Last updated: February 7, 2024
Sponsor: UConn Health
Overall Status: Active - Recruiting
Phase
N/A
Condition
Diabetes Prevention
Diabetes And Hypertension
Pregnancy Complications
Treatment
Meals4Moms Intervention
Clinical Study ID
NCT06227247
23-190SSF-2
Ages 18-49 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- 18-49 years old
- Current singleton pregnancy
- GDM diagnosis between 24+0 and 31+6 weeks gestation, and no more than 4weeks from timeof diagnosis at time of enrollment.
- Currently receiving gestational diabetes management at the UConn Health Maternal FetalClinic, St. Francis's Hospital Women's Health clinic, Hartford Healthcare Women'sAmbulatory Health Services (WAHS)
- Intends to deliver at either UConn Health, St. Francis Hospital or Hartford Healthcare
- Able to read and understand English well enough to participate in the study in English
- Daily access to the internet from smartphone, tablet computer, or laptop/desktopcomputer that they can use to participate in the study
- Medical clearance to participate from prenatal care provider including clearance toengage in physical activity
- Able to provide verbal or written consent for each component of the study proceduresand data collection
- Currently lives within one of the meal delivery areas in Connecticut to allow for mealdelivery (total of 32 eligible towns/cities)
Exclusion
Exclusion Criteria:
- Unable or unwilling to give informed consent or communicate with study staff.
- Diabetes mellitus (Type I or Type II).
- GDM diagnosed prior to 24 weeks gestation or after 32+0 weeks gestation.
- Patient is scheduled for a preterm delivery for medical reasons (i.e., placentaaccreta, prior classical incision) at time of eligibility screening or at any timeprior to randomization.
- Concurrent participation in another research study providing intervention related toGDM, pregnancy, diet, and/or physical activity.
- Medical conditions that may result in the inability to tolerate solid foods (i.e.,hyperemesis gravidarum).
- Medical condition which would prohibit participation as indicated by prenatal careprovider providing medical clearance.
- Dietary restrictions that cannot be accommodated for during meal preparation.
- Currently does not live in one of the towns listed within the meal delivery area.
- Has plans to move to out of the meal delivery area between enrollment and expectedpregnancy due date.
Study Design
Total Participants: 40
Treatment Group(s): 1
Primary Treatment: Meals4Moms Intervention
Phase:
Study Start date:
February 01, 2024
Estimated Completion Date:
September 30, 2024
Study Description
Connect with a study center
UConn Health
Farmington, Connecticut 06030
United StatesActive - Recruiting
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