Chicago Urban Resiliency Building (CURB)

• Register: ClinicalTrials.gov
• Last refreshed on: 10 August 2015
• Main ID: NCT01571011
• Date of registration: 20/03/2012
• Prospective Registration: No
• Primary sponsor: Benjamin Van Voorhees, MD, MPH
• Public title: Chicago Urban Resiliency Building (CURB) CURB
• Scientific title: Chicago Urban Resiliency Building (CURB): Phase 3 Clinical Trial in Primary Care to Engage Adolescents With a Web-based Depression Prevention Intervention
• Date of first enrolment: March 2012
• Target sample size: 10
• Recruitment status: Completed
• URL: https://clinicaltrials.gov/show/NCT01571011
• Study type: Interventional
• Study design: Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention
• Phase: N/A

Countries of recruitment

United States

Contacts

• Name: Benjamin Van Voorhees, MD, MPH
• Affiliation: University of Illinois at Chicago

• Name: Monika Marko, MSS
• Affiliation: UIS

Key inclusion & exclusion criteria

Inclusion Criteria:

Adolescents:

- Male and female African American and Latino/a youth ages 13 -17 years old.

- Adolescents with depressed mood (> 2 weeks duration) will be eligible unless they
have already exceeded the diagnostic threshold for major depressive disorder or have
a comorbid condition as defined in the exclusion criteria.

Parents:

- Parent of eligible adolescents

Primary Care Physicians (PCPs):

- Physician at one of the four Mile Square Health Centers.

Health Care Professionals:

- Employee at one of the four Mile Square Health Centers.

Exclusion Criteria:

- Adolescents undergoing active treatment for depression [Active treatment for
depression is defined as receiving anti-depressant medication or counseling within
one year of remission of symptoms from the most recent episode]

- Adolescents meeting probable diagnostic criteria for the following: Major depression,
Substance and alcohol abuse, Panic attacks, Generalized anxiety disorder, Eating
disorders, History of treatment for bi-polar disorder or schizophrenia or who are at
elevated risk for suicide (often have suicidal thoughts or recent intent)



Age minimum: 13 Years
Age maximum: 17 Years
Gender: Both

Health Condition(s) or Problem(s) studied

Major Depression

Intervention(s)

Behavioral: CURB

Primary Outcome(s)

The Center for Epidemiological Studies of Depression (CES-D) Scale [Time Frame: 0, 3, 6 months]

Secondary Outcome(s)

Cost effective outcome measures [Time Frame: 6 months]

Protective factors [Time Frame: 6 months]

Vulnerability [Time Frame: 6 months]

Secondary ID(s)

RWJF 68177

Source(s) of Monetary Support

Please refer to primary and secondary sponsors