Randomized Control Trial to Investigate the Effect of a Smartphone Application for Gestational Diabetes Management on Postpartum Glucose Intolerance
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Tufts Medical Center
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Malama app as intervention
Study Overview
Brief Summary
Without intervention, approximately 70% of women diagnosed with GDM will develop type 2 diabetes mellitus in their lifetime. Abnormal results of a 2 hour oral glucose tolerance test (OGTT) performed as early as 2 days postpartum are predictive of impaired glucose tolerance 1 year postpartum. The investigators hypothesize that use of the Malama smartphone application to optimize antenatal glycemic control will result in lower incidence of postpartum glucose intolerance, which may decrease long term risk of progression to diabetes mellitus.
Detailed Description
The effect of smartphone applications for gestational diabetes management on risk of postpartum glucose intolerance, antenatal glycemic control, and other perinatal outcomes is unknown.
This study is a randomized control trial in which patients diagnosed with gestational diabetes will be randomized to use of the Malama app vs. standard care as described above.
The primary aim of the study is to investigate if the incidence of postpartum glucose intolerance is lower in patients using the Malama app for gestational diabetes management compared to patients receiving standard care.
Secondary outcomes that will be investigated include several markers of maternal and neonatal perinatal morbidity. Maternal outcomes that will be investigated include postpartum hemoglobin A1c level, interval pregnancy weight gain, incidence of hypertensive disorders of pregnancy, cesarean delivery, operative delivery, postpartum hemorrhage, and advanced perineal lacerations. Neonatal secondary outcomes include gestational age at delivery, birthweight and incidence of large for gestational age infants, shoulder dystocia, NICU admission, length of NICU stay, neonatal blood glucose nadir, and need for neonatal IV glucose support.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Pregnant women receiving prenatal, delivery, and postpartum care at Tufts Medical Center
- •Gestational diabetes diagnosed between 14 0/7 and 31 6/7 weeks gestation on basis of 1-hour glucose challenge test result of >=200 mg/dL or Carpenter-Coustan criteria
- •>= 18 years of age
- •Literate in English or Spanish (?additional languages pending app translation)
- •Access to or ownership of a smartphone compatible with Malama
- •Willing and able to sign the informed consent
Exclusion Criteria
- •Unable to tolerate oral glucose tolerance test (i.e. history of gastric bypass surgery)
- •Diagnosis of pregestational diabetes
- •Prescribed medications for chronic disease that affect glucose metabolism (e.g., long term oral steroids)
- •Does not own smartphone compatible with Malama application
- •Severe life-limiting fetal anomaly
Arms & Interventions
Malama Arm
Participants enrolled in this arm will agree to using the Malama app to track glycemic management.
Intervention: Malama App (Behavioral)
Control
Participants enrolled in this arm agree to standard management (FS log on phone, notebook, etc)
Outcomes
Primary Outcomes
Malama app as intervention
Time Frame: 8-26 weeks
The primary aim of the study is to investigate if the incidence of postpartum glucose intolerance is lower in patients using the Malama app for gestational diabetes management compared to patients receiving standard care.
Secondary Outcomes
- Postpartum hemoglobin A1c level(6 months)