Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Health coaching for pregnant women to reduce postpartum weight retention

Official title: Effectiveness of Health Coaching to Reduce Cardiometabolic Risk in Early Home Visiting Services

Run by Johns Hopkins University · NCT05619705 · Data updated 2026-11-12

This study is testing a health coaching program for Black and Latinx pregnant women to see if it helps them keep off extra weight after having a baby.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment360 (estimated)
SponsorJohns Hopkins University
Academic / other
Locations1 site (Baltimore, Maryland)
StatusRecruiting
StartedApril 25, 2023
Main results expectedDecember 15, 2026
Study endsDecember 15, 2026
Registry record updatedJune 8, 2026
Trial IDNCT05619705 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are pregnant individuals who are less than or equal to 33 weeks gestation with a pre-pregnancy BMI of 25.0 kg/m² or higher.

Probably not a fit

Patients with type 1 diabetes, multiple pregnancies, or significant mobility issues may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study compares the effectiveness of the Healthy for Two-Home Visiting (H42-HV) program, which integrates health coaching into home visiting services, against usual home visiting services. The intervention is specifically designed for Black and Latinx pregnant and postpartum individuals and aims to reduce postpartum weight retention by promoting healthier behaviors. Participants will receive health coaching calls, access to a web-based app for goal setting, and tools for tracking health behaviors and self-weighing. The program emphasizes culturally adapted learning activities to ensure accessibility and engagement.

Why it matters

Potential benefit: If successful, this intervention could significantly reduce postpartum weight retention and improve overall health outcomes for pregnant and postpartum individuals.

How similar studies have gone: Other studies have shown success with similar behavioral interventions aimed at reducing postpartum weight retention, indicating potential for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Pregnant, ≤33 weeks gestation
* Singleton pregnancy
* Pre pregnancy BMI≥25.0 Kg/m\^2 (calculated based on self-reported pre pregnancy height and weight)
* Able to provide informed consent
* English or Spanish speaking
* Completion of screening and baseline data collection
* Willing to participate in the intervention and data collection procedure (e.g., home weights)

Exclusion Criteria:

* Type 1 diabetes or taking insulin prior to delivery
* Pregnant with multiple fetuses
* Unable to walk 1 block without pain or shortness of breath
* Not cleared by the study's clinicians or home visiting program staff
* Planning to relocate from area during next 1 year
* Active substance abuse disorder (except marijuana)
* Psychiatric or substance use related hospitalization in past 1 year
* Active eating disorder

Where it's running

  • Johns Hopkins School of Nursing
    Baltimore, Maryland, United States
    Recruiting

Study contacts

  • Principal investigator: Kelly Bower, PhD, MSN/MPH — Johns Hopkins School of Nursing
  • Study coordinator: Kelly M Bower, PhD, MSN/MPH
  • Email: kbower1@jhu.edu
  • Phone: 410-955-4280

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.