Pilot Trial of Dating Violence Prevention Program for Adolescents and Caregivers

This study is testing a program called "Engaging Together for Healthy Relationships" (ETHR) which aims to prevent dating violence. It's designed for adolescents (ages 12-16) and their caregivers, and will be delivered during regular check-ups at pediatric primary care clinics. The main goal is to see if the program is acceptable and practical to use in these clinics. Researchers will measure how many eligible people are approached, how many agree to join, and how many complete the initial surveys. This study plans to enroll 120 participants and is currently expanding to include more clinics.

Study design
This is a single-arm pilot study, meaning all participants will receive the ETHR program. It aims to enroll 120 participants.
What's involved
Participants will attend an upcoming well-child visit where the program will be delivered, and may receive after-visit text messages and resources. Baseline surveys will be completed within approximately 6 months.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoints are measured through the completion of study recruitment and baseline surveys, which is an average of 6 months.

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NCT07039253

Pilot Trial of Clinic-based Dating Violence Prevention Program for Adolescents and Caregivers

Recruiting
NAAges 12+InterventionalPrevention
University of Pittsburgh
~120 participants
Updated 2026-06-04 on ClinicalTrials.gov
What's tested:Engaging Together for Health Relationships

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percentage of participants who are eligible out of the total who are approached
Measured over Through completion of study recruitment, an average of 6 months
+9 more outcomes measured
Dating Violence
Parent
Primary Care
1 sites across 1 states
Pennsylvania1
  • Maya Ragavan, MD, MPH, MS · PRINCIPAL_INVESTIGATOR · University of Pittsburgh

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Eligibility criteria

Exclusion

Unable to assent/consent
  • Percentage of participants who are eligible out of the total who are approachedThrough completion of study recruitment, an average of 6 months

    Will assess through tracking data

  • Percentage of participants who are consented out of the total who are eligibleThrough completion of study recruitment, an average of 6 months

    Will assess through tracking data

  • Percentage of participants who complete the baseline survey out of the total who consentedThrough completion of completing baseline surveys, an average of 6 months

    Will assess through tracking data

  • Percentage of participants who complete the well-visit out of the total who consentedThrough completion of completing well-visits, an average of 6 months

    Will assess through tracking data

  • Percentage of participants who complete the immediate post-intervention survey out of the total who consentedThrough completion of completing post-intervention survey, an average of 7 months

    Will assess through tracking data

  • Percentage of participants who complete the 1-month post-intervention survey out of the total who consented4 months

    Through completion of completing 1- month post-intervention survey, an average of 8 months

  • Percentage of participants who complete the 3-month post-intervention survey out of the total who consentedThrough completion of completing 3 month post-intervention survey, an average of 12 months

    Will assess through tracking data

  • Percentage of participants who strongly agree or agree that the intervention is acceptable using a 4-item validated measure (Acceptability of Intervention Measure)Through completion of completing immediate post-visit surveys, an average of 6 months

    Validated measure (Acceptability of Intervention Measure)

  • Percent of participants who received intervention during pediatric primary care visitThrough completion of completing well-visits, an average of 6 months

    Investigator-developed measure with questions about what components of the intervention were received during the well visit

  • Participants use intervention resources after the visitThrough completion of intervention, on average 3 months post well visit

    Investigator-developed measure on use of intervention resources after the visit