Evaluating the Feasibility of Using M-Health to Improve Serum Glucose Logs

Completed · Not applicable

Conditions studied: Gestational Diabetes Mellitus

In brief

Gestational diabetes mellitus (GDM) can cause adverse outcomes for the mother and fetus due to hyperglycemia. The purpose of this study is to evaluate the feasibility of improving pregnant women's glucose logs using a Bluetooth enabled glucose monitor and associated mobile health application and to assess their satisfaction with using mobile health technology.

Key facts

Study ID

NCT03340311

Run by

Leslie Balcazar De Martinez

People needed

8

Starts

2017-11-01

Expected to finish

2018-04-28

Last updated by the study team

2018-05-01

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• At least 18 years old
• Willing and able to give informed consent
• Diagnosis of gestational diabetes
• Speak English and/or Spanish
• Have ownership of a smartphone capable of running the mobile health application
• Willing to download the iGluco mobile phone application

You may not qualify if…

• Have knowledge that their delivery will occur prior to completion of the required eight weeks of glucose logs
• Possess a Bluetooth enabled glucometer

Where it is running

• University of Virginia Maternal Fetal Medicine Clinic — Charlottesville, Virginia, United States

Full record on ClinicalTrials.gov

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