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Community-Driven effort to improve postpartum health for black women

NCT ID NCT06689930

Knowledge-focused Sponsor: University of Wisconsin, Madison Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Sep 17, 2026 · Updated 3 times

Summary

This study aims to adapt a program called Staying Healthy After Childbirth (STAC) for Black women and birthing persons. Researchers will work with community organizations and advisory boards to identify barriers and facilitators to implementation. The goal is to make the program more acceptable and effective for this population.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to a culturally adapted program that improves postpartum health for Black women and birthing persons.
What could go wrong
This is a small, early-stage study focused on adaptation and feasibility, not testing health outcomes. Results may not apply broadly.

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

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

47 people

The number who actually took part.

Started

May 2025

Finished

Jul 2026

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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 (Interviews and Focus Groups): * Belong to the STAC-CAB or Lived Experience Group * Aged 18 or older Inclusion Criteria (CBO Staff): * Staff of CBO participating in PDSA cycle * Aged 18 years or older Inclusion Criteria (PDSA-Cycles): * Pregnant persons greater than or equal to 24 weeks gestation and prior to delivery or postpartum * Self-Identify as African American or Black * Aged 18 years or older * Capable of providing informed consent in English * Can follow M•care System use instructions in English * Have ownership of a functioning and reliable smartphone to upload and use the M•other App * Interested in preventing or managing blood pressure during pregnancy Exclusion Criteria (PDSA-Cycles): * Persistent second or third trimester bleeding at time of enrollment * Premature rupture of membranes in the current pregnancy at time of enrollment * Known unrepaired maternal congenital heart disease requiring surgical correction * Maternal heart failure * Chronic kidney disease specifically requiring dialysis * On greater than two antihypertensive medications at time of enrollment

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Conditions

The condition(s) this trial relates to.

hypertension, pregnancy-induced hypertensive disorder pregnancy disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Blood pressure Health equity Hypertension Pregnancy related

Contacts and locations

Locations

  • University of Wisconsin

    Madison, Wisconsin, 53792, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.