The Hoosier Moms Cohort !@#$%^*()_+{}|:"?`-=[]/~abcdefghijklmnopqrstuvwxyzABCDEFGHIJKLMNOPQRSTUVWXYZ1234567890 end

  • STATUS
    Recruiting
Send
Updated on 29 April 2024

Summary

The purpose of this study is to better understand how Gestational Diabetes Mellitus (GDM, high blood sugar in pregnancy) develops. We hope to understand the differences between women who are diagnosed with GDM and those who are not. Another purpose is to understand how GDM can progress to Type 2 Diabetes after the baby is born. We also hope to learn about infants born to mothers with GDM compare to infants born to mothers not diagnosed with GDM.
 
This study is taking place currently in Indianapolis, Bloomington, and Evansville, Indiana. 

Description

As part of Indiana University Grand Challenges Precision Health Initiative Diabetes Team, this prospective cohort study seeks to better understand and identify differences in women who develop gestational diabetes mellitus (GDM) between those who don't.
 
Participants will be asked to come for up to 5 in person visits; three during pregnancy and two after you deliver your baby.  At these visits, participants will be asked to provide blood and urine, answer questions about their pregnancy and health, and take surveys.  Participants will be given an activity monitor to wear (like a Fitbit) and will be asked to download a nutrition app to take photos of what they eat.
 
 
Participants will be compensated for their participation.

Details
Condition gestational diabetes mellitus,pregnancy,diabetes,gestational diabetes,pregnant,mom,type 1,type I,type 2,type II, hoosier mom, hoosier, mom, pregnancy study,
Age 18years - 100years
Clinical Study IdentifierTX9361
Last Modified on29 April 2024

Eligibility

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Preferred way of contact label
Race
Ethnicity
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.