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The MURDOCK Study Community Registry and Biorepository is a large-scale longitudinal cohort study involving 12,526 participants from Kannapolis, North Carolina. The study collects comprehensive health data, blood and urine samples, and integrates electronic health records to facilitate research on various medical conditions and participant health changes over time. The study aims to enhance our understanding of health outcomes and disease prevention in the Southeastern U.S.
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01
Visit the Murdock Study Community Registry website.
02
Click on 'Register' to create a new account.
03
Provide personal information such as your name, email address, and date of birth.
04
Complete health-related questions accurately.
05
Review and agree to the terms and conditions.
06
Submit your registration form.
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Check your email for a confirmation link and click on it to verify your account.
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Log in to your account and update your profile if necessary.

Who needs murdock study community registry?

01
Individuals interested in participating in health research studies.
02
Community members looking to contribute to advances in medical research.
03
Researchers seeking a diverse population for studying health issues.
04
Healthcare providers aiming to connect with patients in research initiatives.
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The MURDOCK Study Community Registry is a database designed to collect and manage information related to participants in the MURDOCK Study, which aims to better understand health issues and improve health outcomes in a defined community.
Individuals or organizations involved in the MURDOCK Study, including researchers and healthcare providers, are required to file the MURDOCK Study Community Registry to ensure compliance with study protocols and data collection standards.
To fill out the MURDOCK Study Community Registry, participants need to provide required personal information, health history, and consent forms as instructed by the study guidelines, typically done via an online portal or paper forms.
The purpose of the MURDOCK Study Community Registry is to facilitate the collection of data for research purposes, promote participant engagement, and create a comprehensive dataset that supports health-related research within the community.
Information that must be reported includes participant demographics, health conditions, consent status, and any relevant medical history as specified by the study requirements.
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