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Digital Natural History Studies with Citizen

A natural history study follows a group of people over time who have a specific disease, collecting health information in order to understand how the disease develops and changes and how to diagnose and treat it better.

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Rare Patient Network

powered by Citizen Health

The GLUT1 Deficiency Foundation has partnered with Citizen Health, which powers next generation digital Natural History Studies that organize, summarize and store patient medical record information obtained from multiple hospitals and providers.

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Important information that can accelerate research is often trapped in medical records. As a patient or parent/guardian, you can unlock those records and contribute them to research in a private and secure way.

Citizen generates natural history study data that uses medical records across multiple hospitals and providers where a participant has been seen, rather than patient/parent/caregiver reported data (like our Matrix study) to collect meaningful information on how GLUT1 Deficiency has affected a person’s life.

INSIGHTS FROM PARENTS

learn more below

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Citizen Health benefits

  • Participation is completely digital
  • Collects participants’ medical records from all institutions visited and organizes, digitizes, and summarizes them in a secure online account at no cost to you and under your full control
  • Having all medical records in one place helps you have a better understanding of your medical history and inform future decisions
  • Easily share your records to collaborate with your medical team, seek second opinions, and coordinate with caregivers
  • With your consent, clinicians, researchers and biopharma can access anonymized data to aid in research
  • You can have a big impact on research with minimal effort

 you are the experts.

 you can help best tell the story of GLUT1 Deficiency.

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NATURAL HISTORY STUDY

Quick Start Guide

Use this easy reference to help you get started using your power to shape the future for GLUT1 Deficiency patients.

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1

Get ready to enroll:

  • You'll need less than 10 minutes to complete the sign up
  • You'll need a phone or a computer with a working camera
  • You'll need a driver's license or other form of ID
  • You'll need an email address and will choose a password
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Other information you'll need:

  • Names of all doctors who have treated your child
  • Names of medical institutions where you child has received care
    *there's space to enter two in the initial setup process, but you can go back and enter as many as you would like once the account is set up
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Clues for certain questions:

  1. What gene is affected?  
    Answer:  SLC2A1
  2. What is the primary diagnosis?
    Answer:  GLUT1 deficiency (SLC2A1)
  3. Institute that diagnosed the condition? 
    Answer:  write the hospital that did the lumbar puncture or genetic testing that gave you the diagnosis
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How it works:

  1. Create your patient’s account
    Click the “JOIN NOW” button, then enter an email, name, and password.

  2. Citizen collects patient’s health record for you
    Once you add patient details, over the next 30-60 days, they will obtain the entire Electronic Health Records (EHR) and add them to the patient’s Citizen account.
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reach out to the GLUT1 Deficiency Foundation if you'd like to schedule one-to-one assistance
with the enrollment process or have questions

FAQ - Citizen Natural History Study

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learn more about the importance of natural history studies in this publication