The purpose of this study is to evaluate if in patients with gestational diabetes (GDM), adherence to postprandial glucose monitoring differs when performed 1-hour versus 2-hours after eating. The primary objective of this study is to evaluate difference in rate of adherence (binary outcome defined as \<80% or ≥80% of glucose log completed) between gestational diabetics who perform 1-hour versus 2-hour postprandial blood glucose testing.
Consented patients who are diagnosed with gestational diabetes will be randomized to either 1-hour or 2-hour postprandial blood glucose monitoring. A retrospective chart review from July 2020 until study commencement for patients from the same clinic will be used as a historical control group. This study will assess differences in adherence to testing.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Enrollment
140
Consented patients who are diagnosed with gestational diabetes will be randomized to 1-hour postprandial blood glucose monitoring.
Consented patients who are diagnosed with gestational diabetes will be randomized to 2 hour post prandial blood glucose monitoring
New York Prebyterian Hospital Weill Cornell
New York, New York, United States
Rate of adherence
Evaluate rate of adherence (binary outcome defined as \<80% or ≥80% of glucose log completed) between gestational diabetics who perform 1-hour versus 2-hour postprandial blood glucose testing.
Time frame: During the intervention
Percentage of postprandial glucose log complete, averaged over the duration of the study period
Time frame: During the intervention
Percentage of postprandial glucose log complete for each meal (breakfast, lunch, and dinner), averaged over the duration of the study period
Time frame: During the intervention
Percentage of elevated blood glucose values per week, averaged over the duration of the study period
Time frame: During the intervention
Number of patients who start insulin or oral hyperglycemic medication therapy prior to delivery.
Time frame: During the intervention
Gestational age at medication therapy initiation
Time frame: During the intervention
Timeframe from diagnosis of gestational diabetes to initiation of insulin therapy
Time frame: During the intervention
Number of subjects with a vaginal delivery
Time frame: At time of delivery
Number of subjects with an operative delivery
Time frame: At time of delivery
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Number of subjects with a caesarean section delivery
Time frame: At time of delivery
Number of subjects with a preeclampsia diagnosis
Time frame: During intervention
Neonatal birthweight
Time frame: At time of delivery
Number of subjects with shoulder dystocia
Time frame: At time of delivery
Number of patients with 3rd or 4th degree perineal lacerations
Time frame: At time of delivery
Number of patients with postpartum hemorrhage.
Time frame: At time of delivery
Number of stillbirths
Time frame: At time of delivery
Number of NICU admissions
Time frame: At time of delivery
Number of patients requiring supplemental oxygen support
Time frame: At time of delivery
Number of patients with diagnosis of hypoglycemia
Time frame: At time of delivery
Number of patients with diagnosis of hyperbilirubinemia
Time frame: At time of delivery
Number of patients with clavicular fracture
Time frame: At time of delivery
Number of patients with humeral fracture
Time frame: At time of delivery
Number of patients with brachial plexus palsy
Time frame: At time of delivery