NCT00260169

Brief Summary

This study will determine ways to make depression care more responsive to the needs of consumers in primary care clinics serving low-income Latinos.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
432

participants targeted

Target at P75+ for not_applicable depression

Timeline
Completed

Started Nov 2005

Typical duration for not_applicable depression

Geographic Reach
1 country

3 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2005

Completed
28 days until next milestone

First Submitted

Initial submission to the registry

November 29, 2005

Completed
2 days until next milestone

First Posted

Study publicly available on registry

December 1, 2005

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2007

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2009

Completed
Last Updated

December 10, 2013

Status Verified

December 1, 2013

Enrollment Period

1.9 years

First QC Date

November 29, 2005

Last Update Submit

December 9, 2013

Conditions

Keywords

Treatment PreferencesPublic sectorLatino

Outcome Measures

Primary Outcomes (1)

  • Depression treatment preferences as measured by a conjoint analysis survey and qualitative interviews

    Measured at Week 16

Secondary Outcomes (1)

  • Depression outcomes as measured by the Patient Health Questionnaire-9

    Measured at Week 16

Study Arms (2)

1

EXPERIMENTAL

Participants will receive collaborative care

Behavioral: Collaborative care treatment

2

ACTIVE COMPARATOR

Participants will receive enhanced usual care

Behavioral: Enhanced usual care

Interventions

Patients receiving collaborative care treatment choose 12 weeks of CBT and/or medication management (antidepressants prescribed by patients' primary care provider) from the study depression care specialist (DCS).

1

Usual care participants are assigned to a 16-week wait-list for the study treatment, during which they are free to receive treatment elsewhere. A letter is given to participants' primary care providers (PCP) that indicates they screened positive for depression. In addition, patients receive an information booklet about depression and a community resource list.

2

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • For Participating Patients:
  • Attending one of the study clinics for primary care
  • English or Spanish-speaking
  • Screens positive for major depressive disorder or dysthymia
  • For Providers:
  • All primary care providers providing at least one day of services at one of the study clinics
  • For Administrators:
  • Administrative, medical, and nursing directors from each study site and directors of affiliated local mental health clinics

You may not qualify if:

  • For Participating Patients:
  • Acutely suicidal
  • Screens positive for bipolar disorder, psychotic disorder, or cognitive impairment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

H. Claude Hudson Comprehensive Health Center

Los Angeles, California, 90007, United States

Location

USC Family Practice Center at California Hospital

Los Angeles, California, 90015, United States

Location

LAC+USC Outpatient Department

Los Angeles, California, 90033, United States

Location

Related Publications (1)

  • Dwight-Johnson M, Lagomasino IT, Hay J, Zhang L, Tang L, Green JM, Duan N. Effectiveness of collaborative care in addressing depression treatment preferences among low-income Latinos. Psychiatr Serv. 2010 Nov;61(11):1112-8. doi: 10.1176/ps.2010.61.11.1112.

MeSH Terms

Conditions

Depression

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Study Officials

  • Isabel T. Lagomasino, MD, MSHS

    University of Southern California

    PRINCIPAL INVESTIGATOR
  • Megan Dwight-Johnson, MD, MPH

    VA Medical Center-West Los Angeles

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Study Principal Investigator

Study Record Dates

First Submitted

November 29, 2005

First Posted

December 1, 2005

Study Start

November 1, 2005

Primary Completion

October 1, 2007

Study Completion

January 1, 2009

Last Updated

December 10, 2013

Record last verified: 2013-12

Locations