New treatment option for Gender-based Violence
Official title Virtual Village for Young Parents
ClinicalTrials.gov ID: NCT07226401
What this study is testing
- What it's testing
- This project will study virtual delivery of Safe Dates for Young Parents (SDYP), a 10-session, group-based intimate partner violence (IPV) prevention program tailored for adolescents and young adults who are pregnant or parenting. This program has the potential to improve the health and well-being of young parents and their children, and virtual delivery may improve participants' ability to attend.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 16 to 21. Healthy volunteers may be eligible.
You may be able to join if
- 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.
You likely can't join if
- (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...
- 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.
See the full eligibility 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.
- (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...
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Durham, North Carolina, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 16 years to 21 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Durham, North Carolina, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.