MedPath

Step 1: Be Aware, Anxiety Prevention Intervention

Not Applicable
Conditions
Moderate Anxiety
Registration Number
NCT07044752
Lead Sponsor
Yale University
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
All
Target Recruitment
50
Inclusion Criteria
  • able to speak and read in English
  • reside in Paterson
Exclusion Criteria
  • 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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Generalized Anxiety Disorder30 days

Symptoms of Anxiety, Mild, Moderate, Severe

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Paterson College Achieve High School

🇺🇸

Paterson, New Jersey, United States

Paterson College Achieve High School
🇺🇸Paterson, New Jersey, United States
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