyone who wishes to provide valuable health data for research purposes.
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Med_survey_consent rev072020 is a document that provides consent for individuals to participate in a medical survey, outlining the terms and conditions of participation.
Individuals participating in the medical survey and organizations conducting the survey are required to file med_survey_consent rev072020.
To fill out med_survey_consent rev072020, individuals must provide personal information as requested, read the consent terms, and sign the document to confirm their agreement.
The purpose of med_survey_consent rev072020 is to ensure that participants are informed about the survey and its implications, and to obtain their voluntary consent.
The information that must be reported includes participant identification details, acknowledgment of understanding the survey's purpose, risks, and benefits, and consent to participate.
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Relevant keywords

diabetes continuous glucose monitoring type 1 diabetes ONBOARD intervention research study Molly Tanenbaum hemoglobin A1c CGM devices patient consent clinical trial

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