Anxiety Disorders Clinical Trial
Official title:
CRISOL Mente: A Multilevel Community Intervention to Reduce Mental Health Disparities Among Latinos
Verified date | November 2023 |
Source | Drexel University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Latinos in the U.S. experience significant disparities in access to mental health services due to lack of health insurance, language barriers, low availability of bilingual providers, mental health stigma, and fear of deportation. There is an urgent need to identify low-cost, culturally appropriate interventions to reduce mental health disparities among this population. This project will address that need by implementing and testing CRISOL Mente, a multi-level, culturally-congruent community intervention to improve the mental health of the Latino population in Philadelphia.
Status | Recruiting |
Enrollment | 600 |
Est. completion date | August 31, 2027 |
Est. primary completion date | August 31, 2027 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Ages 18-65 - Fluent in English or Spanish - Self-identification as a member of the Latino community - Resident of Philadelphia, Bucks, Montgomery, Delaware, or Chester County. - Moderate to severe clinical symptoms of anxiety, depression, and/or PTSD Exclusion Criteria: - People with high-risk mental health symptoms: active suicidality, substance use disorder, mania, psychosis, and schizophrenia - People already receiving mental health therapy (in the last 3 months) - Pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | Drexel University School of Public Health | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Drexel University | Esperanza Health Center, The Philadelphia AIDS Consortium |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Improvement in mental health symptomatology (depressive, anxiety or post-traumatic stress disorder [PTSD]) | Clinically meaningful improvement in symptomatology of at least one of depressive, anxiety symptoms and/or PTSD (composite primary outcome) from baseline to the end of 6 months of treatment.
Where improvement is defined as: Epidemiologic Studies Depression Scale Revised (CESD-R10) decline of >=30% in the overall score or scoring below the cutoff for depressive disorder, and/or General Anxiety Disorder-7 (GAD-7) decline of >=30% in the overall score or scoring below the cutoff for anxiety disorder, and/or PTSD decline of >=30% in the overall score or scoring below the cutoff for PTSD |
Baseline to 6 months | |
Secondary | Depressive symptomatology | Presence or absence of any clinical mental health disorder will be determined using Center for Measured using Epidemiologic Studies Depression Scale Revised (CESD-R10) for depressive symptoms (continuously) | Baseline to 6 months | |
Secondary | Anxiety symptomatology | Measured using General Anxiety Disorder-7 (GAD-7) scale for anxiety symptoms (continuosly) | Baseline to 6 months | |
Secondary | Post traumatic stress disorder symptomatology | Measured using the Short Screening Scale for post-traumatic stress disorder (PTSD). | Baseline to 6 months |
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