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Clinical Trials/NCT00227929
NCT00227929
Completed
N/A

Effectiveness of Culturally Sensitive Collaborative Treatment (CSCT) of Depressed Chinese Americans in Primary Care

Massachusetts General Hospital1 site in 1 country120 target enrollmentJuly 2003
ConditionsDepression

Overview

Phase
N/A
Intervention
Not specified
Conditions
Depression
Sponsor
Massachusetts General Hospital
Enrollment
120
Locations
1
Primary Endpoint
Symptoms of depression; measured at Weeks 2, 6, 10, 14, 18, 22, and 24
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This study will evaluate the effectiveness of culturally sensitive treatment versus regular care in treating depressed Chinese Americans.

Detailed Description

Depression is a complex illness that impacts an individual's thoughts, behavior, mood, and physical health. Research has shown that many Asian Americans with depression do not complain about their symptoms or seek treatment, which has lead to an under-recognition of depression in this population. Furthermore, even when a primary care physician does diagnose depression in an Asian American, adequate treatment does not often follow. There is a clear need to understand the cultural reasons for why treatment is not sought out by Asian Americans. There is also a need for developing new treatments that specifically target the Asian American population. Offering culturally sensitive therapies combined with traditional medical care may make depressed Asian Americans more comfortable in seeking treatment for their illness. Culturally Sensitive Collaborative Treatment (CSCT) is a comprehensive approach to treating depression. It incorporates consultation with a culturally trained psychiatrist, medical treatment provided by a primary care provider, and care management provided by a bilingual and bicultural care manager. The purpose of this study is to evaluate the effectiveness of CSCT versus traditional medical care for the treatment of depression in Chinese Americans. This 24-week study will enroll depressed Chinese Americans. Potential participants will be interviewed in primary care clinics to screen for depression. Once enrolled, all participants will attend a consultation with a psychiatrist trained in cultural sensitivity to introduce the concept and treatment of depression. Participants will then be randomly assigned to either CSCT or standard care. Both groups of participants will receive regular care from their primary care provider, but the CSCT group will also meet with a bilingual and bicultural care manager to learn how to fully manage their depression. Outcome measurements will include symptoms of depression; adherence to appointments with primary care providers; adherence to medication treatment; and adverse events. All measurements will be assessed during follow-up phone calls at Weeks 2, 6, 10, 14, 18, 22, and 24.

Registry
clinicaltrials.gov
Start Date
July 2003
End Date
June 2008
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Albert Yeung

Staff Psychiatrist

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Chinese ethnicity
  • Currently depressed as determined by a total score of at least 16 on the CBCI scale
  • Speaks and understands English or Chinese (including Mandarin, Cantonese, and Taiwanese dialect)
  • Willing to participate in follow-up phone calls

Exclusion Criteria

  • Currently at risk for suicide
  • Current unstable medical illness
  • Current clinical or laboratory evidence of hypothyroidism
  • Diagnosed with any of the following in addition to depression: organic mental disorder; schizophrenia; delusional disorder; psychotic disorder; bipolar disorder; mood congruent or mood incongruent psychotic features
  • History of treatment by a psychiatrist within 4 months of study entry
  • History of alcohol or substance abuse within 1 year of study entry

Outcomes

Primary Outcomes

Symptoms of depression; measured at Weeks 2, 6, 10, 14, 18, 22, and 24

Secondary Outcomes

  • Quality of life; measured at Weeks 2, 6, 10, 14, 18, 22, and 24
  • Adherence to clinic visits with the primary care physicians; measured at Weeks 2, 6, 10, 14, 18, 22, and 24
  • Adverse events; measured at Weeks 2, 6, 10, 14, 18, 22, and 24
  • Adherence to medication treatment; measured at Weeks 2, 6, 10, 14, 18, 22, and 24

Study Sites (1)

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