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Sugar Text: A Randomized Controlled Trial of a Text Message Intervention for Women With Diabetes in Pregnancy

Sugar Text: A Randomized Controlled Trial of a Text Message Intervention for Women With Diabetes in Pregnancy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01973374
Acronym
Sugar Text
Enrollment
30
Registered
2013-10-31
Start date
2013-01-31
Completion date
2014-04-30
Last updated
2015-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes in Pregnancy, Gestational Diabetes, Texting Interventions

Brief summary

Maternal diabetes in pregnancy can negatively impact fetal well-being and contribute to adverse pregnancy outcomes. Much of the morbidity associated with diabetes in pregnancy can be minimized with tight glucose control. A number of studies in non-pregnant populations have highlighted the feasibility, acceptability and efficacy of text messaging interventions for improving diabetic compliance and control. This study will investigate whether a text messaging intervention is feasible and effective in an urban, diabetic, obstetric clinic and whether this intervention can improve compliance with diabetes care, glucose control and pregnancy outcomes. The study will also assess satisfaction with the intervention itself.

Interventions

Sponsors

University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Pregnant women aged 18-50 years * Planned delivery at Hospital of the University of Pennsylvania

Exclusion criteria

* Gestational age greater than 34 weeks at initial visit in the Penn Perinatal Diabetes Program * Women who are unable to read English as all text messages will be in English * Women who do not have a cellular phone capable of receiving text messages as this is the study intervention

Design outcomes

Primary

MeasureTime frameDescription
Patient Satisfactiondate of enrollment up to 12 weeks post partumPatient satisfaction with the texting intervention as measured by a post-study survey
Compliance with Obstetric and Diabetes CareOB screening visit through 12 weeks postpartumProportion of prenatal visits attended, proportion of assigned blood glucose logs sent to clinic for review, proportion of assigned blood glucose values checked, compliance with attendance at postpartum visit.

Secondary

MeasureTime frameDescription
Efficacy measuresDiabetes diagnosis through 12 weeks postpartumMeasuring the proportion of blood glucose values within the target range each week; mean fasting and postprandial blood glucose values measured weekly; change in hemoglobin A1C (for pregestational diabetics) from initiation of care to the third trimester
Healthcare Utilization MeasuresScreening OB visit through 12 weeks postpartumMeasuring the number of visits to the perinatal evaluation center related to diabetes care and the total number of antepartum hospitalizations.
Maternal OutcomesDelivery date through 12 weeks postpartumMeasuring the mode of delivery (spontaneous vaginal, operative vaginal, cesarean section), complications of delivery (shoulder dystocia, postpartum hemorrhage, third and fourth degree lacerations), and length of hospital stay.
Neonatal OutcomesNeonate delivery through 12 weeks postpartumMeasuring fetal demise; neonatal death; birthweight; large for gestational age; small for gestational age; APGAR scores; umbilical cord blood gas; NICU admission; respiratory distress; hypoglycemia; hyperbilirubinemia; length of hospital stay

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026