Gestational Diabetes Clinical Trial
Official title:
Meals 4 Moms: Development and Feasibility of a Multilevel Community-based Lifestyle Intervention for Gestational Diabetes
The goal of the project is to conduct a pilot feasibility randomized trial comparing a community-based lifestyle intervention called Meals for Moms (M4M) versus the usual care for pregnant persons diagnosed with gestational diabetes (GDM). Participants will be randomly placed into the usual care (UC) comparison group or the M4M healthy living program, which includes continued GDM education, physical activity level monitoring, and delivery of medically-tailored GDM meals. The trial will assess if M4M is feasible for the management of gestational diabetes in pregnant patients.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | September 30, 2024 |
Est. primary completion date | September 30, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 49 Years |
Eligibility | 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 time of diagnosis at time of enrollment. - Currently receiving gestational diabetes management at the UConn Health Maternal Fetal Clinic, St. Francis's Hospital Women's Health clinic, Hartford Healthcare Women's Ambulatory 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/desktop computer that they can use to participate in the study - Medical clearance to participate from prenatal care provider including clearance to engage in physical activity - Able to provide verbal or written consent for each component of the study procedures and data collection - Currently lives within one of the meal delivery areas in Connecticut to allow for meal delivery (total of 32 eligible towns/cities) 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., placenta accreta, prior classical incision) at time of eligibility screening or at any time prior to randomization. - Concurrent participation in another research study providing intervention related to GDM, 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 care provider 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 expected pregnancy due date. |
Country | Name | City | State |
---|---|---|---|
United States | UConn Health | Farmington | Connecticut |
Lead Sponsor | Collaborator |
---|---|
UConn Health | Hartford Hospital, Trinity Health Of New England, University of Connecticut |
United States,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Acceptability (participate again) | Percent of participants who report they would be likely or very likely to participate again if they had gestational diabetes (GDM) again. | Follow-Up (within 2 weeks post-delivery) | |
Primary | Acceptability (recommended) | Percent of participants who report they would be likely to very likely to recommend the M4M intervention to a friend with gestational diabetes (GDM). | Follow-Up (within 2 weeks post-delivery) | |
Primary | Recruitment | Recruitment rates will be calculated from the number of patients approached and reasons for ineligibility and non-participation. | Baseline | |
Primary | Retention | Proportion of participants who complete any aspect of the follow-up assessment. | Follow-Up (within 2 weeks post-delivery) | |
Primary | Receipt of intervention (Meal Ordering) | Percent of participants who spent at least 80% of weekly $260 food budget. | Follow-Up (within 2 weeks post-delivery) | |
Primary | Receipt of intervention (Exercise Session Completion) | Percent of participants who completed at least 80% of exercise sessions they were eligible to complete. | Follow-Up (within 2 weeks post-delivery) |
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