NCT05619705Recruiting
Healthy for Two-Home Visiting (H42-HV): Health Coaching for Pregnant Women
Effectiveness of Health Coaching to Reduce Cardiometabolic Risk in Early Home Visiting Services
Source: ClinicalTrials.gov · Last updated 8 Jun 2026
Brief summary (registry, in English)
The purpose of this study is to compare the effectiveness of H42-HV integrated into home visiting compared with usual home visiting services in reducing postpartum weight retention (difference between pre-pregnancy weight and weight at 6 months postpartum) among pregnant and postpartum participants. The overall goal is to improve long-term cardiometabolic health.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 360 (estimated)
- First submitted
- 9 Nov 2022
- Start date
- 25 Apr 2023
- Primary completion date
- 15 Dec 2026
- Lead sponsor
- Johns Hopkins University
- Diseases
- Obesity
- NCT number
- NCT05619705
What you commit to
- Study type: Interventional
- Planned participants: 360
- From 25 Apr 2023 to the primary completion date, 15 Dec 2026
- 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
- Type 1 diabetes or taking insulin prior to delivery
Other illness
- Active substance abuse disorder (except marijuana)
- Psychiatric or substance use related hospitalization in past 1 year
- Active eating disorder
Other
- 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
Who the study is looking for
- 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)
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Johns Hopkins School of Nursing Coordinator of this site? Confirm its status | Baltimore | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.