Heart health check: new study tests postpartum program to cut cardiovascular risk
NCT ID NCT07420465
First seen Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study follows 200 pregnant women in Ghana from their third trimester through six months after birth. It measures blood pressure and artery stiffness to see if a structured education program on heart health, nutrition, and stress management can reduce long-term cardiovascular risk. The goal is to develop a scalable screening and intervention strategy for new mothers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Postpartum Cardiovascular Disease (CVD) Risk Reduction Program (behavioral intervention)
- What this could lead to
- If successful, this could lead to a simple, scalable program to help new mothers lower their heart disease risk after pregnancy.
- What could go wrong
- This is an early-stage study with no phase, so results are preliminary. The program may not show significant improvements in blood pressure or arterial stiffness, and findings from Ghana may not apply to other populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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School of Public Health
RECRUITINGAccra, Ghana
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