Gestational Diabetes Clinical Trial
Official title:
Group and Mobile Care for Gestational Diabetes
NCT number | NCT03026218 |
Other study ID # | HP-00071275 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 15, 2017 |
Est. completion date | May 15, 2019 |
Verified date | March 2022 |
Source | University of Maryland, Baltimore |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A critical variation in the provision of prenatal care to women with GDM is the need to keep patients engaged with their care between visits by tracking glucose levels using finger sticks and making dietary and other lifestyle modifications to keep these levels at or close to normal. Multiple studies have demonstrated that the use of mobile devices can improve medical outcomes. In order to keep patients engaged between appointments and improve self-care/lifestyle, we will study the use of a glucose monitoring system with nutrition therapy called GlucoseMama(GM). GM is a mobile app on the iOS system that individuals with GDM will use to tract blood sugars and number of carbs consumed. In addition, it will give the user positive feedback and rewards for using the system. This model of group care with mobile phone monitoring and reminders for women with GDM has not been previously studied. A randomized control trial is purposed to determine if this approach improves patient care. The investigators hypothesize that group prenatal care along with inter-session mobile therapy will increase dietary compliance and therefore reduce the number of individuals requiring pharmacologic therapy and improve neonatal outcomes during pregnancy. Group prenatal care (GPC) will provide a community foundation to improve learning and increase the motivation of patients to learn and change. This motivation will be further strengthened by the use of the GlucoseMama monitoring system which will provide each patient with glucose tracking and individualized nutritional support.
Status | Completed |
Enrollment | 22 |
Est. completion date | May 15, 2019 |
Est. primary completion date | October 15, 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 51 Years |
Eligibility | Inclusion Criteria: - Diagnosis of Gestational Diabetes - Planning on delivering at home institution Exclusion Criteria: - Unwilling to participate. |
Country | Name | City | State |
---|---|---|---|
United States | University of Maryland, Baltimore | Baltimore | Maryland |
Lead Sponsor | Collaborator |
---|---|
University of Maryland, Baltimore |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduction in the number of individuals requiring pharmacotherapy for treatment of gestational diabetes | 2 years | ||
Secondary | Reduction in the number of neonates born large for gestational age. | 2 years | ||
Secondary | Increased number of individuals who are screened in the postpartum period for type 2 diabetes. | 2 years | ||
Secondary | Reduction in the number of infants with neonatal hypoglycemia. | 2 years |
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