Glucose Empowerment Through Monitoring and Social Support in Pregnancy
Recruiting
N/A
Interventional Study
Pregnancy, Complications
Gestational Diabetes
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 70 (estimated)
- Sponsor
- Tufts Medical Center · Other
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About This Trial
The purpose of the research is to learn whether wearing a continuous glucose monitor that shows blood glucose levels in real time on a smart phone app and participating in a group chat with other research participants will help participants keep a healthy blood glucose level during pregnancy.
High levels of blood glucose during pregnancy can lead to health problems during and after pregnancy. It …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pregnant (\<20w0d)
* At least 18 years to 45 years old
* BMI \>25, personal history of GDM, or first-degree family member with type II diabetes
* Comfortable conversing in English
* Own a smartphone and willing to use the CGM app and Signal
* Receiving prenatal care and planni…
Contacts