Postpartum Cardiovascular Care After Pregnancy
Official title: Cardiometabolic Risk in Pregnancy and Postpartum
Run by University of North Carolina, Greensboro · NCT07420465 · Data updated 2026-11-12
This study tests whether a postpartum education program can improve blood pressure and early heart‑health markers in women in their third trimester to six months after giving birth in Accra, Ghana.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 45 Years |
| Sex | Women only |
| Enrollment | 200 (estimated) |
| Sponsor | University of North Carolina, Greensboro Academic / other |
| Locations | 1 site (Accra) |
| Status | Recruiting |
| Started | April 1, 2026 |
| Main results expected | June 28, 2027 |
| Study ends | December 2027 |
| Registry record updated | July 16, 2026 |
| Trial ID | NCT07420465 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are women aged 18+ in the third trimester, living in Accra, with singleton pregnancies, who may or may not have gestational hypertension, preeclampsia, or gestational diabetes.
✕Probably not a fit
Women with preexisting cardiovascular disease or diabetes prior to pregnancy may not benefit from the postpartum-focused interventions as studied.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial will enroll pregnant women 18 years or older, in their third trimester, and follow them through six months postpartum to measure blood pressure changes and early cardiovascular risk markers. Participants may have pregnancy-related cardiometabolic issues or be without them. The study compares a postpartum cardiovascular risk reduction program and enhanced postpartum care to standard approaches to see if risk monitoring and outcomes improve. Data from this study will help shape scalable screening and intervention strategies for long-term cardiovascular health in women after pregnancy.
Why it matters
Potential benefit: If successful, the program could lead to better blood pressure control and earlier detection of cardiovascular risk in postpartum women.
How similar studies have gone: Prior research in related postpartum care has shown potential benefits for cardiovascular monitoring and risk reduction in similar populations, though this exact approach is novel in this geographic setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Singleton pregnancy * 18 years and older * 3rd trimester of pregnancy at enrollment * Will be living in the area for the study duration * Women with or without pregnancy complications (e.g., gestational hypertension, preeclampsia, gestational diabetes) Exclusion Criteria: * Multiple births * Diagnosed CVD or diabetes prior to pregnancy * Renal or other serious maternal diseases pre-pregnancy
Where it's running
-
School of Public Health
Accra, Ghana Recruiting
Study contacts
- Study coordinator: Forgive Avorgbedor, PhD
- Email: f-avorgbedo@uncg.edu
- Phone: 336-334-5111
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.