Actively Recruiting
Bridges to Primary Care: Transforming Postpartum Primary Care Coordination for People With Chronic Conditions
Led by Massachusetts General Hospital · Updated on 2025-06-03
1320
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
M
Massachusetts General Hospital
Lead Sponsor
H
Harvard School of Public Health (HSPH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Many pregnant people have chronic medical conditions or pregnancy-related health issues that increase their risk for long-term disease. Despite being closely followed during pregnancy, many experience a drop in healthcare support after delivery, missing important primary care visits. This trial aims to improve postpartum primary care engagement, quality, and patient experience by using a behavioral economics-based program integrated into usual inpatient postpartum care. The goal is to make primary care coordination a standard part of postpartum care and promote ongoing health management. The study compares routine postpartum care with an intervention that schedules primary care visits by default, sends tailored reminder messages to patients, provides ongoing care recommendations to their primary care clinicians, and gives patients a summary of care suggestions after pregnancy. This randomized controlled trial will include 1,320 participants and assess outcomes at multiple time points after delivery. Participants will be followed through surveys and medical records to assess completion of primary care visits, use of recommended screenings and counseling, patient-reported mental health, and primary care engagement over time. The study will monitor these outcomes at 155, 365, and 548 days after delivery to understand the intervention's impact on care continuity and patient experience. The trial aims to provide evidence to improve postpartum care for people with chronic conditions.
CONDITIONS
Brief Title
Facilitated Transitions From Postpartum to Primary Care Coordination for People With Chronic Conditions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Receiving obstetric care at an MGH-affiliated obstetrics practice (except MGH HOPE Clinic)
- Pregnant with a live fetus or delivered a live-born baby at 24 weeks gestation or later
- If postpartum, has a living neonate at enrollment
- Has one or more of the following: chronic or essential hypertension, pregnancy-related hypertension (e.g., pre-eclampsia), type 1 or 2 diabetes, gestational diabetes, class II obesity (BMI 35 or higher), depression, or anxiety disorder
- Has a primary care clinician listed in medical records
- Has access to or agrees to use the electronic health record patient portal and consents to contact
- Can read and speak English or Spanish
- Is 18 years old or older
You will not qualify if you...
- Any individual not meeting all inclusion criteria
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Duration - Starts at delivery and continues during the postpartum period
Participants receive an intervention integrated into routine inpatient postpartum care, which includes default primary care provider visit scheduling, tailored nudge messages, ongoing care recommendations sent to the primary care provider, and a summary of recommendations after pregnancy given to the participant.
Visits occur as part of routine postpartum care with scheduled primary care provider visits
Duration - Up to 548 days (about 18 months) after delivery
Participants' engagement with primary care and health outcomes are monitored through 18 months after delivery to assess sustained primary care use, health screenings, counseling, and overall experience.
Participants may attend primary care visits and complete assessments at approximately 5 months, 12 months, and 18 months postpartum
Trial Site Locations
Total: 1 location
1
Massachusetts General Hospital
Boston, Massachusetts, United States, 02115
Actively Recruiting
Research Team
M
Mark A Clapp, MD, MPH
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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