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Empowerment program for pregnant moms shows promise in reducing trauma and boosting Baby's health

NCT ID NCT04068662

Symptom relief Sponsor: University of Notre Dame 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a program called the Pregnant Moms' Empowerment Program (PMEP) for pregnant women who had experienced intimate partner violence in the past year. The goal was to see if the program could improve mothers' mental health, reduce the chance of further violence, and help their babies develop well. About 230 women took part, either in the PMEP or a general support group, and were followed for over a year after giving birth.

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

424 people

The number who actually took part.

Started

Jul 2019

Finished

Nov 2025

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

3 months to 55 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: * currently pregnant (primi or multiparous) * experienced intimate partner violence within the past year * English speaking * age 16 or older * between 10-30 weeks pregnant Exclusion Criteria: * fails to meet inclusion criteria * unavailable or unwilling to participate in core study components, including groups

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Conditions

The condition(s) this trial relates to.

Infant Behavior post-traumatic stress disorder postpartum depression

As listed by the trial registrant

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

Infant behavior Parenting Postpartum depression Posttraumatic stress disorder Violence

Contacts and locations

Locations

  • University of Memphis

    Memphis, Tennessee, 38152, United States

  • University of Notre Dame

    Notre Dame, Indiana, 46556, United States

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