Caregiver-Adolescent Dating Violence Prevention Intervention Pilot Trial
This pilot study is testing a program called FLARE, which aims to prevent dating violence among sexual and gender diverse youth (SGDY) and their trusted adults. FLARE involves in-person and online activities. We are looking for 108 participants, including youth aged 14-18 who identify as sexually or gender diverse, speak English, and can travel to Pittsburgh for one event. They also need a caregiver (18 or older) to participate. The study will compare FLARE to a resource guide, with the resource guide group getting access to FLARE later. We want to see if FLARE is acceptable and practical, and if it helps with behavioral changes. The study's current status is unclear.
- Study design
- This is an interventional pilot trial with 108 planned participants. It compares the FLARE program to a control group that receives a resource guide.
- What's involved
- You would participate in a program over a 4-week period, including one full day in-person session, two virtual group sessions, and online activities. You would also complete assessments at baseline, 1 month, and 3 months.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for 3 months after the initial baseline assessment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Caregiver-Adolescent Dating Violence Prevention Intervention Pilot Trial
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Maya I Ragavan · PRINCIPAL_INVESTIGATOR · University of Pittsburgh
- Robert Coulter · PRINCIPAL_INVESTIGATOR · University of Pittsburgh
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- AcceptabilityT2 (1 month post baseline)
Acceptability of Intervention Measure: Mean value of 4 items. Each question uses a five-point Likert scale for responses, coded with a value from 1 (Completely disagree) to 5 (Completely agree) and averaged to produce the mean value. The higher the computed mean value, the greater acceptability of the intervention.
- Trial FeasibilityT1 (baseline); T2 (1 month post baseline); T3 (3 months post baseline, 2 months post T2)
Trial Consent Rate: % of individuals who assented/consented to participate out of individuals who screened eligible Trial Baseline Participation Rate: % of individuals who completed the baseline survey out of individuals who assented/consented to participate Trial Intervention Demand: % of intervention arm participants who complete the intervention Trial Retention Rate: % of participants who complete each followup survey