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Meal Delivery for Postpartum Weight Management
N/A
Recruiting
Led By Camille S Worthington, PhD
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up three 24-hour dietary recalls on non-consecutive days at baseline (5-19 weeks postpartum) and follow-up (14-29 weeks postpartum)
Awards & highlights
Study Summary
This trial aims to help low-income postpartum women with obesity get healthy meals delivered to their door.
Who is the study for?
This trial is for low-income postpartum women with obesity who are 18 or older, have had a healthy single baby recently, and live where meal delivery is available. They should not be on weight-impacting meds, involved in other diet studies, or have severe mental health issues.Check my eligibility
What is being tested?
The study tests if delivering meals to new moms with obesity is practical and well-received. It's focused on those who've just given birth and meet specific income criteria.See study design
What are the potential side effects?
Since this trial involves meal delivery without medical interventions, there aren't typical side effects like you'd see with drugs; however, dietary changes may affect digestion or food sensitivities.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ three 24-hour dietary recalls on non-consecutive days at baseline (5-19 weeks postpartum) and follow-up (14-29 weeks postpartum)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~three 24-hour dietary recalls on non-consecutive days at baseline (5-19 weeks postpartum) and follow-up (14-29 weeks postpartum)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Participant Adherence to Intervention
Secondary outcome measures
Change in Participant Satisfaction with Diet
Participant Retention
Study Participation Rate
Other outcome measures
Change in Food Security
Change in Healthy Eating Index score from baseline to follow-up
Change in Healthy Eating Self-Efficacy
+3 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Meal DeliveryExperimental Treatment1 Intervention
Meal delivery intervention program designed to help low income postpartum women lose weight through weekly meal delivery and behavioral strategies.
Find a Location
Who is running the clinical trial?
University of Alabama at BirminghamLead Sponsor
1,594 Previous Clinical Trials
2,282,459 Total Patients Enrolled
72 Trials studying Obesity
474,258 Patients Enrolled for Obesity
Camille S Worthington, PhDPrincipal InvestigatorUniversity of Alabama at Birmingham
1 Previous Clinical Trials
18 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am 18 years old or older.I have been diagnosed with anorexia or bulimia.I have a major health condition like kidney disease, cancer, or diabetes.I am taking medication that can greatly affect my weight.I cannot or will not eat the meals provided by the study.I gave birth 5 to 18 weeks ago.I am receiving treatment for a severe psychiatric disorder.
Research Study Groups:
This trial has the following groups:- Group 1: Meal Delivery
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Obesity Patient Testimony for trial: Trial Name: NCT05579990 — N/A
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