Culturally Sensitive Depression Care Management for Latino Primary Care Patients

Depression Clinical Trial

Official title:

Culturally Sensitive Depression Care Management for Latino Primary Care Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00571454
• Other study ID #: RWJ
• Status: Completed
• Phase: Phase 2
• First received: December 10, 2007
• Last updated: October 28, 2009
• Start date: May 2007
• Est. completion date: August 2008

Study information

• Verified date: October 2009
• Source: Butler Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether telephonic depression care management can improve depression outcomes for Latino primary care patients who are enrolled in Medicaid and are receiving an antidepressant from their primary care doctor.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 38
• Est. completion date: August 2008
• Est. primary completion date: August 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Latino

• Adult

• Received an antidepressant prescription from primary care provider

• Not current receiving care from behavioral health provider

• Diagnosis of major depression, minor depression, dysthymia, or significant depression symptoms

• English or Spanish speaking

• Member, Neighborhood Health Plan of RI

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Health Services Research

Related Conditions & MeSH terms

• Depression
• Depressive Disorder

Intervention

Behavioral:
• telephone depression care management
1 call per week for first 4 weeks 1 call every other week for next 8 weeks

Locations

Country	Name	City	State
United States	Neighborhood Health Plan of RI	Providence	Rhode Island

Sponsors (4)

Lead Sponsor	Collaborator
Butler Hospital	Beacon Health Strategies, Neighborhood health Plan of RI, Robert Wood Johnson Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quick Inventory of Depressive Symptomatology - Clinician Administered (QIDS-C)		3 months	No
Secondary	Center for Epidemiological Studies-- Depression		3 months	No
Secondary	WHO Disability Assessment Schedule (WHO-DAS)		3 months	No
Secondary	Treatment Utilization		3 months	No
Secondary	Treatment Satisfaction		3 months	No
Secondary	costs: health care utilization		3 months	No