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NCT05579990Completed

Feasibility of Meal Delivery Postpartum

Feasibility of a Meal Delivery Intervention for Postpartum Weight Management

Source: ClinicalTrials.gov · Last updated 23 Sept 2025

Brief summary (registry, in English)

This study is being done to assess the feasibility and acceptability of a meal delivery intervention among low-income postpartum women with obesity.

Status (registry)
Completed
Study type
Interventional
Enrollment
11 (actual)
First submitted
11 Oct 2022
Start date
27 Sept 2023
Primary completion date
29 Jul 2024
Lead sponsor
University of Alabama at Birmingham
Diseases
Obesity
NCT number
NCT05579990

What you commit to

  • Study type: Interventional
  • Participants enrolled: 11
  • From 27 Sept 2023 to the primary completion date, 29 Jul 2024
  • 1 site 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

  • Current use of medication expected to significantly impact body weight

Other illness

  • 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)

Other

  • Self-reported diagnosis of anorexia or bulimia
  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alabama at Birmingham
Coordinator of this site? Confirm its status
BirminghamUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.