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Behavioural Intervention
Safe Dates Program for Intimate Partner Violence (EYP Trial)
N/A
Recruiting
Led By Alexandra Minnis, PhD
Research Sponsored by RTI International
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* Aged 18 years or older.
* Aged 14-21 years (inclusive) at Screening.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up month 12
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to see how a program called Safe Dates for Young Parents (SDYP) affects the behaviors and attitudes towards sexual health, relationships, and intimate partner violence in young females who are pregnant or
Who is the study for?
This trial is for young individuals assigned female at birth, aged 14-21, who are currently pregnant or parenting. They must be able to understand English or Spanish and provide informed consent. Participants should be willing to attend group sessions and complete study interviews over a year.
What is being tested?
The Safe Dates for Young Parents (SDYP) program is being tested to see if it can improve sexual/reproductive health behaviors and attitudes towards healthy relationships in adolescents/young adults facing gender-based violence. The study compares those receiving SDYP with a control group not receiving the intervention.
What are the potential side effects?
Since this trial involves educational interventions rather than medical treatments, traditional physical side effects are not applicable. However, participants may experience emotional discomfort when discussing sensitive topics like intimate partner violence.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
I am between 14 and 21 years old.
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I was assigned female at birth.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ three months, six months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~three months, six months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Condomless vaginal or anal sex (Month 12)
Secondary study objectives
Condomless vaginal or anal sex (Month 6)
Healthy relationship attitudes, beliefs, and behaviors
Intimate Partner Violence (IPV)
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Safe Dates for Young Parents (SDYP)Experimental Treatment1 Intervention
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.
Group II: Standard Services OnlyActive Control1 Intervention
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.
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Who is running the clinical trial?
RTI InternationalLead Sponsor
196 Previous Clinical Trials
841,546 Total Patients Enrolled
Marni Kan, PhDStudy DirectorRTI International
Alexandra Minnis, PhDPrincipal InvestigatorRTI International
1 Previous Clinical Trials
400 Total Patients Enrolled
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