CHIME: Comparing Health Interventions for Maternal Equity
Stanford University · with Patient-Centered Outcomes Research Institute · NCT06724172
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 795
- US sites recruiting
- 3
- Study start
- January 22, 2026
- Record last updated
- March 5, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this comparative effectiveness trial is to compare how three different approaches to overcome barriers to resources and provide nutrition and physical activity counseling improve maternal healthy weight in pregnancy and postpartum.
The main question it aims to answer is which of the two multi-level, multi-component interventions has greater effectiveness in reducing maternal postpartum weight retention at 12-months postpartum.
Hypothesis (primary): Both multi-level, multi-component interventions will have greater effectiveness reducing maternal postpartum weight retention at 12-months postpartum than the usual care group.
Hypothesis (secondary): The community-based intervention will have greater effectiveness than the self-management intervention.
Participants will be asked to participate in one of the study interventions from early pregnancy until 12 months postpartum and complete five research visits. General procedures include completion of:
- Questionnaires
- Dietary recalls
- In-depth interviews
- Anthropometric measurements
- Collection of blood via finger stick or blood panel
Being studied: Self-Management; Community-Based
Conditions: Obesity and Overweight; Nutrition; Chronic Disease; Diabetes; Pregnancy
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Maternal age 18 years or older
- Maternal gestational age ≤ 20 weeks with viable singleton pregnancy documented on first trimester ultrasound with an intention to continue pregnancy to term
- Plans to continue receiving antenatal care at the recruitment site/network
- Maternal characteristics include at least one of the following:
- Self identifies as Black/African American
- Self identifies as Hispanic/Latino/a/e/x
- Insured by Medicaid
- Maternal ability to speak English or Spanish
- Completion of baseline data collection (maternal survey data, weight, and height measurement prior to randomization)
Exclusion Criteria
- Age \< 18 years at baseline because of unique developmental differences of adolescents and regulations regarding age of consent
- Underweight (BMI \<18 kg/m2) at pre-pregnancy period
- Underlying disease/treatment that might impact weight status (e.g., significant gastrointestinal conditions, major psychiatric disorders, and others at the discretion of the study clinician)
- Unwillingness or inability to complete study visits or intervention components
- Unwillingness or inability to commit to intervention components for self or infant, including plans to move more than 100-mile radius from recruitment site
- Multiple gestations
Recruiting US locations
New York Presbyterian Queens
Flushing, NY 11355
Site contact: Research Coordinator · 718-670-1707 · rjv9007@nyp.org
Columbia University Medical Center
New York, NY 10012
Site contact: Maxine Ashby-Thompson, EdD, MPH · 212-342-2969 · ma453@cumc.columbia.edu
NYU Langone Health
New York, NY 10016
Site contact: Tanisha Green · (646) 501-3868 · tanisha.green@nyulangone.org
Study contacts (from the official record)
- Jennifer Woo Baidal Associate Professor, MD, MPH · 650-721-2250 · jwoo1@stanford.edu
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