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Virtual program aims to stop intimate partner violence in young parents

NCT ID NCT07226401

Prevention Sponsor: RTI International 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a 10-session online program called Safe Dates for Young Parents can help prevent intimate partner violence among teens who are pregnant or parenting. About 80 participants aged 16-21 will be randomly assigned to either this program or a general health education program. Researchers will track attendance, engagement, and whether participants report fewer experiences of physical or psychological violence from a partner up to 6 months later.

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 80 people

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

Started

Nov 2025

Expected to finish

Jul 2026

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

16 to 21 years

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: Pregnant or parenting youth (Pilot RCT participants) * Aged 16-21 years. * Currently pregnant, partner of a pregnant person, or parenting a child (i.e., have contact with child at least once per week). * Able to speak and read English. * Willing and able to provide written informed consent. * Willing and able to provide adequate contact/locator information. Facilitators (IDI participants) * Aged 18 years or older. * Trained and served as a facilitator of the virtual SDYP intervention. * Able to speak and read English. * Able and willing to provide verbal informed consent. Exclusion Criteria (Pilot RCT participants): * Has any other condition that, in the opinion of the PI or their designee, would preclude informed consent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives. * Currently participating or will be participating in a violence prevention education program in the next 3 months. * Previously participated in the Empowering Young Parents study.

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As listed by the trial registrant

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

Gender-based violence Intimate partner violence

How to take part

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

  1. The places running it

    1 site. 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

  • RTI International

    RECRUITING

    Durham, North Carolina, 27713, United States

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