Feasibility of Meal Delivery Postpartum (NCT05579990) | Clinical Trial Compass
CompletedNot Applicable
Feasibility of Meal Delivery Postpartum
United States11 participantsStarted 2023-09-27
Plain-language summary
This study is being done to assess the feasibility and acceptability of a meal delivery intervention among low-income postpartum women with obesity.
Who can participate
Age range18 Years
SexFEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Medicaid eligible and/or have a household income at or below 185 percent of the federal poverty line
* 18 years of age or older
* Initiated prenatal care at a University of Alabama at Birmingham prenatal clinic
* Experienced a healthy singleton pregnancy
* 5-45 weeks postpartum at enrollment
* Body mass index \>= 30 at enrollment
* Residing within the meal company's delivery radius
* Willing to consent
Exclusion Criteria:
* Self-reported major health condition (such as renal disease, cancer, or Type 1 or Type 2 diabetes)
* Current treatment for severe psychiatric disorder (such as schizophrenia)
* Self-reported diagnosis of anorexia or bulimia
* Current use of medication expected to significantly impact body weight
* Current substance abuse
* Participation in another dietary and/or weight management intervention postpartum
* Unable to understand and communicate in English
* Unwilling or unable to consume study meals
What they're measuring
1
Self-Reported Proportion of Received Study Meals Consumed
Timeframe: Collected weekly from intervention start (6-45 weeks postpartum) to follow-up (14-53 weeks postpartum)