N/A
Completed N=175
Emergency Department Healthcare Education Assessment and Response for Teen Relationships: A Pilot Feasibility Study
Adolescent Behavior · Emergency Department · Abuse Physical · Abuse Mental
Source: ClinicalTrials.gov NCT05194202 ↗
Enrolled (actual)
175
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcomePrimary: Participant Acceptability Ratings for Healthcare Provider Discussions on Relationships in ED-Heart Intervention Arm — 39; 6 Participants — p=.622
Summary
This is a single-site, randomized, controlled trial. Investigators will evaluate feasibility of the Emergency Department Healthcare Education Assessment and Response for Teen Relationships (ED-HEART) intervention among adolescents age 14-19 years receiving care in the Children's Mercy emergency department.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Participant Acceptability Ratings for Healthcare Provider Discussions on Relationships in ED-Heart Intervention Arm |
39; 6 | .622 |
| PRIMARY Participant Acceptability Ratings for ED-based Relationship Intervention in ED-Heart Intervention Arm |
34; 11 | .038 sig |
| SECONDARY ARA Victimization |
1; 5 | — |
| SECONDARY Recognition of Abusive Behaviors |
4.18; 4.26 | — |
Eligibility Criteria
Inclusion Criteria
- emergency department (ED) patient 14-19 years of age.
Exclusion Criteria
- Developmental delay, severe illness, or cognitive impairment precluding informed consent/assent or completion of study activities, as determined by ED team or study team.
- Current ED evaluation for acute sexual assault/abuse.
- Current mental or behavioral health symptoms precluding completion of study activities, as determined by ED team or study team.
- Caregiver declines to step out to allow assent/consent in private or adolescent declines for caregiver to step out to allow assent/consent or participation in private.
- Adolescent is non-English speaking.
- Parent is non-English or non-Spanish speaking.
Data sourced from ClinicalTrials.gov (NCT05194202). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.