Engaging Together for Healthy Relationships
BehavioralA comprehensive parent-adolescent dating violence prevention intervention designed to be provider delivered within the context of a pediatric well-child visit
NCT Number: NCT05880979
The goal of this pilot randomized clinical trial is to assess feasibility and acceptability of a brief parent-adolescent dating violence prevention intervention (Engaging Together for Healthy Relationships; ETHR) delivered in pediatric primary care settings. The main questions it aims to answer is if ETHR is acceptable and feasible. 4 healthcare providers will receive ETHR to share with their patients which includes clinician training, provider-delivered scripts, resource guides, and a comprehensive website. This will be compared to providers conducting routine well-child care with their patients.
Looking for future studies?
Notify Me11 year and older
All sexes
Interventional
Not applicable
CCP South Hills, Monongahela, Pennsylvania, United States
The investigators are conducting a pilot randomized clinical trial to test a brief parent-adolescent dating violence prevention intervention (Engaging Together for Healthy Relationships; ETHR). ETHR has been developed for parents and adolescents, to be implemented within pediatric primary care settings. ETHR is a comprehensive intervention which includes a training for clinicians, brief educational scripts for providers, resource guides for the adolescent, parent, and dyad, a comprehensive website, and warm referral processes to connect families with local resources. The investigators will be comparing ETHR with routine care. The specific goal of the pilot trial is to test trial feasibility, as well as intervention acceptability and fidelity. The investigators also will be examining exploratory changes in secondary outcomes and early implementation barriers and facilitators.
Four pediatric clinics will participate in this study. The investigator will recruit two providers from each clinic and randomize them into the intervention provider or control provider. The intervention provider will receive ETHR and the control provider will complete their regular well-child care. The investigators will enroll 15 families in the intervention arm and 5 in the control arm (3:1 enrollment). Families who are seeing the intervention provider for a well-child visit will be enrolled in the intervention arm; those seeing the control provider will be enrolled in the control arm. Families will be eligible if they are seeing the intervention or control providers for a well child visit, if the adolescent coming for the well-visit is between 11 to 15, if both the caregiver and adolescent are interested in participating, and if the family speaks and understands English. Families will be called 2 weeks ahead of their visit to enroll, consent, and complete a baseline survey (both the adolescent and parent will complete the survey). Participants will then attend their well -visit (where they will receive ETHR or routine care, depending on their provider). They will complete an acceptability and fidelity survey immediately post-visit, a resource utilization survey 1 month post visit, and a follow up survey (identical to the baseline survey) 3 months post visit. Providers will complete a brief fidelity and acceptability survey after each study visit (15 for intervention providers, 5 for control providers). All providers and a subset of families enrolled in the intervention arm (20 dyads, 40 participants) will also complete post-intervention interviews.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Providers:
Adolescents
Parents
Exclusion criteria
Providers
A comprehensive parent-adolescent dating violence prevention intervention designed to be provider delivered within the context of a pediatric well-child visit
Participants will receive their regularly scheduled well-child care
Time frame: Through completion of study recruitment, an average of 6 months
Will assess through tracking data
Time frame: Through completion of study recruitment, an average of 6 months
Will assess through tracking data
Time frame: Through completion of completing baseline surveys, an average of 6 months
Will assess through tracking data
Time frame: Through completion of completing well-visits, an average of 6 months
Will assess through tracking data
Time frame: Through completion of completing post-intervention survey, an average of 7 months
Will assess through tracking data
Time frame: 4 months
Through completion of completing 1- month post-intervention survey, an average of 8 months
Time frame: Through completion of completing 3 month post-intervention survey, an average of 12 months
Will assess through tracking data
Time frame: Through completion of completing immediate post-visit surveys, an average of 6 months
Validated measure (Acceptability of Intervention Measure)
Time frame: Baseline, 3-month post intervention
Self-efficacy around ARA prevention, 1-5 scale (5=higher self-efficacy)
Time frame: Baseline, 1 month post intervention, 3 month post-intervention
Investigator developed measure (yes/no)
Time frame: Baseline, 3-month post intervention
Attitudes about Abusive Relationships, 1-5 scale (1=not abusive, 5=very abusive)
Time frame: Baseline, 3-month post intervention
Investigator developed measure, yes/no answer choices (yes=has communicated, no=has not communicated)
Time frame: Baseline, 3-month post intervention
Parenting Practices Scale (never to always; 1=never, 5=always)
Time frame: Baseline, 3-month post intervention
CADRI Short Form 1-5 scale (never to everyday)
University of Pittsburgh
Other
Engaging Together for Healthy Relationships: A Pilot Trial to Test a Brief Dating Violence Prevention Intervention for Pediatric Primary Care
Acronym: ETHR
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04850274
Behavior, Chemically-Induced Disorders
Atlanta, Georgia, United States
View Trial DetailsNCT05821205
Violence in Adolescence
Ann Arbor, Michigan, United States
View Trial DetailsNCT05240313
Alcohol Drinking, Behavior
Doral, Florida, United States
View Trial DetailsNCT05185453
Adolescent Behavior, Behavior
Pittsburgh, Pennsylvania, United States
View Trial Details