Can better provider training save black and hispanic mothers?
NCT ID NCT07025057
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This study tests a training program for healthcare providers in Michigan to improve how they communicate with and care for Black and Hispanic pregnant individuals. The goal is to increase provider confidence and awareness of community resources, which may help reduce racial disparities in pregnancy-related deaths and complications. Researchers will survey providers before and after training to measure changes in knowledge and behavior.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Provider training on communication and cultural relevance
- What this could lead to
- If successful, this training could improve provider confidence and reduce racial disparities in pregnancy-related deaths and complications.
- What could go wrong
- This is a small, early-stage study measuring provider confidence, not direct health outcomes. It may not lead to lasting changes or reduce mortality.
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 480 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Aug 2030
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 years and older
- Sex
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Anyone
- 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: * Providing care to pregnant and postpartum women in Wayne, Kent, and Genesee Counties in MI Exclusion Criteria: * None
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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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Strong Beginings
RECRUITINGGrand Rapids, Michigan, 49503, United States
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