Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
ID06724172

CHIME: Comparing Health Interventions for Maternal Equity to Reduce Postpartum Weight Retention

Led by Stanford University · Updated on 2026-03-05

795

Participants Needed

4

Research Sites

10 weeks

Total Duration

On this page

Sponsors

S

Stanford University

Lead Sponsor

P

Patient-Centered Outcomes Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating how three different strategies to overcome barriers to resources and provide nutrition and physical activity counseling affect healthy weight in pregnant and postpartum women. The study focuses on which of two multi-level, multi-component interventions is more effective in reducing maternal weight retention 12 months after giving birth. The trial also compares these interventions to usual care, aiming to understand their impact on maternal postpartum weight and related health outcomes. Participants are randomly assigned to one of three groups: a self-management intervention offering social needs supports like grocery and transportation help combined with self-directed behavior tools; a community-based intervention involving detailed social needs assessments, active referral assistance, and group and individual physical activity support; or usual care, which includes standard social needs screening and provider-based lifestyle counseling. The interventions start in early pregnancy and continue until 12 months postpartum. Throughout the study, participants complete five research visits that include questionnaires, dietary recalls, in-depth interviews, body measurements, and blood collection via finger stick or blood panels. Researchers monitor maternal postpartum weight retention as the primary outcome at 12 months postpartum, along with household social needs and perinatal health outcomes. The study includes ongoing assessments and supports to track progress and adherence over the intervention period.

CONDITIONS

Brief Title

CHIME: Comparing Health Interventions for Maternal Equity

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Maternal age 18 years or older
  • Maternal gestational age 20 weeks or less with viable singleton pregnancy confirmed by first trimester ultrasound
  • Plans to continue receiving antenatal care at the recruitment site or network
  • Self-identifies as Black/African American or Hispanic/Latino/a/e/x, or insured by Medicaid
  • Ability to speak English or Spanish
  • Completion of baseline data collection including survey, weight, and height before randomization
Not Eligible

You will not qualify if you...

  • Younger than 18 years at baseline
  • Underweight before pregnancy (BMI less than 18 kg/m2)
  • Underlying diseases or treatments affecting weight status (such as major gastrointestinal or psychiatric conditions)
  • Unwilling or unable to complete study visits or intervention components
  • Unwilling or unable to commit to intervention for self or infant, including plans to move more than 100 miles from recruitment site
  • Multiple pregnancies (twins or more)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - From enrollment to 12 months postpartum

Participants receive either a self-management intervention through mobile health technology and/or mailings, a community-based intervention with social needs referrals and health coaching, or usual care involving social needs screening and provider-based lifestyle counseling.

Regular visits as scheduled by the study

Trial Site Locations

Total: 4 locations

1

Stanford University

Palo Alto, California, United States, 94304

Active, Not Recruiting

2

New York Presbyterian Queens

Flushing, New York, United States, 11355

Actively Recruiting

3

Columbia University Medical Center

New York, New York, United States, 10012

Actively Recruiting

4

NYU Langone Health

New York, New York, United States, 10016

Actively Recruiting

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Research Team

J

Jennifer Woo Baidal Associate Professor, MD, MPH

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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