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Empowering Young Parents: Building Healthy Relationships Study (EYP)

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RTI International

Status

Enrolling

Conditions

Gender-based Violence
Intimate Partner Violence

Treatments

Behavioral: Safe Dates for Young Parents (SDYP)

Study type

Interventional

Funder types

Other

Identifiers

NCT06576193
TP2AH000082

Details and patient eligibility

About

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?
  • Will the SDYP intervention have any effect on the prevention or reduction of intimate partner violence (IPV)?
  • Will the SDYP intervention have any effect on the attitudes and beliefs about healthy relationships?

Researchers will compare the behaviors, attitudes, and beliefs about sexual and reproductive health and relationships of participants assigned to the SDYP intervention group to participants assigned to the control (non-SDYP intervention) group to see if there is any difference or changes in those behaviors, attitudes, and beliefs before-and-after or without the SDYP intervention.

Participants in the SDYP intervention will attend ten (10) 50-minute group sessions that will involve interactive discussions, thinking through life-like scenarios, games, role-plays, brainstorming, and a poster contest and theatrical play.

Enrollment

600 estimated patients

Sex

Female

Ages

14 to 21 years old

Volunteers

Accepts Healthy Volunteers

Inclusion 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.

Exclusion criteria

  • 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 participation should the participant be randomized to the SDYP 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 otherwise interfere with achieving the study objectives.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

600 participants in 2 patient groups

Safe Dates for Young Parents (SDYP)
Experimental group
Description:
Participants will receive and complete SDYP intervention activities focused on healthy relationships and intimate partner violence (IPV) prevention plus standard services offered at the study site.
Treatment:
Behavioral: Safe Dates for Young Parents (SDYP)
Standard Services Only
No Intervention group
Description:
Participants will only receive standard-of-care programming that typically includes services such as one-on-one strength-based case management and comprehensive sex education. The standard services will not address IPV or healthy relationships content that composes the SDYP intervention. Referrals to additional services will be offered to all participants, as needed.

Trial contacts and locations

6

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Central trial contact

Marni Kan, PhD

Data sourced from clinicaltrials.gov

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