Mobile App Logging for Diabetes in Pregnancy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-100
SponsorCarolyn Zahler-Miller
About this trial
To determine the effect of using a mobile app versus paper logs on compliance and percentage in range blood sugars in monitoring blood sugar in pregnant women with diabetes.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
18 years and older
Verified intrauterine pregnancy
At least 12 weeks gestation
Diagnosed with either type 2 diabetes mellitus or gestational diabetes mellitus.
Disqualifiers
Patients with less than 4 weeks anticipated to be remaining in pregnancy
Pre-existing use of a continuous glucose monitor or other mobile application for glucose tracking
Type 1 diabetes mellitus
Non-English speaking patients
Trial design
Design model
Parallel
Treatments tested in this trial
OneTouch Reveal application
BehavioralEvaluate if compliance with glucose logging and percentage of in range glucoses changes with use of a mobile application instead of paper logging
Treatment groups
40 Participants
are divided into 2 treatment groupsGroup A: Mobile App armExperimental treatment 1 intervention
Group B: Paper Log ArmNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Compliance
percentage of actual blood glucose values logged compared to expected.
Time frame
4 weeksSecondary outcomes
1
Percentage of in-range blood glucose levels
Percentage of blood glucose levels in pregnancy appropriate range out of total blood glucose levels logged.
Time frame
4 weeksSponsors and contacts
Click on the lead sponsor to view all of their trials.
Carolyn Zahler-Miller
Lead sponsor
Augusta University
Sponsor institution
Source ClinicalTrials.gov