Cure My Disease

Don't miss your cure!

 Log in / Sign up

Can home visits after childbirth save lives in rural mississippi?

NCT ID NCT07006324

Disease control Sponsor: Jackson State University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study tests a community-based home visiting program for high-risk postpartum women in five rural Mississippi counties. The program uses the PEN-3 model to build trust and connect mothers with healthcare. Researchers will measure whether the program reduces emergency room visits and severe complications, especially among Black women.

What this could mean

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

Active substance
home visiting program based on the PEN-3 behavioral model
What this could lead to
If it works, this program could reduce emergency room visits and severe complications after childbirth for high-risk women in underserved rural areas.
What could go wrong
This is a behavioral intervention study, not a drug trial, so results may vary by community. It is also limited to five counties in Mississippi, so findings may not apply elsewhere.

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

About 500 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2025

Expected to finish

Jun 2030

An estimate. End dates often move.

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 to 45 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Identified as high risk pregnancy * Postpartum mothers/parents 18-45 years * Resident of the one of 5 target counties (Washington, Bolivar, Scott, Humphreys, and Carroll) Exclusion Criteria: * not identified as high risk pregnancy * 18 years of age postpartum * cesarean birth * non-resident of the 5 target counties

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Maternal behavior are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Conditions

The condition(s) this trial relates to.

postpartum depression

As listed by the trial registrant

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

Maternal behavior Postpartum mood disturbance

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Mississippi State Department of Health

    RECRUITING

    Jackson, Mississippi, 39216, United States

  • University of Mississippi Medical Center

    RECRUITING

    Jackson, Mississippi, 39216, United States

More trials for these conditions

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