Pilot Trial of Clinic-based Dating Violence Prevention Program for Adolescents and Caregivers
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Engaging Together for Health Relationships.
- Who it may be relevant to
- Registry conditions: Dating Violence, Parent, Primary Care. Basic parameters: from 12 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Engaging Together for Healthy Relationships Version 2.0: Multisite Pilot Intervention Trial
Overview
ETHR V 2.0 pilot trial is a one-arm, multi-site pilot trial to assess the acceptability and feasibility of Engaging Together for Healthy Relationships, a caregiver-adolescent dating violence prevention program delivered within pediatric primary care.
Detailed description
ETHR V 2.0 pilot trial is a one-arm (intervention only) pilot trial of Engaging Together for Healthy Relationships, a caregiver-adolescent dating violence prevention program delivered within pediatric primary care. We completed one round of the pilot trial in two clinics in Pittsburgh and now are expanding the trial to include two sites with all providers in each site. ETHR includes clinician training, in-clinic resources, and after visit text messages and resources for families. This is an intervention only trial to assess acceptability, feasibility, and exploratory pre/post changes in outcomes.
Interventions
- Behavioral Engaging Together for Health Relationships
Dating violence intervention for caregivers and adolescents to be delivered within pediatric primary care
Primary outcome measures
- Percentage of participants who are eligible out of the total who are approached [Time frame: Through completion of study recruitment, an average of 6 months]
- Percentage of participants who are consented out of the total who are eligible [Time frame: Through completion of study recruitment, an average of 6 months]
- Percentage of participants who complete the baseline survey out of the total who consented [Time frame: Through completion of completing baseline surveys, an average of 6 months]
- Percentage of participants who complete the well-visit out of the total who consented [Time frame: Through completion of completing well-visits, an average of 6 months]
- Percentage of participants who complete the immediate post-intervention survey out of the total who consented [Time frame: Through completion of completing post-intervention survey, an average of 7 months]
- Percentage of participants who complete the 1-month post-intervention survey out of the total who consented [Time frame: 4 months]
- Percentage of participants who complete the 3-month post-intervention survey out of the total who consented [Time frame: Through completion of completing 3 month post-intervention survey, an average of 12 months]
- Percentage of participants who strongly agree or agree that the intervention is acceptable using a 4-item validated measure (Acceptability of Intervention Measure) [Time frame: Through completion of completing immediate post-visit surveys, an average of 6 months]
- Percent of participants who received intervention during pediatric primary care visit [Time frame: Through completion of completing well-visits, an average of 6 months]
- Participants use intervention resources after the visit [Time frame: Through completion of intervention, on average 3 months post well visit]
Secondary outcome measures (8)
- Self-efficacy in preventing adolescent relationship abuse (ARA), change in outcome between baseline and 3 months [Time frame: Baseline, 3-month post intervention]
- Percentage of participants who utilize ARA resources at each measurement point, change in outcome over time [Time frame: Baseline, 1 month post intervention, 3 month post-intervention]
- Attitudes about ARA, change in outcome between baseline and 3 months [Time frame: Baseline, 3-month post intervention]
- Motivation around preventing dating violence [Time frame: Baseline, 3-month post intervention]
- Parent-adolescent communication around dating and ARA, change in outcome over time [Time frame: Baseline, 3-month post intervention]
- Parental monitoring around dating and ARA, change in outcome over time [Time frame: Baseline, 3-month post intervention]
- Percentage of adolescents reporting ARA victimization and perpetration [Time frame: Baseline, 3-month post intervention]
- ARA knowledge [Time frame: baseline, 3 months surveys (6 months total)]
Eligibility criteria
Inclusion criteria
Providers:
- Sees patient at an eligible primary care clinic
- Speaks and understands English
- Age 18 or older
- Identifies as a pediatrician, nurse practitioner, physician assistant (pediatric primary care healthcare provider)
Adolescents
- Age 12 to 16
- Attending an upcoming well-child visit from a provider enrolled in the study
- Caregiver who is accompanying well-child visit with adolescent is also participating
- Speaks and understands English
Parents
- Is parent or primary caregiver for an adolescent age 12 to 16
- Adolescent has an upcoming well-child visit with a provider enrolled in the study
- Accompanying child to the well-visit
- Adolescent is interested and eligible to participate in study
- Speaks and understand English
Exclusion criteria
- Unable to assent/consent
- Does not meet inclusion criteria
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Prevention
Study locations
United States · 1 center
- UPMC Children's Community Practice — Monongahela
Identifiers
NCT: NCT07039253 · STUDY25030017 · 1R21HD109627-01A1