What this study is
Youth of color, particularly in urban communities, face disproportionate anxiety levels due to systemic inequities, including exposure to violence, economic instability, and neighborhood disadvantage. Despite increased need, these communities often lack accessible, culturally relevant mental health interventions. This study presents a protocol for a community-driven anxiety prevention intervention tailored to urban youth of color using community-based participatory research (CBPR) methods. The intervention, co-developed with community partners and youth includes five structured weekly sessions on psychoeducation, coping skills, and role-playing exercises. Facilitators trained in social work or psychology will deliver the intervention, with at least one facilitator from the target community ensuring cultural relevance. Recruitment will occur through collaboration with a local high school, with counselors identifying high-risk youth. Data from pilot interventional trial will be collected at baseline, post-intervention, and a three-month follow-up using validated measures such as the Generalized Anxiety Disorder-7 (GAD-7) scale. This study highlights community-based participatory research approach in addressing mental health disparities among urban youth. By incorporating community perspectives, the intervention ensures cultural alignment. Findings will inform future adaptations of community centered anxiety interventions and contribute to knowledge on improving mental health accessibility for marginalized youth. If effective, this model could be expanded to support youth in other under-resourced communities.
What's being tested
- Anxiety Prevention Intervention
Intervention · BEHAVIORAL
community and school based, delivered by peers from the community to educate and lower anxiety symptoms among youth
- Anxiety Intervention
Intervention · BEHAVIORAL
5-session social and behavioral intervention about managing anxiety symptoms
Study details
- Official title
- Paterson Prevention Project Anxiety Prevention Intervention
- Sponsor
- Yale University
- Conditions
- Moderate Anxiety
- Enrolling
- 50 people
- Starts
- 2025-05-07
- Est. completion
- 2025-08-30
- Design
- Open-label, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 13 Years – 21 YearsSex ALLHealthy volunteers AcceptedYou may qualify if
- Able to speak and read in English
- Reside in Paterson
You can't join if
- English is not first language and cannot read or write English
- Does not have residence in Paterson
- Has not provided consent to participate in study
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openPaterson College Achieve High School
Paterson, New Jersey, United States
Study team
Sponsor
Yale University
Study ID 2000030293
Principal investigator
Ijeoma Opara, PhD
Yale University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.