NCT03301792Active, not recruiting
Group Versus Traditional Prenatal Care for Diabetes
Group Versus Traditional Prenatal Care for Diabetes: A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 21 Aug 2026
Brief summary (registry, in English)
The investigators primary objective is to conduct a randomized trial to determine the effect of diabetes group prenatal care on glycemic control and postpartum weight retention in women with type 2 diabetes and gestational diabetes.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 117 (estimated)
- First submitted
- 15 Sept 2017
- Start date
- 14 Sept 2017
- Primary completion date
- 17 Nov 2025
- Lead sponsor
- Washington University School of Medicine
- Diseases
- Type 2 diabetes
- NCT number
- NCT03301792
What you commit to
- Study type: Interventional
- Planned participants: 117
- From 14 Sept 2017 to the primary completion date, 17 Nov 2025
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior participation in diabetes group care
Other illness
- Type 1 Diabetes
- Serious psychiatric illness including schizophrenia necessitating more care than can safely be provided in group setting, as deemed by medical provider.
Other
- Multiple gestation
- Major fetal anomaly
- Serious medical co-morbidity necessitating more care than can be safely provided in group setting, as deemed by medical provider.
Who the study is looking for
- English speaking
- Type 2 diabetes OR gestational diabetes diagnosed by 2-step method(1) OR likely pre-existing Type 2 diabetes with one of the following during pregnancy and \</= 34 weeks:
- 1 hour glucose challenge test \>/= 185mg/dL OR
- A1c \>/= 6.5% OR
- Fasting plasma glucose \> 126mg/dL (2)
- Ability to attend group prenatal visit at specified days and times
- Willingness to be randomized at 22 weeks 0 days-34 weeks 0 days OR initial visit between 24 weeks 0 days-34 weeks 0 days
- Ability to give informed consent
Age in the registry: 18 years to 50 years · Sex: Female · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Utah Coordinator of this site? Confirm its status | Salt Lake City | United States | Unknown status |
| Washington University in St. Louis Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.