Effectiveness of Cultural Sensitive Collaborative Treatment of Depressed Chinese

This study has been completed.
Sponsor:
Collaborator:
National Health Research Institutes, Taiwan
Information provided by (Responsible Party):
Shen-Ing,Liu, Mackay Memorial Hospital
ClinicalTrials.gov Identifier:
NCT00664885
First received: April 18, 2008
Last updated: January 8, 2014
Last verified: January 2014
  Purpose

This study is a randomized controlled trial to test whether Culturally Sensitive Collaborative Treatment (CSCT) would improve the outcome of depressed patients visiting non-psychiatric settings in Taiwan.


Condition Intervention
Depression
Other: Culturally Sensitive Collaborative Treatment

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Effectiveness of Cultural Sensitive Collaborative Treatment of Depressed Chinese in Primary Care

Resource links provided by NLM:


Further study details as provided by Mackay Memorial Hospital:

Primary Outcome Measures:
  • Depressed patients who receive CSCT have improved treatment outcomes compared to patients who receive usual care. [ Time Frame: 2wk,6 wk,10 wk,14 wk,18 wk,22wk,26wk ] [ Designated as safety issue: Yes ]

Enrollment: 280
Study Start Date: January 2008
Study Completion Date: December 2012
Primary Completion Date: March 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: CSCT Other: Culturally Sensitive Collaborative Treatment
a collaborative care model, for treating depressed patients in general medical care

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients who attend non-psychiatric clinics at the above site.
  • Patients with Major Depressive Disorder (MDD), defined as a positive screen using the PHQ-9, confirmed with the SCAN interview.
  • Men or women aged 18 or older.
  • Able to participate in a clinical diagnostic interview in either Mandarin or Fukienese dialects.
  • Individuals who are willing to be followed up concerning their depression symptoms.
  • Individuals who have completed a written consent form.

Exclusion Criteria:

  • Women who are pregnant, breast-feeding, or planning pregnancy within the next year.
  • Patients with serious suicidal risk.
  • Patients with unstable medical illnesses.
  • Clinical or laboratory evidence of hypothyroidism.
  • Patients with comorbid severe mental disorders
  • Patients with history of treatment by a psychiatrist in the past 4 months.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00664885

Locations
Taiwan
Mackay Memorial Hospital
Taipei, Taiwan, 251
Sponsors and Collaborators
Mackay Memorial Hospital
National Health Research Institutes, Taiwan
  More Information

No publications provided

Responsible Party: Shen-Ing,Liu, Department of Psychiatry, Mackay Memorial Hospital
ClinicalTrials.gov Identifier: NCT00664885     History of Changes
Other Study ID Numbers: NHRI-EX97-9706PI
Study First Received: April 18, 2008
Last Updated: January 8, 2014
Health Authority: Taiwan: Department of Health

Keywords provided by Mackay Memorial Hospital:
non-psychiatric
clinics

Additional relevant MeSH terms:
Depression
Depressive Disorder
Behavioral Symptoms
Mood Disorders
Mental Disorders

ClinicalTrials.gov processed this record on July 28, 2014