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New treatment option for Gender-based Violence
Official title Empowering Young Parents: Building Healthy Relationships Study
ClinicalTrials.gov ID: NCT06576193
What this study is testing
- What it's testing
- The goal of this trial is to learn how the Safe Dates for Young Parents (SDYP) intervention affects the sexual and reproductive health behaviors, and quality of, and attitudes surrounding intimate partner relationships in adolescents and young adults (AYA) assigned female sex at birth who are pregnant or parenting. The main questions it aims to answer are: Will the SDYP intervention have any effect on the sexual and reproductive health behaviors during the study period?
- 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 14 to 21, women only. Healthy volunteers may be eligible.
You may be able to join if
- Adolescent and Young Adult (AYA) [EYP study participants]
- Aged 14-21 years (inclusive) at Screening.
- Assigned female sex at birth.
- Currently pregnant or parenting their child who lives with them at least part-time.
- Able to speak and read English or Spanish.
You likely can't join if
- Per participant report at Screening or Enrollment, intends to travel away from their geographic area of residence for a time period that would...
- Has any other condition that, in the opinion of the Principal Investigator (PI) or their designee, would preclude informed consent, make study...
See the full eligibility criteria
- Adolescent and Young Adult (AYA) [EYP study participants]
- Aged 14-21 years (inclusive) at Screening.
- Assigned female sex at birth.
- Currently pregnant or parenting their child who lives with them at least part-time.
- Able to speak and read English or Spanish.
- Able and willing to provide verbal informed consent for enrollment in the EYP study.
- Able and willing to provide adequate contact/locator information.
- Able and willing to complete protocol requirements, including completion of three study interviews over one year. Study Facilitators (process evaluation participants)
- Aged 18 years or older.
- Trained and served as a facilitator of the SDYP intervention.
- Able to speak and read English.
- Able and willing to provide verbal informed consent.
- Per participant report at Screening or Enrollment, intends to travel away from their geographic area of residence for a time period that would interfere with study participation, including with intervention...
- Has any other condition that, in the opinion of the Principal Investigator (PI) or their designee, would preclude informed consent, make study participation unsafe, complicate interpretation of study outcome data, or...
The study team makes the final eligibility decision.
Where it's taking place
- Camden, Delaware, United States
- Georgetown, Delaware, United States
- Washington D.C., District of Columbia, United States
- Albany, Georgia, United States
- Atlanta, Georgia, United States
- Benton Harbor, Michigan, United States
- Charlotte, Michigan, United States
- Detroit, Michigan, United States
- Saginaw, Michigan, United States
- Graham, North Carolina, United States
- Hendersonville, North Carolina, United States
- Sanford, 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 female, 14 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 Camden, Delaware, United States; Georgetown, Delaware, United States; Washington D.C., District of Columbia, United States; Albany, Georgia, United States; Atlanta, Georgia, United States; Benton Harbor, Michigan, United States and 6 more location(s). 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.