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Life sciences · Interventional Study
ClinicalTrials.gov · September 22, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT06445530). This is a study registration, not published results. Lead sponsor: Johns Hopkins University. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 40 participants (ESTIMATED). Conditions: Obesity, Maternal, Gestational Diabetes. Interventions: BEHAVIORAL: MFeast ENHANCED; BEHAVIORAL: MFeast Usual Care. Primary outcome measures: Participant Enrollment Rate , 6-8 months postpartum; Participant Retention , 6-8 months postpartum; Adherence as assessed by self-reported food consumption scores and photographs sent to the study team via secure messaging app , 6-8 months postpartum; Satisfaction as assessed by focus groups and the 8 item Client Satisfaction Questionnaire- (CSQ-8) , 6-8 months postpartum; Participant Engagement assessed by frequency and quality of meal discussions , 1-6 months postpartum. Brief summary: The goal of this clinical trial is to better understand how different strategies, timing, and enhancements to medically tailored food delivery will address structural inequities in the food environment, empower communities to sustain behavior change, and ultimately improve postpartum weight control to prevent type 2 diabetes-a potent contributor to disparate mortality among Black women. The main aims of the study are: * To conduct a pilot randomized control trial to test the feasibility, acceptability, and effectiveness of a multi-component Medically Tailored Food (MTF) intervention, Moveable Feast ENHANCED (a hybrid MTF intervention with a patient-activated change from prepared meals to fresh food delivery, customized for postpartum people, culturally customized for engagement and adherence, and food provision for dependents) versus MFeast Usual Care (prepared medically tailored foods only) * To test sustainability and scalability. Participants will: * Respond to online surveys (supported by study team members via scheduled phone calls) via REDCap links shared before each study visit at baseline, 3, 6 months post-delivery after the baseline survey. * Submit anthropometric data (i.e, weight) and information about laboratory results ( e.g. HgbA1C)